Literature DB >> 6305443

The delta beta crossover region in Lepore boston hemoglobinopathy is restricted to a 59 base pairs region around the 5' splice junction of the large globin gene intervening sequence.

F Mavilio, A Giampaolo, A Caré, N M Sposi, M Marinucci.   

Abstract

Genomic DNA from a hemoglobin (Hb) Lepore Boston (delta 87 Gln beta 116 His) homozygote of Southern Italian origin has been studied in order to map the fusion point between the delta and beta genes. An Ava II restriction endonuclease recognition sequence, located 12 base pairs (bp) downstream from the 5' end of the beta gene large intervening sequence, has been taken as marker of the beta-like portion of the fusion gene. This site was present even in the delta beta gene, allowing the localization of the crossover area to a 59-bp region extending from the first nucleotide of the Leu codon in position 88 to the 11th nucleotide of the large intervening sequence. The analysis of the DNA restriction polymorphisms in the gamma delta beta globin gene region provides evidence that a single mutational event originated the Lepore delta beta genes, at least in the Italian population.

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Year:  1983        PMID: 6305443

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


  8 in total

1.  Origin heterogeneity of Hb Lepore-Boston gene in Italy.

Authors:  G Fioretti; M De Angioletti; F Masciangelo; G Lacerra; A Scarallo; C de Bonis; L Pagano; E Guarino; L De Rosa; F Salvati
Journal:  Am J Hum Genet       Date:  1992-04       Impact factor: 11.025

2.  Characterization of chromosomes with hybrid genes for Hb Lepore-Washington, Hb Lepore-Baltimore, Hb P-Nilotic, and Hb Kenya.

Authors:  K D Lanclos; J Patterson; G D Efremov; S C Wong; A Villegas; P J Ojwang; J B Wilson; F Kutlar; T H Huisman
Journal:  Hum Genet       Date:  1987-09       Impact factor: 4.132

3.  Heterocellular hereditary persistence of fetal hemoglobin (HPFH). Molecular mechanisms of abnormal gamma-gene expression in association with beta thalassemia and linkage relationship with the beta-globin gene cluster.

Authors:  A Giampaolo; F Mavilio; N M Sposi; A Carè; A Massa; L Cianetti; M Petrini; R Russo; M D Cappellini; M Marinucci
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

4.  Association of heterocellular HPFH, beta(+)-thalassaemia, and delta beta(0)-thalassaemia: haematological and molecular aspects.

Authors:  L Cianetti; A Care; N M Sposi; A Giampaolo; M Calandrini; M Petrini; A Massa; M Marinucci; F Mavilio; M Ceccanti
Journal:  J Med Genet       Date:  1984-08       Impact factor: 6.318

5.  Delta beta-thalassaemia in southern Italy: evidence for a single mutational event.

Authors:  A Carè; N M Sposi; A Giampaolo; T Improta; M Calandrini; M Petrini; M Marinucci; A Tagarelli; C Brancati
Journal:  J Med Genet       Date:  1984-04       Impact factor: 6.318

6.  Molecular mechanisms of human hemoglobin switching: selective undermethylation and expression of globin genes in embryonic, fetal, and adult erythroblasts.

Authors:  F Mavilio; A Giampaolo; A Carè; G Migliaccio; M Calandrini; G Russo; G L Pagliardi; G Mastroberardino; M Marinucci; C Peschle
Journal:  Proc Natl Acad Sci U S A       Date:  1983-11       Impact factor: 11.205

7.  Origin and ascendancy of a chimeric fusion gene: the beta/delta-globin gene of paenungulate mammals.

Authors:  Juan C Opazo; Angela M Sloan; Kevin L Campbell; Jay F Storz
Journal:  Mol Biol Evol       Date:  2009-03-30       Impact factor: 16.240

8.  A beta-globin gene, inactive in the K562 leukemic cell, functions normally in a heterologous expression system.

Authors:  C M Fordis; N P Anagnou; A Dean; A W Nienhuis; A N Schechter
Journal:  Proc Natl Acad Sci U S A       Date:  1984-07       Impact factor: 11.205

  8 in total

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