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


Autoria(s): Anderson B.H.; Kasher P.R.; Mayer J.; Szynkiewicz M.; Jenkinson E.M.; Bhaskar S.S.; Urquhart J.E.; Daly S.B.; Dickerson J.E.; O'Sullivan J.; Leibundgut E.O.; Muter J.; Abdel-Salem G.M.; Babul-Hirji R.; Baxter P.; Berger A.; Bonafé L.; Brunstom-Hernandez J.E.; Buckard J.A.; Chitayat D.; Chong W.K.; Cordelli D.M.; Ferreira P.; Fluss J.; Forrest E.H.; Franzoni E.; Garone C.; Hammans S.R.; Houge G.; Hughes I.; Jacquemont S.; Jeannet P.Y.; Jefferson R.J.; Kumar R.; Kutschke G.; Lundberg S.; Lourenço C.M.; Mehta R.; Naidu S.; Nischal K.K.; Nunes L.; Ounap K.; Philippart M.; Prabhakar P.; Risen S.R.; Schiffmann R.; Soh C.; Stephenson J.B.; Stewart H.; Stone J.; Tolmie J.L.; van der Knaap M.S.; Vieira J.P.; Vilain C.N.; Wakeling E.L.; Wermenbol V.; Whitney A.; Lovell S.C.; Meyer S.; Livingston J.H.; Baerlocher G.M.; Black G.C.; Rice G.I.; Crow Y.J.
Data(s)

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 γH2AX-positive cells in cell lines derived from two affected individuals. CTC1 is also a subunit of the α-accessory factor (AAF) complex, stimulating the activity of DNA polymerase-α 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.

Identificador

http://serval.unil.ch/?id=serval:BIB_9DCDA709F4F3

isbn:1546-1718 (Electronic)

pmid:22267198

doi:10.1038/ng.1084

isiid:000300843600023

Idioma(s)

en

Fonte

Nature Genetics, vol. 44, no. 3, pp. 338-342

Tipo

info:eu-repo/semantics/article

article