Literature DB >> 6318797

Dutch beta 0-thalassaemia: a 10 kilobase DNA deletion associated with significant gamma-chain production.

J G Gilman, T H Huisman, J Abels.   

Abstract

A unique beta 0-thalassaemia in a Dutch family results in fetal haemoglobin expression comparable to that of delta 0 beta 0-thalassaemia. Haemoglobin analysis and restriction endonuclease mapping studies of DNA suggest that the beta-globin gene is entirely deleted, but that the delta-globin gene is intact. The 5' break point of the deletion is 3-4 kilobases 3' to the delta-globin gene, while the 3' break point is 6-7 kilobases 3' to the beta-globin gene (relative to the normal DNA restriction map). The result is a approximately 10 kilobase deletion of DNA whose 3' end point may lie very close to that for one delta 0 beta 0-thalassaemia, within a cluster of Kpn I-family repetitive sequences. The Dutch beta 0-thalassaemia deletion is thus the shortest one which, in the absence of additional chromosomal rearrangements, results in enhancement of gamma-chain synthesis above that seen for haemoglobin Lepore. These data support the hypothesis that the region of DNA 3' to the beta-globin gene may be important to the developmental regulation of fetal gamma versus adult beta chain production.

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Year:  1984        PMID: 6318797     DOI: 10.1111/j.1365-2141.1984.tb03961.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN: 0007-1048            Impact factor:   6.998


  13 in total

1.  The frequency of the gamma chain variant A gamma T in different populations, and its use in evaluating gamma gene expression in association with thalassemia.

Authors:  T H Huisman; F Kutlar; T Nakatsuji; A Bruce-Tagoe; Y Kilinç; M N Cauchi; C Romero Garcia
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

2.  A silent deletion in the beta-globin gene cluster.

Authors:  V E Tate; A V Hill; D K Bowden; J R Sadler; D J Weatherall; J B Clegg
Journal:  Nucleic Acids Res       Date:  1986-06-25       Impact factor: 16.971

3.  One haplotype is associated with the Swiss type of hereditary persistence of fetal hemoglobin in the Yugoslavian population.

Authors:  G D Efremov; I Gjorgovski; N Stojanovski; J C Diaz-Chico; T Harano; F Kutlar; T H Huisman
Journal:  Hum Genet       Date:  1987-10       Impact factor: 4.132

4.  Distal CCAAT box deletion in the A gamma globin gene of two black adolescents with elevated fetal A gamma globin.

Authors:  J G Gilman; N Mishima; X J Wen; T A Stoming; J Lobel; T H Huisman
Journal:  Nucleic Acids Res       Date:  1988-11-25       Impact factor: 16.971

5.  A beta-thalassemia mutant caused by a 300-bp deletion in the human beta-globin gene.

Authors:  C Aulehla-Scholz; R Spiegelberg; J Horst
Journal:  Hum Genet       Date:  1989-02       Impact factor: 4.132

6.  Molecular characterization of an atypical beta-thalassemia caused by a large deletion in the 5' beta-globin gene region.

Authors:  B W Popovich; D S Rosenblatt; A G Kendall; Y Nishioka
Journal:  Am J Hum Genet       Date:  1986-12       Impact factor: 11.025

7.  Characteristics of beta A chromosome haplotypes in Japanese.

Authors:  K Shimizu
Journal:  Biochem Genet       Date:  1987-04       Impact factor: 1.890

8.  The in vivo expression of the globin genes of the beta cistron in gamma-, delta-, and delta beta-thalassemia heterozygotes.

Authors:  A J Dimovski; A D Adekile; T H Huisman
Journal:  Experientia       Date:  1994-02-15

Review 9.  DNA polymorphism and molecular pathology of the human globin gene clusters.

Authors:  S E Antonarakis; H H Kazazian; S H Orkin
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

10.  Abnormal arrangements in the alpha- and gamma-globin gene clusters in a relatively large group of Japanese newborns.

Authors:  K Shimizu; T Harano; K Harano; S Miwa; Y Amenomori; Y Ohba; F Kutlar; T H Huisman
Journal:  Am J Hum Genet       Date:  1986-01       Impact factor: 11.025

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