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<meta name="description" content="We show that SAMD9 is an innate host antiviral stress response element that participates in the formation of antiviral granules. Poxviruses, myxoma virus and vaccinia virus specifically, utilize a virus-encoded host range factor(s), such as a member of the C7L superfamily, to antagonize SAMD9 to pre …"><meta name="keywords" content="pmid:25428864, PMC4300762, doi:10.1128/JVI.02262-14, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov&#x27;t, Jia Liu, Grant McFadden, Antiviral Agents / metabolism*, HeLa Cells, Humans, Immunity, Innate*, Intracellular Signaling Peptides and Proteins, Poxviridae / immunology*, Proteins / metabolism*, PubMed Abstract, NIH, NLM, NCBI, National Institutes of Health, National Center for Biotechnology Information, National Library of Medicine, MEDLINE"><meta name="robots" content="index,nofollow,noarchive"><meta property="og:title" content="SAMD9 is an innate antiviral host factor with stress response properties that can be antagonized by poxviruses - PubMed"><meta property="og:url" content="https://pubmed.ncbi.nlm.nih.gov/25428864/"><meta property="og:description" content="We show that SAMD9 is an innate host antiviral stress response element that participates in the formation of antiviral granules. Poxviruses, myxoma virus and vaccinia virus specifically, utilize a virus-encoded host range factor(s), such as a member of the C7L superfamily, to antagonize SAMD9 to pre …"><meta property="og:image" content="https://cdn.ncbi.nlm.nih.gov/pubmed/persistent/pubmed-meta-image-v2.jpg"><meta property="og:image:secure_url" content="https://cdn.ncbi.nlm.nih.gov/pubmed/persistent/pubmed-meta-image-v2.jpg"><meta property="og:type" content="website"><meta property="og:site_name" content="PubMed"><meta name="twitter:domain" content="pubmed.ncbi.nlm.nih.gov"><meta name="twitter:card" content="summary_large_image"><meta name="twitter:title" content="SAMD9 is an innate antiviral host factor with stress response properties that can be antagonized by poxviruses - PubMed"><meta name="twitter:url" content="https://pubmed.ncbi.nlm.nih.gov/25428864/"><meta name="twitter:description" content="We show that SAMD9 is an innate host antiviral stress response element that participates in the formation of antiviral granules. Poxviruses, myxoma virus and vaccinia virus specifically, utilize a virus-encoded host range factor(s), such as a member of the C7L superfamily, to antagonize SAMD9 to pre …"><meta name="twitter:image" content="https://cdn.ncbi.nlm.nih.gov/pubmed/persistent/pubmed-meta-image-v2.jpg">
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<option selected="selected" value="summary">Summary</option>
<option value="summary-text">Summary (text)</option>
<option value="abstract">Abstract</option>
<option value="abstract-text">Abstract (text)</option>
</select>
</div>
<div class="include-supplemental-container">
<input type="checkbox" aria-label="Include MeSH and other data" name="include-supplemental" id="email-include-supplemental" class="email-include-supplemental">
<label for="email-include-supplemental" class="email-include-supplemental-label">MeSH and other data</label>
</div>
<div class="form-field recaptcha ">
<div class="g-recaptcha" id="id-recaptcha" data-sitekey="6LfsWHMdAAAAAClKbtOpjQ2pMjgsGxvv7NdZW9uI"></div>
</div>
<div id="captcha-error-message" class="usa-input-error-message captcha-validation-message" role="alert"></div>
<div class="action-panel-actions">
<button class="action-panel-submit"
type="submit"
data-loading-label="Sending..."
data-ga-category="save_share"
data-ga-action="email"
data-ga-label="send">
Send email
</button>
<button class="action-panel-cancel"
aria-label="Close 'Email citations' panel"
ref="linksrc=close_email_panel"
aria-controls="email-action-panel"
aria-expanded="false"
data-ga-category="save_share"
data-ga-action="email"
data-ga-label="cancel">
Cancel
</button>
</div>
<input type="hidden" name="email-search-details" value="" />
<input type="hidden" name="email-search-details-hash" value="0e42663a6c3bd85498fcb88798998fed7bfdc45d457db35281e41afe13cc0524" />
</form>
</div>
</div>
<div id="collections-action-panel"
class="collections-action-panel action-panel in-progress-dots-panel"
aria-hidden="true"
data-collections-open-panel-enabled="false"
data-collections-open-panel-url-hash="#open-collections-panel">
<div class="inner-wrap">
<h3 class="action-panel-heading">
Add to Collections
</h3>
<form id="collections-action-panel-form"
class="collections-action-panel-form action-panel-content action-form action-panel-smaller-selectors"
data-existing-collections-url="/list-existing-collections/"
data-add-to-existing-collection-url="/add-to-existing-collection/"
data-create-and-add-to-new-collection-url="/create-and-add-to-new-collection/"
data-get-article-ids-by-search-url="/get-article-ids-by-search/"
data-myncbi-max-collection-name-length="100"
data-add-to-collection-max-amount="1000"
data-collections-root-url="https://www.ncbi.nlm.nih.gov/myncbi/collections/">
<input type="hidden" name="csrfmiddlewaretoken" value="VjFw3O69yIn5ky1QizwnyTG9jAYYwOxac6pBGEzv8jazeZ7GVS9p21cNREGapp5u">
<div class="choice-group" role="radiogroup">
<ul class="radio-group-items">
<li>
<input type="radio"
id="collections-action-panel-new"
class="collections-new"
name="collections"
value="new"
data-ga-category="save_share"
data-ga-action="collections"
data-ga-label="collections_radio_new">
<label for="collections-action-panel-new">Create a new collection</label>
</li>
<li>
<input type="radio"
id="collections-action-panel-existing"
class="collections-existing"
name="collections"
value="existing"
checked="true"
data-ga-category="save_share"
data-ga-action="collections"
data-ga-label="collections_radio_existing">
<label for="collections-action-panel-existing">Add to an existing collection</label>
</li>
</ul>
</div>
<div class="controls-wrapper">
<div class="action-panel-control-wrap new-collections-controls">
<label for="collections-action-panel-add-to-new" class="action-panel-label required-field-asterisk">
Name your collection:
</label>
<input
type="text"
name="add-to-new-collection"
id="collections-action-panel-add-to-new"
class="collections-action-add-to-new"
pattern="[^&quot;&amp;=&lt;&gt;\/]*" title="The following characters are not allowed in the Name field: &quot;&amp;=&lt;&gt;/"
maxlength="100"
data-ga-category="save_share"
data-ga-action="create_collection"
data-ga-label="non_favorties_collection">
<div class="collections-new-name-too-long usa-input-error-message selection-validation-message">
Name must be less than 100 characters
</div>
</div>
<div class="action-panel-control-wrap existing-collections-controls">
<label for="collections-action-panel-add-to-existing" class="action-panel-label">
Choose a collection:
</label>
<select id="collections-action-panel-add-to-existing"
class="action-panel-selector collections-action-add-to-existing"
data-ga-category="save_share"
data-ga-action="select_collection"
data-ga-label="($('#collections-action-add-to-existing').val() === 'Favorites') ? 'Favorites' : 'non_favorites_collection'">
</select>
<div class="collections-retry-load-on-error usa-input-error-message selection-validation-message">
Unable to load your collection due to an error<br>
<a href="#">Please try again</a>
</div>
</div>
</div>
<div class="action-panel-actions">
<button class="action-panel-submit"
type="submit"
data-loading-label="Adding..."
data-pinger-ignore
data-ga-category="save_share"
data-ga-action="collections"
data-ga-label="add">
Add
</button>
<button class="action-panel-cancel"
aria-label="Close 'Add to Collections' panel"
ref="linksrc=close_collections_panel"
aria-controls="collections-action-panel"
aria-expanded="false"
data-ga-category="save_share"
data-ga-action="collections"
data-ga-label="cancel">
Cancel
</button>
</div>
</form>
</div>
</div>
<div id="bibliography-action-panel"
class="bibliography-action-panel action-panel in-progress-dots-panel"
aria-hidden="true"
data-bibliography-open-panel-enabled="false"
data-bibliography-open-panel-url-hash="#open-bibliography-panel">
<div class="inner-wrap">
<h3 class="action-panel-heading">
Add to My Bibliography
</h3>
<form id="bibliography-action-panel-form"
class="bibliography-action-panel-form action-panel-content action-form action-panel-smaller-selectors"
data-add-to-bibliography-max-amount="100"
data-add-to-bibliography-batch-size="10"
data-bibliography-delegates-url="/list-bibliography-delegates/"
data-add-to-bibliography-url="/add-to-bibliography/"
data-get-article-ids-by-search-url="/get-article-ids-by-search/"
data-mybib-root-url="https://www.ncbi.nlm.nih.gov/myncbi/collections/mybibliography/">
<input type="hidden" name="csrfmiddlewaretoken" value="VjFw3O69yIn5ky1QizwnyTG9jAYYwOxac6pBGEzv8jazeZ7GVS9p21cNREGapp5u">
<div class="action-panel-control-wrap bibliographies-controls">
<div class="choice-group">
<ul class="bibliographies-action-add radio-group-items">
<li>
<input name="bibliography" id="my-bibliography" class="my-bibliography" type="radio" checked/>
<label for="my-bibliography">My Bibliography</label>
</li>
</ul>
</div>
</div>
<div class="bibliographies-retry-load-on-error usa-input-error-message selection-validation-message">
Unable to load your delegates due to an error<br>
<a href="#">Please try again</a>
</div>
<div class="action-panel-actions">
<button class="action-panel-submit"
type="submit"
data-loading-label="Adding..."
data-pinger-ignore>
Add
</button>
<button class="action-panel-cancel"
aria-label="Close 'Add to bibliography' panel"
ref="linksrc=close_bibliography_panel"
aria-controls="bibliography-action-panel"
aria-expanded="false"
data-ga-category="save_share"
data-ga-action="mybib"
data-ga-label="cancel">
Cancel
</button>
</div>
</form>
</div>
</div>
<div id="saved-search-action-panel" class="saved-search-action-panel action-panel " aria-hidden="true"
data-saved-search-open-panel-enabled="false"
data-saved-search-open-panel-url-hash="#open-saved-search-panel">
<div class="inner-wrap">
<h2 class="action-panel-heading">
Your saved search
</h2>
<form id="saved-search-action-panel-form"
class="saved-search-action-panel-form action-panel-content action-form"
data-create-saved-search-url="/create-saved-search/"
data-try-search-terms-url="/try-search-term/"
data-saved-search-root-url="https://www.ncbi.nlm.nih.gov/myncbi/searches/">
<input type="hidden" name="csrfmiddlewaretoken" value="VjFw3O69yIn5ky1QizwnyTG9jAYYwOxac6pBGEzv8jazeZ7GVS9p21cNREGapp5u">
<div class="action-panel-control-wrap">
<label for="saved-search-name" class="action-panel-label saved-search-name-label required-field-asterisk">
Name of saved search:
</label>
<input maxlength="200"
type="text"
name="saved-search-name"
id="saved-search-name"
class="saved-search-name"
value=""
required
pattern="[^&quot;&amp;=&lt;&gt;\/]*" title="The following characters are not allowed in the Name field: &quot;&amp;=&lt;&gt;/">
</div>
<div class="action-panel-control-wrap">
<label for="saved-search-term" class="action-panel-label required-field-asterisk">
Search terms:
</label>
<textarea name="saved-search-term" id="saved-search-term" class="saved-search-term" required></textarea>
</div>
<div class="test-search-term-wrap">
<a href="#" class="try-search-term">Test search terms</a>
</div>
<div class="choice-group action-panel-extra-margin-top">
<span class="action-panel-label" id="fieldset-label">
Would you like email updates of new search results?
</span>
<fieldset id="saved-search-alert" aria-describedby="fieldset-label">
<legend class="usa-sr-only">Saved Search Alert Radio Buttons</legend>
<ul class="radio-group-items">
<li>
<input type="radio" id="saved-search-alert-yes" class="saved-search-alert-yes" name="saved-search-alert" value="yes" checked>
<label for="saved-search-alert-yes" class="action-panel-label">Yes</label>
</li>
<li>
<input aria-label="No radio input" type="radio" id="saved-search-alert-no" class="saved-search-alert-no" name="saved-search-alert" value="no">
<label for="saved-search-alert-no" class="action-panel-label">No</label>
</li>
</ul>
</fieldset>
</div>
<div class="alert-schedule-wrap">
<div class="action-panel-control-wrap">
<label class="action-panel-label">
Email:
</label>
<span aria-label="Email address" id="saved-search-email" class="action-panel-label"><span class="action-panel-label-bold"></span> (<a class="myncbi-account-settings" href="https://www.ncbi.nlm.nih.gov/account/settings/">change</a>)</span>
</div>
<div class="action-panel-control-wrap action-panel-extra-margin-top">
<label for="saved-search-frequency" class="action-panel-label">
Frequency:
</label>
<select id="saved-search-frequency" class="no-border-panel-selector saved-search-frequency">
<option value="monthly">Monthly</option>
<option value="weekly">Weekly</option>
<option value="daily">Daily</option>
</select>
</div>
<div class="action-panel-control-wrap saved-search-monthly-additional">
<label for="saved-search-monthly-on-day" class="action-panel-label">
Which day?
</label>
<select id="saved-search-monthly-on-day" class="no-border-panel-selector">
<option value="Sunday">The first Sunday</option>
<option value="Monday">The first Monday</option>
<option value="Tuesday">The first Tuesday</option>
<option value="Wednesday">The first Wednesday</option>
<option value="Thursday">The first Thursday</option>
<option value="Friday">The first Friday</option>
<option value="Saturday">The first Saturday</option>
<option value="day">The first day</option>
<option value="weekday">The first weekday</option>
</select>
</div>
<div class="action-panel-control-wrap saved-search-weekly-additional">
<label for="saved-search-weekly-on-day" class="action-panel-label">
Which day?
</label>
<select id="saved-search-weekly-on-day" class="no-border-panel-selector saved-search-weekly-on-day">
<option value="Sunday">Sunday</option>
<option value="Monday">Monday</option>
<option value="Tuesday">Tuesday</option>
<option value="Wednesday">Wednesday</option>
<option value="Thursday">Thursday</option>
<option value="Friday">Friday</option>
<option value="Saturday">Saturday</option>
</select>
</div>
<div class="action-panel-control-wrap">
<label for="saved-search-report" class="action-panel-label">
Report format:
</label>
<select id="saved-search-report" class="no-border-panel-selector saved-search-report">
<option value="DocSum">Summary</option>
<option value="DocSumText">Summary (text)</option>
<option value="Abstract">Abstract</option>
<option value="AbstractText">Abstract (text)</option>
<option value="MEDLINE">PubMed</option>
</select>
</div>
<div class="action-panel-control-wrap">
<label for="saved-search-amount" class="action-panel-label">
Send at most:
</label>
<select id="saved-search-amount" class="no-border-panel-selector saved-search-amount">
<option value="1">1 item</option>
<option value="5" selected>5 items</option>
<option value="10">10 items</option>
<option value="20">20 items</option>
<option value="50">50 items</option>
<option value="100">100 items</option>
<option value="200">200 items</option>
</select>
</div>
<div>
<input type="checkbox" id="saved-search-send-if-no-result" class="saved-search-send-if-no-result" name="saved-search-send-if-no-result">
<label for="saved-search-send-if-no-result" class="action-panel-label smaller-checkbox">
Send even when there aren't any new results
</label>
</div>
<div class="action-panel-control-wrap option-text-in-email-wrap">
<label for="saved-search-email-text" class="action-panel-label">
Optional text in email:
</label>
<textarea name="saved-search-email-text"
id="saved-search-email-text"
class="saved-search-email-text"></textarea>
</div>
</div>
<div class="action-panel-actions">
<button class="action-panel-submit"
type="submit"
data-loading-label="Saving..."
data-ga-category="save_share"
data-ga-action="alert"
data-ga-label="save">
Save
</button>
<button class="action-panel-cancel"
aria-label="Close 'Your saved search' panel"
ref="linksrc=close_saved_search_panel"
aria-controls="saved-search-action-panel"
aria-expanded="false"
data-ga-category="save_share"
data-ga-action="alert"
data-ga-label="cancel">
Cancel
</button>
</div>
</form>
</div>
</div>
<div id="citation-manager-action-panel" class="citation-manager-action-panel action-panel" aria-hidden="true">
<div class="inner-wrap">
<h2 class="action-panel-heading">
Create a file for external citation management software
</h2>
<form id="citation-manager-action-panel-form"
class="action-panel-content action-form"
action="/results-export-ids/"
data-by-search-action="/results-export-search-data/"
data-by-ids-action="/results-export-ids/"
method="post"
data-by-search-method="post"
data-by-ids-method="post">
<input type="hidden" name="csrfmiddlewaretoken" value="VjFw3O69yIn5ky1QizwnyTG9jAYYwOxac6pBGEzv8jazeZ7GVS9p21cNREGapp5u">
<input name="results-format" type="hidden" value="pubmed"/>
<div class="action-panel-actions">
<button class="action-panel-submit"
type="submit"
data-loading-label="Sending..."
data-ga-category="save_share"
data-ga-action="citation_manager"
data-ga-label="save">
Create file
</button>
<button class="action-panel-cancel"
aria-label="Close 'Send citations to citation manager' panel"
ref="linksrc=close_citation_manager_panel"
aria-controls="citation-manager-action-panel"
aria-expanded="false"
data-ga-category="save_share"
data-ga-action="citation_manager"
data-ga-label="cancel">
Cancel
</button>
</div>
</form>
</div>
</div>
<div id="rss-action-panel" class="rss-action-panel action-panel " aria-hidden="true">
<div class="inner-wrap">
<h2 class="action-panel-heading">
Your RSS Feed
</h2>
<form id="rss-action-panel-form"
class="rss-action-panel-form action-panel-content action-form"
data-create-rss-feed-url="/create-rss-feed-url/"
data-search-form-term-value="">
<input type="hidden" name="csrfmiddlewaretoken" value="VjFw3O69yIn5ky1QizwnyTG9jAYYwOxac6pBGEzv8jazeZ7GVS9p21cNREGapp5u">
<div class="action-panel-control-wrap">
<label for="rss-name" class="action-panel-label required-field-asterisk">
Name of RSS Feed:
</label>
<input maxlength="200"
placeholder="Name"
type="text"
name="rss-name"
id="rss-name"
class="rss-name"
value=''
required
pattern="[^&quot;&amp;=&lt;&gt;\/]*" title="The following characters are not allowed in the Name field: &quot;&amp;=&lt;&gt;/">
</div>
<div class="rss-limit-wrap">
<div class="action-panel-control-wrap action-panel-extra-margin-top">
<label for="rss-limit" class="action-panel-label">
Number of items displayed:
</label>
<select id="rss-limit" class="no-border-panel-selector rss-limit">
<option value="5">5</option>
<option value="10">10</option>
<option value="15" selected="selected">15</option>
<option value="20">20</option>
<option value="50">50</option>
<option value="100">100</option>
</select>
</div>
</div>
<div class="action-panel-actions">
<button class="action-panel-submit"
type="submit"
data-loading-label="Creating..."
data-ga-category="save_share"
data-ga-action="alert"
data-ga-label="save">
Create RSS
</button>
<button class="action-panel-cancel"
aria-label="Close 'Your RSS' panel"
ref="linksrc=close_rss_panel"
aria-controls="rss-action-panel"
aria-expanded="false"
data-ga-category="save_share"
data-ga-action="alert"
data-ga-label="cancel">
Cancel
</button>
</div>
<div class="action-panel-control-wrap rss-link-copy-wrap">
<label for="rss-link" class="usa-sr-only">RSS Link</label>
<input placeholder="Your RSS Feed Link" type="text" name="rss-link" id="rss-link" class="rss-link" title="RSS Link">
<button
type="button"
disabled
class="rss-link-copy-button disabled"
data-ga-category="save_share"
data-ga-action="rss"
data-ga-label="copy">
Copy
</button>
</div>
</form>
</div>
</div>
</div>
</div>
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<div class="full-text-links">
<div class="full-view">
<h3 class="title">
Full text links
</h3>
<div class="full-text-links-list">
<a class="link-item
dialog-focus"
href="https://journals.asm.org/doi/10.1128/JVI.02262-14?url_ver=Z39.88-2003&amp;rfr_id=ori:rid:crossref.org&amp;rfr_dat=cr_pub 0pubmed"
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rel="noopener"
ref="linksrc=fulltextorjournal_fulltext&amp;is_pmc=True&amp;PrId=3494&amp;itool=Abstract-def&amp;log$=linkouticon&amp;uid=25428864&amp;db=pubmed&amp;nlmid=0113724"
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Free PMC article
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<a href="#" class="full-text-links-button full-text-links-dialog-trigger">
Full text links
</a>
</div>
</div>
<div class="actions-buttons sidebar"><h3 class="title">Actions</h3><div class="inner-wrap"><button class="citation-button citation-dialog-trigger"
aria-label="Open dialog with citation text in different styles"
data-ga-category="save_share"
data-ga-action="cite"
data-ga-label="open"
data-all-citations-url="/25428864/citations/"
data-citation-style="nlm"
data-pubmed-format-link="/25428864/export/"><span class="button-label">Cite</span></button><link type="text/css" href="ncbi-overlay-block/src/overlay-block.css"><div class="collections-button-container" data-article-id="25428864" data-article-db="pubmed"><button class="collections-button collections-dialog-trigger"
aria-label="Save article in MyNCBI collections."
data-ga-category="collections_button"
data-ga-action="click"
data-ga-label="collections_button"
data-collections-open-dialog-enabled="false"
data-collections-open-dialog-url="https://account.ncbi.nlm.nih.gov/?back_url=https%3A%2F%2Fpubmed.ncbi.nlm.nih.gov%2F25428864%2F%23open-collections-dialog"
data-in-collections="false"><span class="button-label">Collections</span></button><div class="overlay" role="dialog"><div id="collections-action-dialog"
class="dialog collections-dialog"
aria-hidden="true"><div class="title">Add to Collections</div><div class="collections-action-panel action-panel"><form id="collections-action-dialog-form"
class="collections-action-panel-form action-panel-content action-form action-panel-smaller-selectors"
data-existing-collections-url="/list-existing-collections/"
data-add-to-existing-collection-url="/add-to-existing-collection/"
data-create-and-add-to-new-collection-url="/create-and-add-to-new-collection/"
data-myncbi-max-collection-name-length="100"
data-collections-root-url="https://www.ncbi.nlm.nih.gov/myncbi/collections/"><input type="hidden" name="csrfmiddlewaretoken" value="VjFw3O69yIn5ky1QizwnyTG9jAYYwOxac6pBGEzv8jazeZ7GVS9p21cNREGapp5u"><div class="choice-group" role="radiogroup"><ul class="radio-group-items"><li><input type="radio"
id="collections-action-dialog-new"
class="collections-new"
name="collections"
value="new"
data-ga-category="collections_button"
data-ga-action="click"
data-ga-label="collections_radio_new"><label for="collections-action-dialog-new">Create a new collection</label></li><li><input type="radio"
id="collections-action-dialog-existing"
class="collections-existing"
name="collections"
value="existing"
checked="true"
data-ga-category="collections_button"
data-ga-action="click"
data-ga-label="collections_radio_existing"><label for="collections-action-dialog-existing">Add to an existing collection</label></li></ul></div><div class="controls-wrapper"><div class="action-panel-control-wrap new-collections-controls"><label for="collections-action-dialog-add-to-new" class="action-panel-label required-field-asterisk">
Name your collection:
</label><input
type="text"
name="add-to-new-collection"
id="collections-action-dialog-add-to-new"
class="collections-action-add-to-new"
pattern="[^&quot;&amp;=&lt;&gt;\/]*" title="The following characters are not allowed in the Name field: &quot;&amp;=&lt;&gt;/"
maxlength="100"
data-ga-category="collections_button"
data-ga-action="create_collection"
data-ga-label="non_favorties_collection"><div class="collections-new-name-too-long usa-input-error-message selection-validation-message">
Name must be less than 100 characters
</div></div><div class="action-panel-control-wrap existing-collections-controls"><label for="collections-action-dialog-add-to-existing" class="action-panel-label">
Choose a collection:
</label><select id="collections-action-dialog-add-to-existing"
class="action-panel-selector collections-action-add-to-existing"
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SAMD9 is an innate antiviral host factor with stress response properties that can be antagonized by poxviruses
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We show that SAMD9 is an innate host antiviral stress response element that participates in the formation of antiviral granules. Poxviruses, myxoma virus and vaccinia virus specifically, utilize a virus-encoded host range factor(s), such as a member of the C7L superfamily, to antagonize SAMD9 to prevent granule formation in a eukaryotic initiation factor 2α (eIF2α)-independent manner. When SAMD9 is stimulated due to failure of the viral antagonism during infection, the resulting antiviral granules exhibit properties different from those of the canonical stress granules.
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<meta itemprop="width" itemtype="http://schema.org/ImageObject" content="800">
<meta itemprop="height" itemtype="http://schema.org/ImageObject" content="952">
<div class="figure-caption figure-caption-text" itemtype="http://schema.org/ImageObject" itemprop="caption" aria-hidden="true">
<div class="caption-wrap">
<strong class="figure-label">
<p> FIG 1 </p>
</strong>
<div class="figure-caption-contents"><p> Infection by MYXV-M062R-null (vMyxM062RKO) leads… </p></div>
</div>
</div>
<div class="figure-caption-medium figure-caption-text" aria-hidden="true">
<strong class="figure-label">
<p> FIG 1 </p>
</strong>
<div class="figure-caption-contents"><p> Infection by MYXV-M062R-null (vMyxM062RKO) leads to the formation of SAMD9 granules. (A) SAMD9… </p></div>
</div>
<figcaption id="figure-caption-0" class="figure-caption-full figure-caption-text" itemtype="http://schema.org/ImageObject" itemprop="description">
<strong class="figure-label">
FIG 1
</strong>
<div class="figure-caption-contents">Infection by MYXV-M062R-null (vMyxM062RKO) leads to the formation of SAMD9 granules. (A) SAMD9 forms a granule structure during vMyxM062RKO infection. HeLa cells were mock treated or infected with wild-type MYXV [vMyxGFP (wt)] or vMyxM062RKO at a multiplicity of infection (MOI) of 10 for 18 h. Cells were fixed with 4% paraformaldehyde and permeabilized with cold methanol before they were incubated with primary antibodies (SAMD9 and G3BP1; Sigma-Aldrich and Santa Cruz Biotechnologies, respectively) and then secondary antibodies (Invitrogen). Samples were mounted for fluorescence microscopy (Nikon C2 confocal microscope). The scale bar represents a length of 100 μm. A total of 91.0% (±6.2% SD) of infected cells (GFP positive and/or viral factory positive) showed SAMD9 antiviral granules; within the viral factories, G3BP1 colocalizes with SAMD9 (the quantification was conducted from three independent experiments and four random views of image with 15 to 31 cells per view in each experiment). (B) SAMD9 granules colocalize with markers of stress granules (SGs). HeLa cells were mock treated or infected with wild-type MYXV or vMyxM062RKO viruses at a MOI of 10 for 18 h before immunofluorescence (IF) staining for SAMD9 (Alexa Fluor 594), G3BP1 (Alexa Fluor 350), and eIF4G (Alexa Fluor 647) was performed as described for panel A. Fluorescent images were captured with a Nikon C2 confocal microscope at 100× magnification. Scale bar, 50 μm.</div>
</figcaption>
</figure>
<figure class="figure-item "
itemscope itemtype="http://schema.org/ImageObject"
itemprop="associatedMedia"
data-slide-index="1"
data-label-slug="fig-2">
<a class="figure-link"
href="https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8d/4300762/ea71117eaa00/zjv999090015002a.jpg"
itemprop="contentUrl"
aria-describedby="figure-caption-1"
role="button"
data-image-width="793"
data-image-height="1412"
data-image-alt="FIG 2"
data-pmc-id="PMC4300762"
data-figure-id="F2">
<img class="figure-thumb" itemprop="thumbnail"
id="article-image-1"
src="https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8d/4300762/695fd2929cf9/zjv999090015002a.gif"
alt="FIG 2" />
</a>
<meta itemprop="width" itemtype="http://schema.org/ImageObject" content="793">
<meta itemprop="height" itemtype="http://schema.org/ImageObject" content="1412">
<div class="figure-caption figure-caption-text" itemtype="http://schema.org/ImageObject" itemprop="caption" aria-hidden="true">
<div class="caption-wrap">
<strong class="figure-label">
<p> FIG 2 </p>
</strong>
<div class="figure-caption-contents"><p> Abortive infection by E3L knockout… </p></div>
</div>
</div>
<div class="figure-caption-medium figure-caption-text" aria-hidden="true">
<strong class="figure-label">
<p> FIG 2 </p>
</strong>
<div class="figure-caption-contents"><p> Abortive infection by E3L knockout VACV (VACV-E3LKO- <sub> L </sub> tdTr) or C7LK1L double-knockout VACV… </p></div>
</div>
<figcaption id="figure-caption-1" class="figure-caption-full figure-caption-text" itemtype="http://schema.org/ImageObject" itemprop="description">
<strong class="figure-label">
FIG 2
</strong>
<div class="figure-caption-contents">Abortive infection by E3L knockout VACV (VACV-E3LKO-<sub>L</sub>tdTr) or C7LK1L double-knockout VACV (VACV-C7LK1L-DKO) stimulates SAMD9 granule formation. (A) SAMD9 antiviral granules form after VACV-E3LKO-<sub>L</sub>tdTr (92.1% ± 8.4% SD) or VACV-C7LK1L-DKO (91.8% ± 8.3% SD) infection; meanwhile, G3BP1 colocalizes with SAMD9 in the viral factories. Wild-type or knockout VACV infection was conducted at a MOI of 5 for 5 h p.i. on HeLa cells before cells were fixed and permeabilized for IF staining of SAMD9 (Alexa Fluor 594) and G3BP1 (Alexa Fluor 647). Nuclei and viral factories were stained with DAPI (4,6-diamidino-2-phenylindole). Low-level of tdTr expression driven by the late poxvirus promoter is not detectable at this time of the infection, and thus it does not interfere with the observation of Alexa Fluor 594. Fluorescent images were captured with a Nikon C2 confocal microscope. Quantification was conducted from the results of up to five independent experiments. The arrows point to an uninfected cell in the VACV-C7LK1L-DKO infection. Scale bar, 50 μm. (B) Double-stranded RNA can be detected within the SAMD9 granules. Infection by MYXV and VACV was conducted at 19 and 5 h p.i., respectively. After fixing and permeabilization, cells were probed with SAMD9, dsRNA (English and Scientific Consulting Kft.), and DAPI for IF. Fluorescence microscopic observation was performed as described for panel A. Scale bar, 50 μm. (C) The formation of SAMD9 antiviral granules by poxvirus infection is eIF2α phosphorylation independent. HeLa cells were infected with VACV (lane 3, VACV-<sub>E/L</sub>GFP/<sub>L</sub>tdTr; lane 4, VACV-K1LKO-<sub>L</sub>tdTr; lane 5, VACV-C7LK1L-DKO; lane 6, VACV-E3LKO-<sub>L</sub>tdTr) for 5 h at a MOI of 5 or with MYXV (lane 7, vMyxM062RKO; lane 8, vMyxGFP) for 19 h before they were harvested for Western blotting. As controls, cells were either mock treated (lane 1) or treated with sodium arsenate (SA) (1 mM) for 1 h (lane 2). Total proteins of 20 μg were separated using 12% SDS-PAGE before they were transferred to a polyvinylidene difluoride (PVDF) membrane for probing with phosphorylated eIF2α (Cell Signaling) and later with total eIF2α (Cell Signaling).</div>
</figcaption>
</figure>
<figure class="figure-item "
itemscope itemtype="http://schema.org/ImageObject"
itemprop="associatedMedia"
data-slide-index="2"
data-label-slug="fig-2">
<a class="figure-link"
href="https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8d/4300762/d7575afea0a4/zjv999090015002b.jpg"
itemprop="contentUrl"
aria-describedby="figure-caption-2"
role="button"
data-image-width="679"
data-image-height="261"
data-image-alt="FIG 2"
data-pmc-id="PMC4300762"
data-figure-id="F2">
<img class="figure-thumb" itemprop="thumbnail"
id="article-image-2"
src="https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8d/4300762/695fd2929cf9/zjv999090015002a.gif"
alt="FIG 2" />
</a>
<meta itemprop="width" itemtype="http://schema.org/ImageObject" content="679">
<meta itemprop="height" itemtype="http://schema.org/ImageObject" content="261">
<div class="figure-caption figure-caption-text" itemtype="http://schema.org/ImageObject" itemprop="caption" aria-hidden="true">
<div class="caption-wrap">
<strong class="figure-label">
<p> FIG 2 </p>
</strong>
<div class="figure-caption-contents"><p> Abortive infection by E3L knockout… </p></div>
</div>
</div>
<div class="figure-caption-medium figure-caption-text" aria-hidden="true">
<strong class="figure-label">
<p> FIG 2 </p>
</strong>
<div class="figure-caption-contents"><p> Abortive infection by E3L knockout VACV (VACV-E3LKO- <sub> L </sub> tdTr) or C7LK1L double-knockout VACV… </p></div>
</div>
<figcaption id="figure-caption-2" class="figure-caption-full figure-caption-text" itemtype="http://schema.org/ImageObject" itemprop="description">
<strong class="figure-label">
FIG 2
</strong>
<div class="figure-caption-contents">Abortive infection by E3L knockout VACV (VACV-E3LKO-<sub>L</sub>tdTr) or C7LK1L double-knockout VACV (VACV-C7LK1L-DKO) stimulates SAMD9 granule formation. (A) SAMD9 antiviral granules form after VACV-E3LKO-<sub>L</sub>tdTr (92.1% ± 8.4% SD) or VACV-C7LK1L-DKO (91.8% ± 8.3% SD) infection; meanwhile, G3BP1 colocalizes with SAMD9 in the viral factories. Wild-type or knockout VACV infection was conducted at a MOI of 5 for 5 h p.i. on HeLa cells before cells were fixed and permeabilized for IF staining of SAMD9 (Alexa Fluor 594) and G3BP1 (Alexa Fluor 647). Nuclei and viral factories were stained with DAPI (4,6-diamidino-2-phenylindole). Low-level of tdTr expression driven by the late poxvirus promoter is not detectable at this time of the infection, and thus it does not interfere with the observation of Alexa Fluor 594. Fluorescent images were captured with a Nikon C2 confocal microscope. Quantification was conducted from the results of up to five independent experiments. The arrows point to an uninfected cell in the VACV-C7LK1L-DKO infection. Scale bar, 50 μm. (B) Double-stranded RNA can be detected within the SAMD9 granules. Infection by MYXV and VACV was conducted at 19 and 5 h p.i., respectively. After fixing and permeabilization, cells were probed with SAMD9, dsRNA (English and Scientific Consulting Kft.), and DAPI for IF. Fluorescence microscopic observation was performed as described for panel A. Scale bar, 50 μm. (C) The formation of SAMD9 antiviral granules by poxvirus infection is eIF2α phosphorylation independent. HeLa cells were infected with VACV (lane 3, VACV-<sub>E/L</sub>GFP/<sub>L</sub>tdTr; lane 4, VACV-K1LKO-<sub>L</sub>tdTr; lane 5, VACV-C7LK1L-DKO; lane 6, VACV-E3LKO-<sub>L</sub>tdTr) for 5 h at a MOI of 5 or with MYXV (lane 7, vMyxM062RKO; lane 8, vMyxGFP) for 19 h before they were harvested for Western blotting. As controls, cells were either mock treated (lane 1) or treated with sodium arsenate (SA) (1 mM) for 1 h (lane 2). Total proteins of 20 μg were separated using 12% SDS-PAGE before they were transferred to a polyvinylidene difluoride (PVDF) membrane for probing with phosphorylated eIF2α (Cell Signaling) and later with total eIF2α (Cell Signaling).</div>
</figcaption>
</figure>
<figure class="figure-item "
itemscope itemtype="http://schema.org/ImageObject"
itemprop="associatedMedia"
data-slide-index="3"
data-label-slug="fig-3">
<a class="figure-link"
href="https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8d/4300762/d4226bfd3471/zjv9990900150003.jpg"
itemprop="contentUrl"
aria-describedby="figure-caption-3"
role="button"
data-image-width="750"
data-image-height="501"
data-image-alt="FIG 3"
data-pmc-id="PMC4300762"
data-figure-id="F3">
<img class="figure-thumb" itemprop="thumbnail"
id="article-image-3"
src="https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8d/4300762/0c969993313d/zjv9990900150003.gif"
alt="FIG 3" />
</a>
<meta itemprop="width" itemtype="http://schema.org/ImageObject" content="750">
<meta itemprop="height" itemtype="http://schema.org/ImageObject" content="501">
<div class="figure-caption figure-caption-text" itemtype="http://schema.org/ImageObject" itemprop="caption" aria-hidden="true">
<div class="caption-wrap">
<strong class="figure-label">
<p> FIG 3 </p>
</strong>
<div class="figure-caption-contents"><p> SAMD9 is a stress-responding element… </p></div>
</div>
</div>
<div class="figure-caption-medium figure-caption-text" aria-hidden="true">
<strong class="figure-label">
<p> FIG 3 </p>
</strong>
<div class="figure-caption-contents"><p> SAMD9 is a stress-responding element that participates in stress granule formation. HeLa cells… </p></div>
</div>
<figcaption id="figure-caption-3" class="figure-caption-full figure-caption-text" itemtype="http://schema.org/ImageObject" itemprop="description">
<strong class="figure-label">
FIG 3
</strong>
<div class="figure-caption-contents">SAMD9 is a stress-responding element that participates in stress granule formation. HeLa cells are treated with sodium arsenate (SA) (1 mM) or DMDA-Pat A (1 μM) for 1 h before IF staining of SAMD9, G3BP1, and nuclei as described for Fig. 1 and 2. mk, mock treatment.</div>
</figcaption>
</figure>
<figure class="figure-item "
itemscope itemtype="http://schema.org/ImageObject"
itemprop="associatedMedia"
data-slide-index="4"
data-label-slug="fig-4">
<a class="figure-link"
href="https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8d/4300762/87ec6f4fbe7f/zjv999090015004a.jpg"
itemprop="contentUrl"
aria-describedby="figure-caption-4"
role="button"
data-image-width="745"
data-image-height="927"
data-image-alt="FIG 4"
data-pmc-id="PMC4300762"
data-figure-id="F4">
<img class="figure-thumb" itemprop="thumbnail"
id="article-image-4"
src="https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8d/4300762/66b031b85b15/zjv999090015004a.gif"
alt="FIG 4" />
</a>
<meta itemprop="width" itemtype="http://schema.org/ImageObject" content="745">
<meta itemprop="height" itemtype="http://schema.org/ImageObject" content="927">
<div class="figure-caption figure-caption-text" itemtype="http://schema.org/ImageObject" itemprop="caption" aria-hidden="true">
<div class="caption-wrap">
<strong class="figure-label">
<p> FIG 4 </p>
</strong>
<div class="figure-caption-contents"><p> Knocking down SAMD9 rescues MYXV-M062R-null… </p></div>
</div>
</div>
<div class="figure-caption-medium figure-caption-text" aria-hidden="true">
<strong class="figure-label">
<p> FIG 4 </p>
</strong>
<div class="figure-caption-contents"><p> Knocking down SAMD9 rescues MYXV-M062R-null (vMyxM062RKO) and C7LK1L double-knockout VACV (VACV-C7LK1L-DKO) by disengaging… </p></div>
</div>
<figcaption id="figure-caption-4" class="figure-caption-full figure-caption-text" itemtype="http://schema.org/ImageObject" itemprop="description">
<strong class="figure-label">
FIG 4
</strong>
<div class="figure-caption-contents">Knocking down SAMD9 rescues MYXV-M062R-null (vMyxM062RKO) and C7LK1L double-knockout VACV (VACV-C7LK1L-DKO) by disengaging the antiviral granule formation. (A) SAMD9 is responsible for the antiviral granule formation stimulated by either vMyxM062RKO (a) or VACV-C7LK1L-DKO (b) but not for the antiviral granule formation stimulated by E3L-knockout VACV (VACV-E3LKO-<sub>L</sub>tdTr) (c). Antiviral granule formation was investigated at 19 h p.i. for vMyxM062RKO and at 5 h p.i. for VACV infection of normal HeLa cells or SAMD9 knockdown (SAMD9KD) at a MOI of 10 and a MOI of 5, respectively. After IF staining of SAMD9, G3BP1, and nuclei, images were captured with a Nikon c2 confocal microscope. Scale bar, 50 μm. (B) Knocking down SAMD9 expression rescues M062R-null MYXV replication. HeLa cells stably expressing shRNAs targeting SAMD9 (SAMD9KD) showed significantly reduced SAMD9 protein levels compared with control HeLa cells (con). A total protein of 40 μg was separated on SDS-PAGE for Western blotting against SAMD9 and β-actin. Multiple-step growth curve analysis of MYXV-M062R-null was conducted on control HeLa (con) or SAMD9 knockdown (SAMD9KD) HeLa cells. Duplicate of infection at each time point per virus was conducted. Titration was performed on BSC40 cells in triplicate at each dilution. The growth curve shown is one view representative of the results of two independent experiments. ffu, focus-forming units. (C) Knocking down SAMD9 expression rescues viral replication of VACV-C7LK1L-DKO. A549 cells stably expressing control shRNA (A549-con) or shRNAs targeting SAMD9 (A549-SAMD9KD) were engineered by infecting cells with lentivirus containing corresponding shRNAs. Western blot analysis was conducted with a total protein of 40 μg from either A549-con or A549-SAMD9KD by probing against SAMD9 and β-actin. The experiment designed to construct the multiple-step growth curve of VACV-C7LK1L-DKO was performed by infecting control or knockdown cells at a low MOI of 0.1 followed by harvesting at different time points. At each time point, samples from triplicate infections were collected for titration on BSC40 cells. The growth curve shown is a view representative of the results of two independent experiments.</div>
</figcaption>
</figure>
<figure class="figure-item "
itemscope itemtype="http://schema.org/ImageObject"
itemprop="associatedMedia"
data-slide-index="5"
data-label-slug="fig-4">
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href="https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8d/4300762/1060f43343a3/zjv999090015004b.jpg"
itemprop="contentUrl"
aria-describedby="figure-caption-5"
role="button"
data-image-width="749"
data-image-height="1568"
data-image-alt="FIG 4"
data-pmc-id="PMC4300762"
data-figure-id="F4">
<img class="figure-thumb" itemprop="thumbnail"
id="article-image-5"
src="https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5b8d/4300762/66b031b85b15/zjv999090015004a.gif"
alt="FIG 4" />
</a>
<meta itemprop="width" itemtype="http://schema.org/ImageObject" content="749">
<meta itemprop="height" itemtype="http://schema.org/ImageObject" content="1568">
<div class="figure-caption figure-caption-text" itemtype="http://schema.org/ImageObject" itemprop="caption" aria-hidden="true">
<div class="caption-wrap">
<strong class="figure-label">
<p> FIG 4 </p>
</strong>
<div class="figure-caption-contents"><p> Knocking down SAMD9 rescues MYXV-M062R-null… </p></div>
</div>
</div>
<div class="figure-caption-medium figure-caption-text" aria-hidden="true">
<strong class="figure-label">
<p> FIG 4 </p>
</strong>
<div class="figure-caption-contents"><p> Knocking down SAMD9 rescues MYXV-M062R-null (vMyxM062RKO) and C7LK1L double-knockout VACV (VACV-C7LK1L-DKO) by disengaging… </p></div>
</div>
<figcaption id="figure-caption-5" class="figure-caption-full figure-caption-text" itemtype="http://schema.org/ImageObject" itemprop="description">
<strong class="figure-label">
FIG 4
</strong>
<div class="figure-caption-contents">Knocking down SAMD9 rescues MYXV-M062R-null (vMyxM062RKO) and C7LK1L double-knockout VACV (VACV-C7LK1L-DKO) by disengaging the antiviral granule formation. (A) SAMD9 is responsible for the antiviral granule formation stimulated by either vMyxM062RKO (a) or VACV-C7LK1L-DKO (b) but not for the antiviral granule formation stimulated by E3L-knockout VACV (VACV-E3LKO-<sub>L</sub>tdTr) (c). Antiviral granule formation was investigated at 19 h p.i. for vMyxM062RKO and at 5 h p.i. for VACV infection of normal HeLa cells or SAMD9 knockdown (SAMD9KD) at a MOI of 10 and a MOI of 5, respectively. After IF staining of SAMD9, G3BP1, and nuclei, images were captured with a Nikon c2 confocal microscope. Scale bar, 50 μm. (B) Knocking down SAMD9 expression rescues M062R-null MYXV replication. HeLa cells stably expressing shRNAs targeting SAMD9 (SAMD9KD) showed significantly reduced SAMD9 protein levels compared with control HeLa cells (con). A total protein of 40 μg was separated on SDS-PAGE for Western blotting against SAMD9 and β-actin. Multiple-step growth curve analysis of MYXV-M062R-null was conducted on control HeLa (con) or SAMD9 knockdown (SAMD9KD) HeLa cells. Duplicate of infection at each time point per virus was conducted. Titration was performed on BSC40 cells in triplicate at each dilution. The growth curve shown is one view representative of the results of two independent experiments. ffu, focus-forming units. (C) Knocking down SAMD9 expression rescues viral replication of VACV-C7LK1L-DKO. A549 cells stably expressing control shRNA (A549-con) or shRNAs targeting SAMD9 (A549-SAMD9KD) were engineered by infecting cells with lentivirus containing corresponding shRNAs. Western blot analysis was conducted with a total protein of 40 μg from either A549-con or A549-SAMD9KD by probing against SAMD9 and β-actin. The experiment designed to construct the multiple-step growth curve of VACV-C7LK1L-DKO was performed by infecting control or knockdown cells at a low MOI of 0.1 followed by harvesting at different time points. At each time point, samples from triplicate infections were collected for titration on BSC40 cells. The growth curve shown is a view representative of the results of two independent experiments.</div>
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<div id="substances" class="substances keywords-section">
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Substances
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<div id="related-links" class="related-links">
<h2 class="title">
Related information
</h2>
<ul class="related-links-list"><li><a title="PubMed links associated with Books" href="https://www.ncbi.nlm.nih.gov/books?linkname=pubmed_books_refs&amp;from_uid=25428864"
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Cited in Books
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ref="log$=recordlinks&logdbfrom=pubmed&ncbi_uid=25428864&ordinalpos=1&linkpos=2">
Gene
</a></li><li><a title="Link to Gene for the GeneRIF subcategory" href="https://www.ncbi.nlm.nih.gov/gene?linkname=pubmed_gene_rif&amp;from_uid=25428864"
ref="log$=recordlinks&logdbfrom=pubmed&ncbi_uid=25428864&ordinalpos=1&linkpos=3">
Gene (GeneRIF)
</a></li><li><a title="Related records in MedGen based on citations in GeneReviews and Medical Genetics Summaries" href="https://www.ncbi.nlm.nih.gov/medgen?linkname=pubmed_medgen_bookshelf_cited&amp;from_uid=25428864"
ref="log$=recordlinks&logdbfrom=pubmed&ncbi_uid=25428864&ordinalpos=1&linkpos=4">
MedGen (Bookshelf cited)
</a></li><li><a title="Published protein sequences" href="https://www.ncbi.nlm.nih.gov/protein?linkname=pubmed_protein&amp;from_uid=25428864"
ref="log$=recordlinks&logdbfrom=pubmed&ncbi_uid=25428864&ordinalpos=1&linkpos=5">
Protein
</a></li><li><a title="Link to Protein RefSeqs" href="https://www.ncbi.nlm.nih.gov/protein?linkname=pubmed_protein_refseq&amp;from_uid=25428864"
ref="log$=recordlinks&logdbfrom=pubmed&ncbi_uid=25428864&ordinalpos=1&linkpos=6">
Protein (RefSeq)
</a></li></ul>
</div>
<div id="grants" class="grants">
<h2 class="title">
Grants and funding
</h2>
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<div id="linkout" class="linkout">
<h2 class="title">
LinkOut - more resources
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