Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus


Autoria(s): Anderson, Beverley H.; Kasher, Paul R.; Mayer, Josephine; Szynkiewicz, Marcin; Jenkinson, Emma M.; Bhaskar, Sanjeev S.; Urquhart, Jill E.; Daly, Sarah B.; Dickerson, Jonathan E.; O'Sullivan, James; Leibundgut, Elisabeth Oppliger; Muter, Joanne; Abdel-Salem, Ghada M. H.; Babul-Hirji, Riyana; Baxter, Peter; Berger, Andrea; Bonafe, Luisa; Brunstom-Hernandez, Janice E.; Buckard, Johannes A.; Chitayat, David; Chong, Wui K.; Cordelli, Duccio M.; Ferreira, Patrick; Fluss, Joel; Forrest, Ewan H.; Franzoni, Emilio; Garone, Caterina; Hammans, Simon R.; Houge, Gunnar; Hughes, Imelda; Jacquemont, Sebastien; Jeannet, Pierre-Yves; Jefferson, Rosalind J.; Kumar, Ram; Kutschke, Georg; Lundberg, Staffan; Lourenco, Charles M.; Mehta, Ramesh; Naidu, Sakkubai; Nischal, Ken K.; Nunes, Luis; Ounap, Katrin; Philippart, Michel; Prabhakar, Prab; Risen, Sarah R.; Schiffmann, Raphael; Soh, Calvin; Stephenson, John B. P.; Stewart, Helen; Stone, Jon; Tolmie, John L.; van der Knaap, Marjo S.; Vieira, Jose P.; Vilain, Catheline N.; Wakeling, Emma L.; Wermenbol, Vanessa; Whitney, Andrea; Lovell, Simon C.; Meyer, Stefan; Livingston, John H.; Baerlocher, Gabriela M.; Black, Graeme C. M.; Rice, Gillian I.; Crow, Yanick J.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

05/11/2013

05/11/2013

2012

Resumo

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.

Great Ormond Street Hospital Children's Charity

Great Ormond Street Hospital Childrens Charity

Newlife Foundation

Newlife Foundation

Identificador

NATURE GENETICS, NEW YORK, v. 44, n. 3, supl. 4, Part 1-2, pp. 338-U1604, MAR, 2012

1061-4036

http://www.producao.usp.br/handle/BDPI/41747

10.1038/ng.1084

http://dx.doi.org/10.1038/ng.1084

Idioma(s)

eng

Publicador

NATURE PUBLISHING GROUP

NEW YORK

Relação

NATURE GENETICS

Direitos

closedAccess

Copyright NATURE PUBLISHING GROUP

Palavras-Chave #CEREBRORETINAL MICROANGIOPATHY #FAMILIAL SYNDROME #CALCIFICATIONS #CYSTS #PROTEIN #DNA #LEUKOENCEPHALOPATHY #EVOLUTION #DEFECTS #GENETICS & HEREDITY
Tipo

article

original article

publishedVersion