Literature DB >> 1060068

Imbalanced globin chain synthesis in heterozygous beta-thalassemic bone marrow.

G Chalevelakis, J B Clegg, D J Weatherall.   

Abstract

Globin synthesis was studied in the bone marrow of seven heterozygous beta-thalassemic subjects. We found evidence of significant imbalance of alpha- and beta-chain production particularly at short times of incubation. There was a progressive decrease in alpha/beta-chain production ratio with increasing incubation time which was due to a decreased rate of net alpha-chain production, indicating that a large proportion of the newly synthesized alpha chains are degraded, particularly in bone marrow, within a few minutes of synthesis, leading to relatively low alpha/beta ratios if these are measured solely at incubation times greater than 10 min. The significant degradation of excess alpha chains explains why inclusion body formation and ineffective erythropoiesis, notable in beta-thalassemia homozygotes where there is gross chain imbalance, are not observed to any marked degree in heterozygotes.

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Year:  1975        PMID: 1060068      PMCID: PMC433094          DOI: 10.1073/pnas.72.10.3853

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  17 in total

Review 1.  Thalassemia.

Authors:  D G Nathan
Journal:  N Engl J Med       Date:  1972-03-16       Impact factor: 91.245

Review 2.  The clinical and chemical heterogeneity of the beta-thalassemias.

Authors:  D J Weatherall; J B Clegg; A V Roberts; H H Knox-Macaulay
Journal:  Ann N Y Acad Sci       Date:  1974       Impact factor: 5.691

3.  The pattern of hemoglobin precipitation in thalassemia and its significance.

Authors:  X Yataganas; P Fessas
Journal:  Ann N Y Acad Sci       Date:  1969-11-20       Impact factor: 5.691

4.  Regulation of hemoglobin synthesis in beta-thalassemia.

Authors:  E Schwartz; F M Gill
Journal:  Ann N Y Acad Sci       Date:  1974       Impact factor: 5.691

5.  Haemoglobin synthesis during erythroid maturation in -thalassaemia.

Authors:  J B Clegg; D J Weatherall
Journal:  Nat New Biol       Date:  1972-12-06

6.  Compensation of chain synthesis by the single chain gene in Hb Lepore trait.

Authors:  J M White; A Lang; H Lehmann
Journal:  Nat New Biol       Date:  1972-12-27

7.  Decreased beta globin mRNA activity in bone marrow cells in homozygous and heterozygous beta thalassaemia.

Authors:  C Natta; J Banks; G Niazi; P A Marks; A Bank
Journal:  Nat New Biol       Date:  1973-08-29

8.  Abnormal human haemoglobins. Separation and characterization of the alpha and beta chains by chromatography, and the determination of two new variants, hb Chesapeak and hb J (Bangkok).

Authors:  J B Clegg; M A Naughton; D J Weatherball
Journal:  J Mol Biol       Date:  1966-08       Impact factor: 5.469

9.  Synthesis of globin chains in sickle -thalassemia.

Authors:  F M Gill; E Schwartz
Journal:  J Clin Invest       Date:  1973-03       Impact factor: 14.808

10.  Hemoglobin messenger RNA from human bone marrow. Isolation and translation in homozygous and heterozygous beta-thalassemia.

Authors:  A W Nienhuis; P H Canfield; W F Anderson
Journal:  J Clin Invest       Date:  1973-07       Impact factor: 14.808

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  17 in total

Review 1.  Protein quality control during erythropoiesis and hemoglobin synthesis.

Authors:  Eugene Khandros; Mitchell J Weiss
Journal:  Hematol Oncol Clin North Am       Date:  2010-12       Impact factor: 3.722

2.  Trimodality in the proportion of hemoglobin G Philadelphia in heterozygotes: evidence for heterogeneity in the number of human alpha chain loci.

Authors:  R M Baine; D L Rucknagel; P A Dublin; J G Adams
Journal:  Proc Natl Acad Sci U S A       Date:  1976-10       Impact factor: 11.205

3.  Stimulation of fetal hemoglobin synthesis in bone marrow cultures from adult individuals.

Authors:  T H Papayannopoulou; M Brice; G Stamatoyannopoulos
Journal:  Proc Natl Acad Sci U S A       Date:  1976-06       Impact factor: 11.205

4.  Immunological detection of hemoglobin in bones of ancient Roman times and of Iron and Eneolithic Ages.

Authors:  A Ascenzi; M Brunori; G Citro; R Zito
Journal:  Proc Natl Acad Sci U S A       Date:  1985-11       Impact factor: 11.205

5.  Molecular basis of ornithine transcarbamylase deficiency lacking enzyme protein.

Authors:  T Saheki; Y Imamura; I Inoue; S Miura; M Mori; A Ohtake; M Tatibana; N Katsumata; T Ohno
Journal:  J Inherit Metab Dis       Date:  1984       Impact factor: 4.982

6.  Globin chain synthesis in sickle beta-thalassaemic bone marrow and reticulocytes.

Authors:  S Ladas; G Chalevelakis; C Lyberatos; E Vaidakis; G Arapakis
Journal:  J Med Genet       Date:  1979-08       Impact factor: 6.318

7.  Genetic and biosynthetic studies of families carrying hemoglobin J alpha Mexico: association of alpha-thalassemia with HbJ.

Authors:  G Trabuchet; M Benabadji; D Labie
Journal:  Hum Genet       Date:  1978-06-09       Impact factor: 4.132

8.  Analysis of β/α globin ratio by using relative qRT-PCR for diagnosis of beta-thalassemia carriers.

Authors:  Reza Ranjbaran; Mohammad Ali Okhovat; Arash Mobarhanfard; Farzaneh Aboualizadeh; Mozhdeh Abbasi; Leili Moezzi; Habib Allah Golafshan; Abbas Behzad-Behbahani; Mandana Bagheri; Sedigheh Sharifzadeh
Journal:  J Clin Lab Anal       Date:  2013-07       Impact factor: 2.352

9.  Genetics of cat hemoglobins: a quantitative polymorphism.

Authors:  N Spencer
Journal:  Biochem Genet       Date:  1979-08       Impact factor: 1.890

10.  Heterogeneity in beta 0 thalassemia from Algeria: genetic, clinical and molecular studies.

Authors:  M Belhani; F Morlé; P Colonna; J Godet
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

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