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<input type="email" aria-label="Sender Email Address" placeholder="email@example.com" id="email-from" class="email-from" pattern="^[a-zA-Z0-9_.+-]+@[a-zA-Z0-9-]+\.[a-zA-Z0-9-.]+$" maxlength="256">
</div>
<div class="action-panel-control-wrap">
<label for="email-citation-format" class="action-panel-label">
Format:
</label>
<select id="email-citation-format" name="citation-format" class="action-panel-selector email-citation-format">
<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="yS8WY1J7X9RmKeg8inNLpNeaFFbuTAwPPFS1BRctxKEQEFmYVGqNTVKOdJTGMb49">
<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="yS8WY1J7X9RmKeg8inNLpNeaFFbuTAwPPFS1BRctxKEQEFmYVGqNTVKOdJTGMb49">
<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="yS8WY1J7X9RmKeg8inNLpNeaFFbuTAwPPFS1BRctxKEQEFmYVGqNTVKOdJTGMb49">
<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="yS8WY1J7X9RmKeg8inNLpNeaFFbuTAwPPFS1BRctxKEQEFmYVGqNTVKOdJTGMb49">
<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="yS8WY1J7X9RmKeg8inNLpNeaFFbuTAwPPFS1BRctxKEQEFmYVGqNTVKOdJTGMb49">
<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>
<div class="article-page" id="article-page" data-article-pmid="39509507">
<aside class="page-sidebar">
<div class="inner-wrap">
<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:///www.science.org/doi/10.1126/science.adp7201?url_ver=Z39.88-2003&amp;rfr_id=ori:rid:crossref.org&amp;rfr_dat=cr_pub 0pubmed"
target="_blank"
rel="noopener"
ref="linksrc=fulltextorjournal_fulltext&amp;is_pmc=False&amp;PrId=4487&amp;itool=Abstract-def&amp;log$=linkouticon&amp;uid=39509507&amp;db=pubmed&amp;nlmid=0404511"
title="See full text options at Atypon"
data-ga-category="full_text"
data-ga-action="Atypon"
data-ga-label="39509507"
><img src="https://cdn.ncbi.nlm.nih.gov/corehtml/query/egifs/https:--www.science.org-pb-assets-images-logos-pubmed-science.gif" alt="Atypon full text link"><span class="text">
Atypon
</span></a><a class="link-item
pmc
"
href="https://pmc.ncbi.nlm.nih.gov/articles/pmid/39509507/"
target="_blank"
rel="noopener"
ref="linksrc=fulltextorjournal_fulltext&amp;is_pmc=True&amp;PrId=3494&amp;itool=Abstract-def&amp;log$=linkouticon&amp;uid=39509507&amp;db=pubmed&amp;nlmid=0404511"
title="Free full text at PubMed Central"
data-ga-category="full_text"
data-ga-action="PMC"
data-ga-label="39509507"
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Free PMC article
</span></a>
</div>
</div>
<div class="short-view">
<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="/39509507/citations/"
data-citation-style="nlm"
data-pubmed-format-link="/39509507/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="39509507" 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%2F39509507%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="yS8WY1J7X9RmKeg8inNLpNeaFFbuTAwPPFS1BRctxKEQEFmYVGqNTVKOdJTGMb49"><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"
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<h1 class="heading-title">
Regulated N-glycosylation controls chaperone function and receptor trafficking
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doi: 10.1126/science.adp7201.
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One-fifth of human proteins are N-glycosylated in the endoplasmic reticulum (ER) by two oligosaccharyltransferases, OST-A and OST-B. Contrary to the prevailing view of N-glycosylation as a housekeeping function, we identified an ER pathway that modulates the activity of OST-A. Genetic analyses linked OST-A to HSP90B1, an ER chaperone for membrane receptors, and CCDC134, an ER luminal protein. During its translocation into the ER, an N-terminal peptide in HSP90B1 templates the assembly of a translocon complex containing CCDC134 and OST-A that protects HSP90B1 during folding, preventing its hyperglycosylation and degradation. Disruption of this pathway impairs WNT and IGF1R signaling and causes the bone developmental disorder osteogenesis imperfecta. Thus, N-glycosylation can be regulated by specificity factors in the ER to control cell surface receptor signaling and tissue development.
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<p xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:p1="http://pubmed.gov/pub-one">The authors declare no competing interests.</p>
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<p> Figure 1. Regulation of HSP90B1 N-glycosylation and… </p>
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<p> Figure 1. Regulation of HSP90B1 N-glycosylation and WNT signaling by an ER protein network. </p>
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<div class="figure-caption-contents"><b> (A)… </b></div>
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<figcaption id="figure-caption-0" class="figure-caption-full figure-caption-text" itemtype="http://schema.org/ImageObject" itemprop="description">
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Figure 1. Regulation of HSP90B1 N-glycosylation and WNT signaling by an ER protein network.
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<div class="figure-caption-contents"><b>(A)</b> DepMap co-essentiality relationships between CCDC134, STT3A, HSP90B1, and OSTC visualized using <i>Fireworks</i> (16). The bi-directional edges between these four genes (bold orange lines) indicate concordant effects on cell growth across &gt;1000 cell lines. <b>(B)</b> Abundances and glycosylation status of HSP90B1, its client LRP6, and PSAP (an exclusive OST-A substrate) in lysates from cells expressing a control (NTC) sgRNA or sgRNAs against the indicated genes. <b>(C)</b> HSP90B1 protein abundance in wild-type (WT), <i>CCDC134</i><sup><i>-/-</i></sup>, <i>STT3A</i><sup><i>-/-</i></sup>, and <i>HSP90B1</i><sup><i>-/-</i></sup> RKO cell lines measured by mass spectrometry, normalized to WT cells. Bars represent the mean abundance +/- SEM from six independent mass spectrometry runs, represented as individual data points. Statistical significance was determined by one-way ANOVA with Dunnetts multiple comparisons test; **** p&lt;0.0001. <b>(D)</b> Domain architecture of HSP90B1. The constitutive and facultative N-glycosylation sites are labeled in green and purple, respectively. The point mutations used to disrupt the one constitutive sequon (1N mutant) and the five facultative sequons (5N mutant) are listed. fig.S2A shows these features on the HSP90B1 three dimensional structure using the same coloring scheme. <b>(E, F)</b> Abundances of glycosylated peptides in <i>CCDC134</i><sup><i>-/-</i></sup> and <i>STT3A</i><sup><i>-/-</i></sup> cells measured using global, unbiased N-glycoprotemics. Each data point represents the fold change in abundance of a distinct glycopeptide (defined by sequence and glycan structure) in mutant compared to wild-type cells. Glycopeptides that include the constitutive and facultative sequons in HSP90B1 are colored green and purple, respectively. Full dataset in Data S2. <b>(G)</b> Enrichment of glycopeptides (normalized to total HSP90B1 protein abundance) that include each of the facultative and constitutive sequons of HSP90B1 in <i>CCDC134</i><sup><i>-/-</i></sup> or <i>STT3A</i><sup><i>-/-</i></sup> cells compared to WT cells. Bars show the mean +/- SEM from six independent mass spectrometry runs, represented as individual data points. The abundances of all peptides that include each HSP90B1 sequon were integrated using individual peptide data summarized in <b>1E and 1F</b> and provided in Data S2. <b>(H, I)</b> Abundance and glycosylation status of HSP90B1 in lysates from three (C1-C3) independent control (NTC) and <i>CCDC134</i><sup><i>-/-</i></sup> clonal cell lines (<b>H</b>), or after the stable expression of HA-tagged CCDC134 in <i>CCDC134</i><sup><i>-/-</i></sup> cells (<b>I</b>). The hyperglycosylated form of HSP90B1 is denoted by a red arrowhead in this and all subsequent panels. <b>(J)</b> LRP6 and LRP5 abundances in total lysate or at the plasma membrane from three independently derived (C1-C3) control (NTC) or <i>CCDC134</i><sup><i>-/-</i></sup> clonal cell lines. The cell surface protein Na/K ATPase and cytoplasmic protein α-tubulin serve as controls, both for loading and for the specificity of cell surface biotinylation. <b>(K)</b> Glycosidase sensitivity in conjunction with mobility on SDS-PAGE gels was used to measure the ER or cell-surface pools of LRP6 in control or <i>CCDC134</i><sup><i>-/-</i></sup> cells. Endoglycosidase H (Endo H) can remove glycans added in the ER but not the complex glycan modifications added in the Golgi; Peptide-<i>N</i>-Glycosidase F (PNGase F) can remove glycans on both ER and cell-surface proteins. <b>(L)</b> Active (non-phosphorylated) β-catenin abundance (a metric of WNT signaling strength) was measured (+/- WNT3A) using immunoblots in wild-type cells or clonal cell lines expressing a control (NTC) sgRNA or an sgRNA targeting <i>CCDC134</i>.</div>
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<p> Figure 2. Hyperglycosylation of HSP90B1 regulates WNT… </p>
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<p> Figure 2. Hyperglycosylation of HSP90B1 regulates WNT signaling strength. </p>
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<div class="figure-caption-contents"><b> (A-D) </b> Abundances of cell-surface LRP6 (…</div>
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Figure 2. Hyperglycosylation of HSP90B1 regulates WNT signaling strength.
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<div class="figure-caption-contents"><b>(A-D)</b> Abundances of cell-surface LRP6 (<b>A</b>,<b>C</b>) or active β-catenin abundance (<b>B</b>,<b>D</b>) in clonally derived cell lines of the indicated genotypes stably expressing wild-type (WT) FLAG-HSP90B1 or variants carrying mutations in the one constitutive (1N) or all five facultative (5N) sites (see Fig.1D). HSP90B1 variants were expressed at comparable levels (fig.S5A). <b>(E)</b> N-glycosylation status of HSP90B1 in <i>STT3B</i><sup><i>-/-</i></sup> and <i>STT3A</i><sup><i>-/-</i></sup> cells expressing different levels of CCDC134: No CCDC134 (<b>-</b>), endogenous CCDC134(<b>+</b>), stably overexpressed 3xHA-CCDC134 (<b>+++</b>) on top of endogenous CCDC134. <b>(F)</b> A provisional pathway diagram constructed based on genetic interactions (dotted lines) uncovered in our work and physical interactions (solid lines) described in the literature.</div>
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<p> Figure 3. The pre-N segment of HSP90B1… </p>
</strong>
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<p> Figure 3. The pre-N segment of HSP90B1 inhibits its own N-glycosylation by recruiting CCDC134 to… </p>
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Figure 3. The pre-N segment of HSP90B1 inhibits its own N-glycosylation by recruiting CCDC134 to an OST-A containing secretory translocon.
</strong>
<div class="figure-caption-contents"><b>(A)</b> Variants of HSP90B1 used for cell-based and <i>in vitro</i> assays. Key features include the ERss, ER signal sequence; FLAG, 3xFLAG tag; pre-N, unstructured segment; NTD, N-terminal domain; MD, middle domain; CTD, C-terminal domain. N-glycosylation sites in pre-N and NTD were eliminated to allow easy assessment of the glycan modification of the three sequons in the M domain by gel shifts (see <b>3B</b> and text). <b>(B)</b> Glycosylation status of HSP90B1 variants shown in <b>3A</b> was assessed using gel shifts and Endo H sensitivity after transient co-expression in HEK293T cells with WT CCDC134 (<b>+</b>) or a non-functional variant (<b>-</b>) lacking its ER signal sequence (see Fig.S3J). The four predicted N-glycoforms (carrying 0, 1, 2 or 3 glycans) are labeled 0N-3N in red lettering. <b>(C)</b> Glycosylation status of the 1-93M variant (see <b>3A</b>) of HSP90B1 carrying the indicated mutations in the “SRT” pseudosubstrate motif found in the pre-N segment. Each construct was co-expressed with functional (<b>+</b>) or non-functional (<b>-</b>) CCDC134. See fig.S6C and S6D for deletion analysis and alanine scanning mutagenesis of the pre-N segment. <b>(D</b>,<b>E)</b> Glycosylation status of chimeric proteins (<b>3D</b>) constructed by fusing variants of the 1-93 segment of HSP90B1 to the obligate OST-A substrate PSAP, which contains five N-glycosylation sites shown in <b>3D</b>. T44A changes “SRT” to “SRA” and A8 changes “RTD” to “AAA” (see <b>3C</b> and fig.S6D). All chimeras carry the ERss of HSP90B1. <b>(F)</b> Constructs used for <i>in vitro</i> translation experiments. To stably stall translation, the STOP codon was removed and a MLKV peptide sequence appended at the C-terminus. <b>(G)</b> Glycosylation status of the 1-93M variant of HSP90B1 (see <b>3A</b>) translated in rabbit reticulocyte lysate (RRL) in the presence of rough microsomal membranes generated from wild-type or clonally-derived <i>CCDC134</i><sup><i>-/-</i></sup>, <i>STT3A</i><sup><i>-/-</i></sup>, or <i>STT3B</i><sup><i>-/-</i></sup> HEK293T cells and concentrated by immunoprecipitation on anti-FLAG beads. The four N-glycoforms of 1-93M are labeled (compare to <b>3B</b>) and show sensitivity to Endo H treatment. <b>(H)</b> Association of endogenous CCDC134 with stalled 1-93M, M domain alone or a 1-93M variant carrying a T44A mutation in the “SRT” pseudosubstrate site (see <b>3C</b>). The stalled nascent chain, immunoprecipitated (IP) using anti-FLAG beads, associates with the ribosome (RPL17) and known components of the secretory translocon (STT3A, the SEC61 channel, and the TRAP complex), but not with components of the multi-pass translocon (NOMO2) or the ER-Membrane Protein Complex (EMC3) (34, 41). NC-tRNA: nascent chain-tRNA conjugates.</div>
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<p> Figure 4. The oligosaccharyltransferase activity of OST-A… </p>
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<p> Figure 4. The oligosaccharyltransferase activity of OST-A is not required to promote HSP90B1 stability and… </p>
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Figure 4. The oligosaccharyltransferase activity of OST-A is not required to promote HSP90B1 stability and WNT signaling.
</strong>
<div class="figure-caption-contents"><b>(A</b>,<b>B)</b> Glycosylation status and abundances of PSAP (<b>A</b>), active β-catenin (<b>A</b>), CCDC134 (<b>A</b>), HSP90B1 <b>(B)</b> and cell-surface LRP6 (<b>B</b>) in wild-type (WT) cells or <i>STT3A</i><sup><i>-/-</i></sup> cells stably expressing FLAG-STT3A variants carrying mutations in various sites involved in catalytic transfer of the glycan from the lipid-linked oligosaccharide to the asparagine in sequons. Variants (shown on a structure in fig.S9A) carry mutations in residues involved in active site chemistry (AS), lipid-linked oligosaccharide binding (LLO), sequon binding (WWD) or N-glycosylation of STT3A itself (N and NN). Glycosylation of PSAP (<b>A</b>) was used to assess OST-A activity in cells. See fig.S9B. <b>(C)</b> HSP90B1 protein abundance in wild-type (WT) cells, <i>STT3A</i><sup><i>-/-</i></sup> cells, and <i>STT3A</i><sup><i>-/-</i></sup> cells stably expressing wild-type or catalytically inactive (AS) STT3A. The STT3A-AS variant carries mutations in four residues involved in the chemical step of glycan transfer (fig.S9A). Statistical significance was determined by one-way ANOVA with Dunnetts multiple comparisons test; **** p&lt;0.0001. <b>(D)</b> Abundance and glycosylation status (red arrowhead) of endogenous HSP90B1 in <i>STT3A</i><sup><i>-/-</i></sup> cells stably expressing (1) catalytically inactive FLAG-STT3A-AS carrying mutations in active site residues (fig.S9A) and (2) sgRNAs targeting CCDC134 or OSTC. sgNTC=non-targeting control sgRNA. <b>(E)</b> During translation, HSP90B1 is tethered to a specialized CCDC134-containing translocon that forms a specialized microenvironment for its folding. Tethering interactions are shown in the circular inset: CCDC134 interacts both with STT3A and HSP90B1, while the pre-N domain of HSP90B1 itself binds to the sequon binding site of STT3A. This translocon-proximal scaffold prevents STT3A from recognizing sequons in HSP90B1 and also sterically prevents access of these sequons to OST-B during folding. See fig.S10.</div>
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<h2 class="title">
Related information
</h2>
<ul class="related-links-list"><li><a title="Link to related Genes" href="https://www.ncbi.nlm.nih.gov/gene?linkname=pubmed_gene&amp;from_uid=39509507"
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Gene
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MedGen
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Nucleotide
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OMIM (cited)
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Protein
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Protein (RefSeq)
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<h2 class="title">
Grants and funding
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