Literature DB >> 9863595

1.4 Mb candidate gene region for X linked dyskeratosis congenita defined by combined haplotype and X chromosome inactivation analysis.

S W Knight1, T J Vulliamy, N S Heiss, G Matthijs, K Devriendt, J M Connor, M D'Urso, A Poustka, P J Mason, I Dokal.   

Abstract

Dyskeratosis congenita (DC) is a rare inherited disorder characterised by the early onset of reticulate skin pigmentation, nail dystrophy, and mucosal leucoplakia. In over 80% of cases bone marrow failure develops and this is the main cause of early mortality. The DC1 gene responsible for the X linked form (MIM 305000) of dyskeratosis congenita has been mapped to Xq28. In order to narrow the candidate gene region, genetic linkage analysis was performed in eight X linked pedigrees using a set of markers spanning Xq28. A maximum lod score of 5.31 with no recombinations was achieved with marker DXS1073. Two recombination events were identified; one of these uses X chromosome inactivation pattern analysis to determine carrier status and haplotype analysis to fine map the recombination breakpoint. The fine mapping of these recombination events has enabled the candidate gene region for X linked dyskeratosis congenita to be defined as the 1.4 Mb interval between Xq3274 and DXS1108.

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Year:  1998        PMID: 9863595      PMCID: PMC1051510          DOI: 10.1136/jmg.35.12.993

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  19 in total

Review 1.  Genetic control of X inactivation and processes leading to X-inactivation skewing.

Authors:  J W Belmont
Journal:  Am J Hum Genet       Date:  1996-06       Impact factor: 11.025

2.  Transcriptional analysis of the candidate region for incontinentia pigmenti (IP2) in Xq28.

Authors:  U C Rogner; N S Heiss; P Kioschis; S Wiemann; B Korn; A Poustka
Journal:  Genome Res       Date:  1996-10       Impact factor: 9.043

Review 3.  Dyskeratosis congenita: an inherited bone marrow failure syndrome.

Authors:  I Dokal
Journal:  Br J Haematol       Date:  1996-03       Impact factor: 6.998

4.  The sequence organization of the long arm pseudoautosomal region of the human sex chromosomes.

Authors:  K Kvaløy; F Galvagni; W R Brown
Journal:  Hum Mol Genet       Date:  1994-05       Impact factor: 6.150

5.  G6PD haplotypes spanning Xq28 from F8C to red/green color vision.

Authors:  S Filosa; V Calabrò; G Lania; T J Vulliamy; C Brancati; A Tagarelli; L Luzzatto; G Martini
Journal:  Genomics       Date:  1993-07       Impact factor: 5.736

6.  Transcription mapping in a 700-kb region around the DXS52 locus in Xq28: isolation of six novel transcripts and a novel ATPase isoform (hPMCA5).

Authors:  N S Heiss; U C Rogner; P Kioschis; B Korn; A Poustka
Journal:  Genome Res       Date:  1996-06       Impact factor: 9.043

7.  Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation.

Authors:  R C Allen; H Y Zoghbi; A B Moseley; H M Rosenblatt; J W Belmont
Journal:  Am J Hum Genet       Date:  1992-12       Impact factor: 11.025

8.  Origin and spread of the glucose-6-phosphate dehydrogenase variant (G6PD-Mediterranean) in the Middle East.

Authors:  B Kurdi-Haidar; P J Mason; A Berrebi; G Ankra-Badu; A al-Ali; A Oppenheim; L Luzzatto
Journal:  Am J Hum Genet       Date:  1990-12       Impact factor: 11.025

9.  X-linked dyskeratosis congenita with pancytopenia.

Authors:  A Gutman; A Frumkin; A Adam; N Bloch-Shtacher; L A Rozenszajn
Journal:  Arch Dermatol       Date:  1978-11

10.  Long-range sequence analysis in Xq28: thirteen known and six candidate genes in 219.4 kb of high GC DNA between the RCP/GCP and G6PD loci.

Authors:  E Y Chen; M Zollo; R Mazzarella; A Ciccodicola; C N Chen; L Zuo; C Heiner; F Burough; M Repetto; D Schlessinger; M D'Urso
Journal:  Hum Mol Genet       Date:  1996-05       Impact factor: 6.150

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  12 in total

Review 1.  The genetics of dyskeratosis congenita.

Authors:  Philip J Mason; Monica Bessler
Journal:  Cancer Genet       Date:  2011-12

2.  mRNA deadenylation and telomere disease.

Authors:  Philip J Mason; Monica Bessler
Journal:  J Clin Invest       Date:  2015-04-20       Impact factor: 14.808

3.  Exome sequencing identifies MPL as a causative gene in familial aplastic anemia.

Authors:  Amanda J Walne; Arran Dokal; Vincent Plagnol; Richard Beswick; Michael Kirwan; Josu de la Fuente; Tom Vulliamy; Inderjeet Dokal
Journal:  Haematologica       Date:  2011-12-16       Impact factor: 9.941

Review 4.  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

5.  X-linked dyskeratosis congenita is predominantly caused by missense mutations in the DKC1 gene.

Authors:  S W Knight; N S Heiss; T J Vulliamy; S Greschner; G Stavrides; G S Pai; G Lestringant; N Varma; P J Mason; I Dokal; A Poustka
Journal:  Am J Hum Genet       Date:  1999-07       Impact factor: 11.025

6.  X inactivation testing for identifying a non-syndromic X-linked mental retardation gene.

Authors:  Hagith Yonath; Dina Marek-Yagel; Haike Resnik-Wolf; Almogit Abu-Horvitz; Hagit N Baris; Mordechai Shohat; Moshe Frydman; Elon Pras
Journal:  J Appl Genet       Date:  2011-05-17       Impact factor: 3.240

7.  Intensive immunosuppression therapy for aplastic anemia associated with dyskeratosis congenita: report of a case.

Authors:  Patrizia Comoli; Sabrina Basso; Guan-Cheng Huanga
Journal:  Int J Hematol       Date:  2005-07       Impact factor: 2.490

Review 8.  Evaluation and Management of Hematopoietic Failure in Dyskeratosis Congenita.

Authors:  Suneet Agarwal
Journal:  Hematol Oncol Clin North Am       Date:  2018-05-28       Impact factor: 3.722

Review 9.  Molecular basis of telomere dysfunction in human genetic diseases.

Authors:  Grzegorz Sarek; Paulina Marzec; Pol Margalef; Simon J Boulton
Journal:  Nat Struct Mol Biol       Date:  2015-11       Impact factor: 15.369

Review 10.  Unraveling the pathogenesis of Hoyeraal-Hreidarsson syndrome, a complex telomere biology disorder.

Authors:  Galina Glousker; Fabien Touzot; Patrick Revy; Yehuda Tzfati; Sharon A Savage
Journal:  Br J Haematol       Date:  2015-05-04       Impact factor: 6.998

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