Literature DB >> 7745837

[Hb M-Iwate [alpha 87 (F8) His-->Tyr]: analysis of the genomic DNA and biosynthesis].

M Orisaka1, T Sasaki, J Kato, K Harano, T Harano.   

Abstract

Hb M-Iwate [alpha 87 (F8) His-->Tyr] was identified as the cause of cyanosis in a 21-year-old Japanese female. Amplification and sequencing of the alpha 2- and alpha 1-genes demonstrated the mutation CD87 CAC (His)-->TAC (Tyr) in the alpha 2-gene. Analysis of the in vitro globin biosynthesis in the reticulocytes disclosed a well-balanced beta/alpha synthetic ratio of 1.04 but an unexpectedly low alpha M/total alpha. Although the cause of the lowered alpha M-globin biosynthesis is not yet clear, it might be related to a defect in chain assembly rather than to a modified stability or a reduced amount of the abnormal alpha-globin mRNA.

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Year:  1995        PMID: 7745837

Source DB:  PubMed          Journal:  Rinsho Byori        ISSN: 0047-1860


  2 in total

1.  Familial congenital cyanosis caused by Hb-M(Yantai)(α-76 GAC → TAC, Asp → Tyr).

Authors:  Yanbo Sun; Pingyu Wang; Youjie Li; Fei Jiao; Zunling Li; Ying Ma; Wei Li; Shuyang Xie
Journal:  Genet Mol Biol       Date:  2010-09-01       Impact factor: 1.771

2.  De novo alpha 2 hemoglobin gene (HBA2) mutation in a child with hemoglobin M Iwate and symptomatic methemoglobinemia since birth.

Authors:  Marcos Borato Viana; André Rolim Belisário
Journal:  Rev Bras Hematol Hemoter       Date:  2014-03-29
  2 in total

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