Literature DB >> 2364173

Alpha-thalassemia caused by a large (62 kb) deletion upstream of the human alpha globin gene cluster.

C S Hatton1, A O Wilkie, H C Drysdale, W G Wood, M A Vickers, J Sharpe, H Ayyub, I M Pretorius, V J Buckle, D R Higgs.   

Abstract

We describe a family in which alpha-thalassemia occurs in association with a deletion of 62 kilobases from a region upstream of the alpha globin genes. DNA sequence analysis has shown that the transcription units of both alpha genes downstream of this deletion are normal. Nevertheless, they fail to direct alpha globin synthesis in an interspecific hybrid containing the abnormal (alpha alpha)RA chromosome. It seems probable that previously unidentified positive regulatory sequences analogous to those detected in a corresponding position of the human beta globin cluster are removed by this deletion.

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Year:  1990        PMID: 2364173

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  22 in total

1.  Inactivation of human alpha-globin gene expression by a de novo deletion located upstream of the alpha-globin gene cluster.

Authors:  S A Liebhaber; E U Griese; I Weiss; F E Cash; H Ayyub; D R Higgs; J Horst
Journal:  Proc Natl Acad Sci U S A       Date:  1990-12       Impact factor: 11.205

2.  Characterization of the major regulatory element upstream of the human alpha-globin gene cluster.

Authors:  A P Jarman; W G Wood; J A Sharpe; G Gourdon; H Ayyub; D R Higgs
Journal:  Mol Cell Biol       Date:  1991-09       Impact factor: 4.272

Review 3.  Transcriptional mechanisms underlying hemoglobin synthesis.

Authors:  Koichi R Katsumura; Andrew W DeVilbiss; Nathaniel J Pope; Kirby D Johnson; Emery H Bresnick
Journal:  Cold Spring Harb Perspect Med       Date:  2013-09-01       Impact factor: 6.915

4.  A globin enhancer acts by increasing the proportion of erythrocytes expressing a linked transgene.

Authors:  H G Sutherland; D I Martin; E Whitelaw
Journal:  Mol Cell Biol       Date:  1997-03       Impact factor: 4.272

5.  Analysis of enhancer function of the HS-40 core sequence of the human alpha-globin cluster.

Authors:  H Chen; C H Lowrey; G Stamatoyannopoulos
Journal:  Nucleic Acids Res       Date:  1997-07-15       Impact factor: 16.971

6.  The molecular basis of α-thalassemia.

Authors:  Douglas R Higgs
Journal:  Cold Spring Harb Perspect Med       Date:  2013-01-01       Impact factor: 6.915

Review 7.  Decoding the non-coding genome: elucidating genetic risk outside the coding genome.

Authors:  C L Barr; V L Misener
Journal:  Genes Brain Behav       Date:  2016-01-04       Impact factor: 3.449

8.  Structure of the human 3-methyladenine DNA glycosylase gene and localization close to the 16p telomere.

Authors:  M A Vickers; P Vyas; P C Harris; D L Simmons; D R Higgs
Journal:  Proc Natl Acad Sci U S A       Date:  1993-04-15       Impact factor: 11.205

9.  Human alpha-globin gene expression is silenced by terminal truncation of chromosome 16p beginning immediately 3' of the zeta-globin gene.

Authors:  L Romao; F Cash; I Weiss; S Liebhaber; M Pirastu; R Galanello; A Loi; E Paglietti; P Ioannou; A Cao
Journal:  Hum Genet       Date:  1992-05       Impact factor: 4.132

10.  Complementation of alpha-thalassaemia in alpha-globin knockout mice with a 191 kb transgene containing the human alpha-globin locus.

Authors:  Keith Al-Hasani; Jim Vadolas; Lucille Voullaire; Robert Williamson; Panayiotis A Ioannou
Journal:  Transgenic Res       Date:  2004-06       Impact factor: 2.788

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