Literature DB >> 8641705

Hb Costa Rica or alpha 2 beta 2 77(EF1)His --> Arg: the first example of a somatic cell mutation in a globin gene.

W E Rodriguez Romero1, M Castillo, M A Chaves, G F Saenz, L H Gu, J B Wilson, E Baysal, N S Smetanina, J Y Leonova, T H Huisman.   

Abstract

We have identified a minor hemoglobin component (approximately 5%) in the blood of a healthy Costa Rican female, but not in her mother and two brothers (father not studied), that has an His --> Arg replacement at position beta 77 (Hb Costa Rica). No other amino acid replacements were observed and no beta- or gamma-chain-like peptides were present. Hb Costa Rica has abnormal stability. Sequence analyses of numerous polymerase chain reaction (PCR)-amplified segments of DNA that contain exon 2 of the beta gene failed to identify a CAC --> CGC (His --> Arg) mutation. The same was the case when cDNA was sequenced, indicating that a beta-Costa Rica-mRNA could not be detected with this procedure. Gene mapping of genomic DNA with Bg/II, BamHI, and HindIII gave normal fragments only and with the same intensity as observed for the fragments of a normal control. The quantities of the beta chain variants Hb J-Iran and Hb Fukuyama with related mutations at beta 77 vary between 30% and 45% in heterozygotes, whereas that of Hb F-Kennestone with the same His --> Arg mutation but in the G gamma-globin gene, is a high 40%-45% (as percentage of total G gamma) in a heterozygous newborn. These different observations exclude a heterozygosity of the A --> G mutation at codon beta 77, as well as a deletion comparable to that of Hbs Lepore or Kenya, or a beta-globin gene duplication, and point to a nontraditional inheritance of Hb Costa Rica. Allele-specific amplification of cDNA with appropriate primers identified the presence of a low level of mutated mRNA in the reticulocytes of the patient, which was confirmed by dotblot analysis of the same material with 32P-labeled probes. Comparable amplification products were not observed in genomic DNA. The A --> G mutation apparently occurred in a somatic cell at a relatively early stage in the development of the hematopoietic cell system, and Hb Costa Rica accumulated through rapid cell divisions in patchy areas in the bone marrow (somatic mosaicism). An unequal distribution of Hb Costa Rica over the red cells supports this possibility.

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Year:  1996        PMID: 8641705

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  29 in total

Review 1.  Nontraditional inheritance.

Authors:  K D Austin; J G Hall
Journal:  Pediatr Clin North Am       Date:  1992-04       Impact factor: 3.278

Review 2.  Review and hypotheses: somatic mosaicism: observations related to clinical genetics.

Authors:  J G Hall
Journal:  Am J Hum Genet       Date:  1988-10       Impact factor: 11.025

3.  High-performance liquid chromatographic separation of human haemoglobins. Simultaneous quantitation of foetal and glycated haemoglobins.

Authors:  E Bisse; H Wieland
Journal:  J Chromatogr       Date:  1988-12-29

4.  Hb Fukuyama [beta 77(EF1)His----Tyr]: a new abnormal hemoglobin discovered in a Japanese.

Authors:  K Hidaka; I Iuchi; K Miyake; H Nakahara; G Iwakawa
Journal:  Hemoglobin       Date:  1988       Impact factor: 0.849

5.  Separation of tryptic peptides of normal and abnormal alpha, beta, gamma, and delta hemoglobin chains by high-performance liquid chromatography.

Authors:  J B Wilson; H Lam; P Pravatmuang; T H Huisman
Journal:  J Chromatogr       Date:  1979-11-21

6.  Allele-specific amplification for the identification of several hemoglobin variants.

Authors:  T P Molchanova; T H Huisman
Journal:  Hemoglobin       Date:  1993-10       Impact factor: 0.849

7.  Detection of common deletional alpha-thalassemia-2 determinants by PCR.

Authors:  E Baysal; T H Huisman
Journal:  Am J Hematol       Date:  1994-07       Impact factor: 10.047

8.  A second, elongated, alpha 2-globin mRNA is present in reticulocytes from normal persons and subjects with terminating codon or poly A mutations.

Authors:  T P Molchanova; N S Smetanina; T H Huisman
Journal:  Biochem Biophys Res Commun       Date:  1995-09-25       Impact factor: 3.575

9.  Heterozygosity for the IVS-I-5 (G-->C) mutation with a G-->A change at codon 18 (Val-->Met; Hb Baden) in cis and a T-->G mutation at codon 126 (Val-->Gly; Hb Dhonburi) in trans resulting in a thalassemia intermedia.

Authors:  V Divoky; E Bissé; J B Wilson; L H Gu; H Wieland; I Heinrichs; J F Prior; T H Huisman
Journal:  Biochim Biophys Acta       Date:  1992-12-10

10.  Clinical and genetic heterogeneity in black patients with homozygous beta-thalassemia from the southeastern United States.

Authors:  J M Gonzalez-Redondo; T A Stoming; K D Lanclos; Y C Gu; A Kutlar; F Kutlar; T Nakatsuji; B Deng; I S Han; V C McKie
Journal:  Blood       Date:  1988-09       Impact factor: 22.113

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  1 in total

1.  Permanence or change? The meaning of genetic variation.

Authors:  F M Salzano
Journal:  Proc Natl Acad Sci U S A       Date:  2000-05-09       Impact factor: 11.205

  1 in total

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