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PMID: 429552 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Further studies of the frequency and significance of the Tgamma-chain of human fetal hemoglobin.

The Journal of clinical investigation ·Vol. 63 ·No. 2 ·1979-02-00 ·Pages 268-75

Schroeder WA, Huisman TH, Efremov GD, Shelton JR, Shelton JB, Phillips R, Reese A, Gravely M, Harrison JM, Lam H

Abstract

A further study of the Tgamma-chain in a variety of conditions has revealed its presence in the cord bloods of ethnic groups previously unstudied. Heterozygous newborn average 17-19% Tgamma-chain while the mean value in four presumed homozygotes was 31%. The Tgamma-chain is readily detectable in beta-thalassemia of various ethnic groups (although infrequent in Blacks) as well as in deltabeta-thalassemia. Studies of a few families have provided an opportunity to determine whether or not certain individuals are heterozygous or homozygous for the Tgamma-gene. The Tgamma-chain has not been detected in the human fetal hemoglobin that is synthesized in increased amounts in persons with the hereditary persistence of fetal hemoglobin. Although the Tgamma-chain is detectable in sickle cell anemia, its frequency appears to be lower than in normal individuals. By focusing upon the relationship of the percentage of Tgamma-chain to the sources of human fetal globulin from determinants in cis and in trans, the conclusion has been reached that the Tgamma-chain is the product of a mutant Agamma-locus which should be named the TAgamma-chain.

MeSH Terms
Adult Anemia, Sickle Cell/blood Chemical Phenomena Chemistry Female Fetal Blood/analysis Fetal Hemoglobin/genetics Hemoglobins, Abnormal Humans Infant, Newborn Male Pedigree Racial Groups Thalassemia/blood,genetics
Chemicals
Hemoglobins, Abnormal Fetal Hemoglobin
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Schroeder W A
Huisman T H
Efremov G D
Shelton J R
Shelton J B
Phillips R
Reese A
Gravely M
Harrison J M
Lam H
References (20)
20 references, click to expand
  1. Demonstration of two alpha-globin genes per human haploid genome for normals and Hb J Mexico.
    Eur J Biochem. 1977 Aug 15;78(1):161-5 PMID: 71990
  2. The V gamma chain of fetal hemoglobin of the orangutan.
    Biochem Genet. 1978 Dec;16(11-12):1203-5 PMID: 751647
  3. The T gamma chain of human fetal hemoglobin at birth and in several abnormal hematologic conditions.
    Pediatr Res. 1977 Oct;11(10 Pt 2):1102-5 PMID: 904975
  4. Haemoglobin F Melbourne Ggamma 16 Gly leads to Arg and haemoglobin F carlton Ggamma 121 Glu leads to Lys. Further evidence for varied activity of gamma-chain genes.
    Biochim Biophys Acta. 1977 Feb 22;490(2):452-5 PMID: 836882
  5. Anomaly in the gamma chain heterogeneity of the newborn.
    Nature. 1977 Jan 6;265(5589):63-5 PMID: 834242
  6. Globin synthesis in the Jamaican Negro with beta-thalassaemia.
    Br J Haematol. 1974 Dec;28(4):505-13 PMID: 4455302
  7. The present status of the heterogeneity of fetal hemoglobin in beta-thalassemia: an attempt to unify some observations in thalassemia and related conditions.
    Ann N Y Acad Sci. 1974;232(0):107-24 PMID: 4528800
  8. Non-synchronized suppression of postnatal activity in non-allelic genes which synthesize the Ggamma chain in human foetal haemoglobin.
    Nat New Biol. 1973 Jul 18;244(133):89-90 PMID: 4516146
  9. A direct estimate of the number of human gamma-globin genes.
    Cell. 1976 May;8(1):13-8 PMID: 954089
  10. Search for nonallelic structural genes for gamma-chains of fetal hemoglobin in some primates.
    Biochem Genet. 1973 Nov;10(3):309-18 PMID: 4201857
  11. Hemoglobin Kenya, the product of a gamma-beta fusion gene: studies of the family.
    Am J Hum Genet. 1973 Sep;25(5):548-63 PMID: 4741849
  12. A homozygote for the Hb G type of foetal haemoglobin in India: a study of two Indian and four Negro families.
    Br J Haematol. 1972 Oct;23(4):403-17 PMID: 5084806
  13. Evidence for four nonallelic structural genes for the chain of human fetal hemoglobin.
    Biochem Genet. 1972 Oct;7(2):131-9 PMID: 5050916
  14. A new Hb variant: Hb F Sardinia gamma75(E19) isoleucine leads to threonine found in a family with Hb G Philadelphia, beta-chain deficiency and a Lepore-like haemoglobin indistinguishable from Hb A2.
    Acta Haematol. 1975;53(6):347-55 PMID: 808940
  15. Significance of a new type of human fetal hemoglobin carrying a replacement isoleucine replaced by threonine at position 75 )E 19) of the gamma chain.
    Hum Genet. 1976 Jun 29;32(3):305-13 PMID: 939551
  16. Delta Beta-Thalassaemia in two yugoslavian families.
    Scand J Haematol. 1975 May;14(3):226-32 PMID: 1145125
  17. Evidence for multiple structural genes for the gamma chain of human fetal hemoglobin.
    Proc Natl Acad Sci U S A. 1968 Jun;60(2):537-44 PMID: 5248810
  18. Evidence for multiple structural genes for the gamma-chain of human fetal hemoglobin in hereditary persistence of fetal hemoglobin.
    Ann N Y Acad Sci. 1969 Nov 20;165(1):320-31 PMID: 5260154
  19. Nature of fetal hemoglobin in the Greek type of hereditary persistence of fetal hemoglobin with and without concurrent beta-thalassemia.
    J Clin Invest. 1970 May;49(5):1035-40 PMID: 5441539
  20. A possible subclass of the hereditary persistence of fetal hemoglobin.
    Blood. 1970 Jul;36(1):1-9 PMID: 5421741
Article Info
Journal
The Journal of clinical investigation
Abbr.
J Clin Invest
ISSN
0021-9738
Published
1979-02-00
Pages
268-75
Language
English
Region
United States
NLM ID
7802877
PMCID
PMC371949
Subset
IM
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