Literature DB >> 6594559

Selective expression within the human alpha globin gene complex following chromosome-dependent transfer into diploid mouse erythroleukaemia cells.

H C Zeitlin, D J Weatherall.   

Abstract

Human chromosome 16, which contains the alpha globin gene complex, has been introduced into mouse erythroleukaemia cells by means of cell fusion and selectively retained to the exclusion of other human chromosomes. After induction of haemoglobin synthesis in hybrid clones, evidence for expression of the human alpha globin genes was sought by mRNA and globin chain synthesis analyses. It was found that both the human alpha 1 and alpha 2 genes were similarly expressed and that the synthesis of human alpha globin chains was nearly half that of mouse alpha chains on a per gene basis. The pattern of human alpha gene expression was similar with different inducers and with donor chromosomes of either erythroid or non-erythroid origin. However, the closely linked human embryonic alpha gene (zeta) did not produce detectable levels of zeta globin mRNA in any of the hybrid clones. Thus, there is selective activation of adult genes in the human alpha globin gene complex in the mouse erythroleukaemia cell.

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Year:  1983        PMID: 6594559

Source DB:  PubMed          Journal:  Mol Biol Med        ISSN: 0735-1313


  7 in total

1.  S1 nuclease analysis of alpha-globin gene expression in preleukemic patients with acquired hemoglobin H disease after transfer to mouse erythroleukemia cells.

Authors:  J Helder; A Deisseroth
Journal:  Proc Natl Acad Sci U S A       Date:  1987-04       Impact factor: 11.205

2.  In vivo footprinting of the human alpha-globin locus upstream regulatory element by guanine and adenine ligation-mediated polymerase chain reaction.

Authors:  E C Strauss; N C Andrews; D R Higgs; S H Orkin
Journal:  Mol Cell Biol       Date:  1992-05       Impact factor: 4.272

3.  De novo truncation of chromosome 16p and healing with (TTAGGG)n in the alpha-thalassemia/mental retardation syndrome (ATR-16).

Authors:  J Lamb; P C Harris; A O Wilkie; W G Wood; J G Dauwerse; D R Higgs
Journal:  Am J Hum Genet       Date:  1993-04       Impact factor: 11.025

4.  Clinical features and molecular analysis of the alpha thalassemia/mental retardation syndromes. II. Cases without detectable abnormality of the alpha globin complex.

Authors:  A O Wilkie; H C Zeitlin; R H Lindenbaum; V J Buckle; N Fischel-Ghodsian; D H Chui; D Gardner-Medwin; M H MacGillivray; D J Weatherall; D R Higgs
Journal:  Am J Hum Genet       Date:  1990-06       Impact factor: 11.025

5.  The LCR-like alpha-globin positive regulatory element functions as an enhancer in transiently transfected cells during erythroid differentiation.

Authors:  M D Pondel; M George; N J Proudfoot
Journal:  Nucleic Acids Res       Date:  1992-01-25       Impact factor: 16.971

6.  Healing of broken human chromosomes by the addition of telomeric repeats.

Authors:  J Flint; C F Craddock; A Villegas; D P Bentley; H J Williams; R Galanello; A Cao; W G Wood; H Ayyub; D R Higgs
Journal:  Am J Hum Genet       Date:  1994-09       Impact factor: 11.025

7.  ATR-16 syndrome: mechanisms linking monosomy to phenotype.

Authors:  Christian Babbs; Jill Brown; Sharon W Horsley; Joanne Slater; Evie Maifoshie; Shiwangini Kumar; Paul Ooijevaar; Marjolein Kriek; Amanda Dixon-McIver; Cornelis L Harteveld; Jan Traeger-Synodinos; Andrew O M Wilkie; Douglas R Higgs; Veronica J Buckle
Journal:  J Med Genet       Date:  2020-01-31       Impact factor: 6.318

  7 in total

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