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dc.contributor.authorZhao, Lei
dc.contributor.authorHou, Yuqing
dc.contributor.authorPicariello, Tyler
dc.contributor.authorCraige, Branch
dc.contributor.authorWitman, George B.
dc.date2022-08-11T08:10:48.000
dc.date.accessioned2022-08-23T17:20:43Z
dc.date.available2022-08-23T17:20:43Z
dc.date.issued2019-06-03
dc.date.submitted2019-06-12
dc.identifier.citation<p>J Cell Biol. 2019 Jun 3;218(6):2051-2070. doi: 10.1083/jcb.201902017. Epub 2019 May 15. <a href="https://doi.org/10.1083/jcb.201902017">Link to article on publisher's site</a></p>
dc.identifier.issn0021-9525 (Linking)
dc.identifier.doi10.1083/jcb.201902017
dc.identifier.pmid31092556
dc.identifier.urihttp://hdl.handle.net/20.500.14038/48362
dc.description.abstractNearly all motile cilia have a "9+2" axoneme containing a central apparatus (CA), consisting of two central microtubules with projections, that is essential for motility. To date, only 22 proteins are known to be CA components. To identify new candidate CA proteins, we used mass spectrometry to compare axonemes of wild-type Chlamydomonas and a CA-less mutant. We identified 44 novel candidate CA proteins, of which 13 are conserved in humans. Five of the latter were studied more closely, and all five localized to the CA; therefore, most of the other candidates are likely to also be CA components. Our results reveal that the CA is far more compositionally complex than previously recognized and provide a greatly expanded knowledge base for studies to understand the architecture of the CA and how it functions. The discovery of the new conserved CA proteins will facilitate genetic screening to identify patients with a form of primary ciliary dyskinesia that has been difficult to diagnose.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=31092556&dopt=Abstract">Link to Article in PubMed</a></p>
dc.rights© 2019 Zhao et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/
dc.subjectDisease
dc.subjectCilia
dc.subjectAmino Acids, Peptides, and Proteins
dc.subjectCell Biology
dc.subjectCells
dc.subjectCellular and Molecular Physiology
dc.subjectDiagnosis
dc.subjectGenetic Phenomena
dc.titleProteome of the central apparatus of a ciliary axoneme
dc.typeJournal Article
dc.source.journaltitleThe Journal of cell biology
dc.source.volume218
dc.source.issue6
dc.identifier.legacyfulltexthttps://escholarship.umassmed.edu/cgi/viewcontent.cgi?article=1481&amp;context=radiology_pubs&amp;unstamped=1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/radiology_pubs/471
dc.identifier.contextkey14725358
refterms.dateFOA2022-08-23T17:20:43Z
html.description.abstract<p>Nearly all motile cilia have a "9+2" axoneme containing a central apparatus (CA), consisting of two central microtubules with projections, that is essential for motility. To date, only 22 proteins are known to be CA components. To identify new candidate CA proteins, we used mass spectrometry to compare axonemes of wild-type Chlamydomonas and a CA-less mutant. We identified 44 novel candidate CA proteins, of which 13 are conserved in humans. Five of the latter were studied more closely, and all five localized to the CA; therefore, most of the other candidates are likely to also be CA components. Our results reveal that the CA is far more compositionally complex than previously recognized and provide a greatly expanded knowledge base for studies to understand the architecture of the CA and how it functions. The discovery of the new conserved CA proteins will facilitate genetic screening to identify patients with a form of primary ciliary dyskinesia that has been difficult to diagnose.</p>
dc.identifier.submissionpathradiology_pubs/471
dc.contributor.departmentWitman Lab
dc.contributor.departmentDivision of Cell Biology and Imaging, Department of Radiology
dc.source.pages2051-2070


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© 2019 Zhao et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0
International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
Except where otherwise noted, this item's license is described as © 2019 Zhao et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).