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Mutations in CTC1, ...
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Anderson, Beverley H.
(author)
Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus
- Article/chapterEnglish2012
Publisher, publication year, extent ...
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2012-01-22
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Springer Science and Business Media LLC,2012
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printrdacarrier
Numbers
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LIBRIS-ID:oai:DiVA.org:uu-171658
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https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-171658URI
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https://doi.org/10.1038/ng.1084DOI
Supplementary language notes
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Language:English
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Summary in:English
Part of subdatabase
Classification
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Subject category:ref swepub-contenttype
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Subject category:art swepub-publicationtype
Notes
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Coats plus is a highly pleiotropic disorder particularly affecting the eye, brain, bone and gastrointestinal tract. Here, we show that Coats plus results from mutations in CTC1, encoding conserved telomere maintenance component 1, a member of the mammalian homolog of the yeast heterotrimeric CST telomeric capping complex. Consistent with the observation of shortened telomeres in an Arabidopsis CTC1 mutant and the phenotypic overlap of Coats plus with the telomeric maintenance disorders comprising dyskeratosis congenita, we observed shortened telomeres in three individuals with Coats plus and an increase in spontaneous gamma H2AX-positive cells in cell lines derived from two affected individuals. CTC1 is also a subunit of the alpha-accessory factor (AAF) complex, stimulating the activity of DNA polymerase-alpha primase, the only enzyme known to initiate DNA replication in eukaryotic cells. Thus, CTC1 may have a function in DNA metabolism that is necessary for but not specific to telomeric integrity.
Added entries (persons, corporate bodies, meetings, titles ...)
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Kasher, Paul R.
(author)
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Mayer, Josephine
(author)
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Szynkiewicz, Marcin
(author)
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Jenkinson, Emma M.
(author)
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Bhaskar, Sanjeev S.
(author)
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Urquhart, Jill E.
(author)
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Daly, Sarah B.
(author)
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Dickerson, Jonathan E.
(author)
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O'Sullivan, James
(author)
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Leibundgut, Elisabeth Oppliger
(author)
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Muter, Joanne
(author)
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Abdel-Salem, Ghada M. H.
(author)
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Babul-Hirji, Riyana
(author)
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Baxter, Peter
(author)
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Berger, Andrea
(author)
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Bonafe, Luisa
(author)
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Brunstom-Hernandez, Janice E.
(author)
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Buckard, Johannes A.
(author)
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Chitayat, David
(author)
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Chong, Wui K.
(author)
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Cordelli, Duccio M.
(author)
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Ferreira, Patrick
(author)
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Fluss, Joel
(author)
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Forrest, Ewan H.
(author)
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Franzoni, Emilio
(author)
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Garone, Caterina
(author)
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Hammans, Simon R.
(author)
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Houge, Gunnar
(author)
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Hughes, Imelda
(author)
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Jacquemont, Sebastien
(author)
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Jeannet, Pierre-Yves
(author)
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Jefferson, Rosalind J.
(author)
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Kumar, Ram
(author)
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Kutschke, Georg
(author)
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Lundberg, Staffan,1956-Uppsala universitet,Institutionen för kvinnors och barns hälsa,Barnneurologisk forskning/Ahlsten(Swepub:uu)staflund
(author)
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Lourenco, Charles M.
(author)
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Mehta, Ramesh
(author)
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Naidu, Sakkubai
(author)
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Nischal, Ken K.
(author)
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Nunes, Luis
(author)
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Ounap, Katrin
(author)
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Philippart, Michel
(author)
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Prabhakar, Prab
(author)
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Risen, Sarah R.
(author)
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Schiffmann, Raphael
(author)
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Soh, Calvin
(author)
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Stephenson, John B. P.
(author)
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Stewart, Helen
(author)
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Stone, Jon
(author)
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Tolmie, John L.
(author)
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van der Knaap, Marjo S.
(author)
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Vieira, Jose P.
(author)
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Vilain, Catheline N.
(author)
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Wakeling, Emma L.
(author)
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Wermenbol, Vanessa
(author)
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Whitney, Andrea
(author)
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Lovell, Simon C.
(author)
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Meyer, Stefan
(author)
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Livingston, John H.
(author)
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Baerlocher, Gabriela M.
(author)
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Black, Graeme C. M.
(author)
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Rice, Gillian I.
(author)
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Crow, Yanick J.
(author)
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Uppsala universitetInstitutionen för kvinnors och barns hälsa
(creator_code:org_t)
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In:Nature Genetics: Springer Science and Business Media LLC44:3, s. 338-3421061-40361546-1718
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Anderson, Beverl ...
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Jenkinson, Emma ...
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Nature Genetics
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Uppsala University