Literature DB >> 22267198

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

Beverley H Anderson1, Paul R Kasher, Josephine Mayer, Marcin Szynkiewicz, Emma M Jenkinson, Sanjeev S Bhaskar, Jill E Urquhart, Sarah B Daly, Jonathan E Dickerson, James O'Sullivan, Elisabeth Oppliger Leibundgut, Joanne Muter, Ghada M H Abdel-Salem, Riyana Babul-Hirji, Peter Baxter, Andrea Berger, Luisa Bonafé, Janice E Brunstom-Hernandez, Johannes A Buckard, David Chitayat, Wui K Chong, Duccio M Cordelli, Patrick Ferreira, Joel Fluss, Ewan H Forrest, Emilio Franzoni, Caterina Garone, Simon R Hammans, Gunnar Houge, Imelda Hughes, Sebastien Jacquemont, Pierre-Yves Jeannet, Rosalind J Jefferson, Ram Kumar, Georg Kutschke, Staffan Lundberg, Charles M Lourenço, Ramesh Mehta, Sakkubai Naidu, Ken K Nischal, Luís Nunes, Katrin Ounap, Michel Philippart, Prab Prabhakar, Sarah R Risen, Raphael Schiffmann, Calvin Soh, John B P Stephenson, Helen Stewart, Jon Stone, John L Tolmie, Marjo S van der Knaap, Jose P Vieira, Catheline N Vilain, Emma L Wakeling, Vanessa Wermenbol, Andrea Whitney, Simon C Lovell, Stefan Meyer, John H Livingston, Gabriela M Baerlocher, Graeme C M Black, Gillian I Rice, Yanick J Crow.   

Abstract

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.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22267198     DOI: 10.1038/ng.1084

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  18 in total

Review 1.  CST meets shelterin to keep telomeres in check.

Authors:  Marie-Josèphe Giraud-Panis; M Teresa Teixeira; Vincent Géli; Eric Gilson
Journal:  Mol Cell       Date:  2010-09-10       Impact factor: 17.970

Review 2.  Evolution of CST function in telomere maintenance.

Authors:  Carolyn M Price; Kara A Boltz; Mary F Chaiken; Jason A Stewart; Mark A Beilstein; Dorothy E Shippen
Journal:  Cell Cycle       Date:  2010-08-26       Impact factor: 4.534

3.  Cerebroretinal microangiopathy with calcifications and cysts.

Authors:  T Linnankivi; L Valanne; A Paetau; I Alafuzoff; J M Hakumäki; T Kivelä; T Lönnqvist; O Mäkitie; L Pääkkönen; L Vainionpää; R Vanninen; R Herva; H Pihko
Journal:  Neurology       Date:  2006-08-30       Impact factor: 9.910

4.  A familial syndrome with coats' reaction retinal angiomas, hair and nail defects and intracranial calcification.

Authors:  J L Tolmie; B H Browne; P M McGettrick; J B Stephenson
Journal:  Eye (Lond)       Date:  1988       Impact factor: 3.775

Review 5.  Dyskeratosis congenita as a disorder of telomere maintenance.

Authors:  Nya D Nelson; Alison A Bertuch
Journal:  Mutat Res       Date:  2011-07-02       Impact factor: 2.433

6.  Extensive brain calcifications, leukodystrophy, and formation of parenchymal cysts: a new progressive disorder due to diffuse cerebral microangiopathy.

Authors:  P Labrune; C Lacroix; F Goutières; J de Laveaucoupet; P Chevalier; M Zerah; B Husson; P Landrieu
Journal:  Neurology       Date:  1996-05       Impact factor: 9.910

7.  Treatment of Gastrointestinal Bleeding in a Probable Case of Cerebroretinal Microangiopathy with Calcifications and Cysts.

Authors:  T A Briggs; M Hubbard; C Hawkins; T Cole; J H Livingston; Y J Crow; A Pigott
Journal:  Mol Syndromol       Date:  2010-11-09

8.  Leukoencephalopathy, cerebral calcifications, and cysts: new observations.

Authors:  L M Nagae-Poetscher; G Bibat; M Philippart; S Rosemberg; A Fatemi; M T C Lacerda; M O R Costa; F Kok; C Costa Leite; A Horská; P B Barker; S Naidu
Journal:  Neurology       Date:  2004-04-13       Impact factor: 9.910

9.  Coats' plus: a progressive familial syndrome of bilateral Coats' disease, characteristic cerebral calcification, leukoencephalopathy, slow pre- and post-natal linear growth and defects of bone marrow and integument.

Authors:  Y J Crow; J McMenamin; C A Haenggeli; D M Hadley; S Tirupathi; E P Treacy; S M Zuberi; B H Browne; J L Tolmie; J B P Stephenson
Journal:  Neuropediatrics       Date:  2004-02       Impact factor: 1.947

10.  Conserved telomere maintenance component 1 interacts with STN1 and maintains chromosome ends in higher eukaryotes.

Authors:  Yulia V Surovtseva; Dmitri Churikov; Kara A Boltz; Xiangyu Song; Jonathan C Lamb; Ross Warrington; Katherine Leehy; Michelle Heacock; Carolyn M Price; Dorothy E Shippen
Journal:  Mol Cell       Date:  2009-10-23       Impact factor: 17.970

View more
  109 in total

1.  Connecting complex disorders through biology.

Authors:  Sharon A Savage
Journal:  Nat Genet       Date:  2012-02-27       Impact factor: 38.330

Review 2.  The molecular genetics of the telomere biology disorders.

Authors:  Alison A Bertuch
Journal:  RNA Biol       Date:  2015-09-23       Impact factor: 4.652

Review 3.  Understanding telomere diseases through analysis of patient-derived iPS cells.

Authors:  Luis F Z Batista; Steven E Artandi
Journal:  Curr Opin Genet Dev       Date:  2013-08-28       Impact factor: 5.578

4.  Human TEN1 maintains telomere integrity and functions in genome-wide replication restart.

Authors:  Christopher Kasbek; Feng Wang; Carolyn M Price
Journal:  J Biol Chem       Date:  2013-09-11       Impact factor: 5.157

5.  CTC1 Mutations in a patient with dyskeratosis congenita.

Authors:  Rachel B Keller; Katelyn E Gagne; G Naheed Usmani; George K Asdourian; David A Williams; Inga Hofmann; Suneet Agarwal
Journal:  Pediatr Blood Cancer       Date:  2012-04-24       Impact factor: 3.167

6.  CTC1 deletion results in defective telomere replication, leading to catastrophic telomere loss and stem cell exhaustion.

Authors:  Peili Gu; Jin-Na Min; Yang Wang; Chenhui Huang; Tao Peng; Weihang Chai; Sandy Chang
Journal:  EMBO J       Date:  2012-04-24       Impact factor: 11.598

7.  Telomere-end processing: mechanisms and regulation.

Authors:  Diego Bonetti; Marina Martina; Marco Falcettoni; Maria Pia Longhese
Journal:  Chromosoma       Date:  2013-10-12       Impact factor: 4.316

8.  Sequential phosphorylation of CST subunits by different cyclin-Cdk1 complexes orchestrate telomere replication.

Authors:  Veena Gopalakrishnan; Cherylin Ruiling Tan; Shang Li
Journal:  Cell Cycle       Date:  2017-06-26       Impact factor: 4.534

9.  Human CST Prefers G-Rich but Not Necessarily Telomeric Sequences.

Authors:  Robert A Hom; Deborah S Wuttke
Journal:  Biochemistry       Date:  2017-08-02       Impact factor: 3.162

10.  Tying up the Ends: Plasticity in the Recognition of Single-Stranded DNA at Telomeres.

Authors:  Neil R Lloyd; Thayne H Dickey; Robert A Hom; Deborah S Wuttke
Journal:  Biochemistry       Date:  2016-09-15       Impact factor: 3.162

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.