Literature DB >> 12737310

Dyskeratosis congenita.

A Marrone1, P J Mason.   

Abstract

Dyskeratosis congenita is an inherited skin and bone marrow failure syndrome. There are X-linked, autosomal dominant and autosomal recessive forms of the disease. The X-linked form is due to mutations in the DKC1 gene at Xq28. The encoded protein, dyskerin, is a component of both small nucleolar ribonuclear protein particles and the telomerase complex. Mutations in DKC1 mainly lead to amino acid substitutions. The autosomal dominant form of the disease is due to mutations in hTR, the RNA component of telomerase, making it likely that the disease is due to defective telomerase activity. Mutations in hTR are predicted to either disrupt secondary structure or alter the template region. The gene or genes involved in the recessive forms of the disease remain elusive, though genes whose products are required for telomere maintenance are strong candidates.

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Year:  2003        PMID: 12737310     DOI: 10.1007/s000180300042

Source DB:  PubMed          Journal:  Cell Mol Life Sci        ISSN: 1420-682X            Impact factor:   9.261


  16 in total

1.  The gastrointestinal manifestations of telomere-mediated disease.

Authors:  Naudia L Jonassaint; Nini Guo; Joseph A Califano; Elizabeth A Montgomery; Mary Armanios
Journal:  Aging Cell       Date:  2013-01-04       Impact factor: 9.304

2.  The accumulation and not the specific activity of telomerase ribonucleoprotein determines telomere maintenance deficiency in X-linked dyskeratosis congenita.

Authors:  Xi-Lei Zeng; Naresh R Thumati; Helen B Fleisig; Kyle R Hukezalie; Sharon A Savage; Neelam Giri; Blanche P Alter; Judy M Y Wong
Journal:  Hum Mol Genet       Date:  2011-11-04       Impact factor: 6.150

Review 3.  The many facets of H/ACA ribonucleoproteins.

Authors:  U Thomas Meier
Journal:  Chromosoma       Date:  2005-03-16       Impact factor: 4.316

4.  Dynamic association and localization of human H/ACA RNP proteins.

Authors:  Nupur Kittur; Xavier Darzacq; Sujayita Roy; Robert H Singer; U Thomas Meier
Journal:  RNA       Date:  2006-10-24       Impact factor: 4.942

Review 5.  Structures of ribonucleoprotein particle modification enzymes.

Authors:  Bo Liang; Hong Li
Journal:  Q Rev Biophys       Date:  2010-11-26       Impact factor: 5.318

Review 6.  It all comes together at the ends: telomerase structure, function, and biogenesis.

Authors:  Joshua D Podlevsky; Julian J-L Chen
Journal:  Mutat Res       Date:  2011-11-07       Impact factor: 2.433

7.  The Treacher Collins syndrome (TCOF1) gene product is involved in ribosomal DNA gene transcription by interacting with upstream binding factor.

Authors:  Benigno C Valdez; Dale Henning; Rolando B So; Jill Dixon; Michael J Dixon
Journal:  Proc Natl Acad Sci U S A       Date:  2004-07-12       Impact factor: 11.205

8.  Telomerase RNA deficiency in peripheral blood mononuclear cells in X-linked dyskeratosis congenita.

Authors:  Judy M Y Wong; Mouhammed J Kyasa; Laura Hutchins; Kathleen Collins
Journal:  Hum Genet       Date:  2004-09-03       Impact factor: 4.132

9.  Architecture and assembly of mammalian H/ACA small nucleolar and telomerase ribonucleoproteins.

Authors:  Chen Wang; U Thomas Meier
Journal:  EMBO J       Date:  2004-03-25       Impact factor: 11.598

10.  Defects in mTR stability and telomerase activity produced by the Dkc1 A353V mutation in dyskeratosis congenita are rescued by a peptide from the dyskerin TruB domain.

Authors:  Rosario Machado-Pinilla; Jaime Carrillo; Cristina Manguan-Garcia; Leandro Sastre; Alexander Mentzer; B-W Gu; Philip J Mason; Rosario Perona
Journal:  Clin Transl Oncol       Date:  2012-07-24       Impact factor: 3.405

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