Literature DB >> 1376298

A novel sickle cell mutation of yet another origin in Africa: the Cameroon type.

C Lapouméroulie1, O Dunda, R Ducrocq, G Trabuchet, M Mony-Lobé, J M Bodo, P Carnevale, D Labie, J Elion, R Krishnamoorthy.   

Abstract

The sickle cell mutation (beta s) arose as at least three independent events in Africa and once in Asia, being termed the Senegal, Benin, Bantu and Indian types respectively. An investigation in Cameroon was carried out to determine whether the atypical sickle genes observed in the neighboring countries are the result of recombination or the presence of a sickle cell mutation of a different genetic origin. It was conducted on 40 homozygous SS patients followed at the Blood Transfusion Center in the capital city of Yaoundé. On 80 beta s chromosomes, 13 exhibited a novel polymorphic pattern that was observed three times in the homozygous state. This chromosome contains an A gamma T gene. The restriction fragment length polymorphism haplotype is different from all the other beta s chromosomes in both the 5' and 3' regions, but has previously been reported in sporadic cases. The (AT)8(T)5 sequence in the -500 region of the beta gene is specific and different from that of the Senegal, Benin, Bantu or Indian beta s genes. All the carriers of this specific chromosome belong to the Eton ethnic group and originate from the Sanaga river valley. This observation strongly argues for yet another independent origin of the sickle cell mutation in Africa, here referred to as the "Cameroon type". The Benin haplotype and a Benin/Bantu recombinant haplotype have been observed in the other studied populations: Ewondo, Bamiléké, Bassa, Yambassa and Boulou.

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Year:  1992        PMID: 1376298     DOI: 10.1007/bf00220553

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


  25 in total

1.  The hematologic characteristics of sickle cell anemia bearing the Bantu haplotype: the relationship between G gamma and HbF level.

Authors:  R L Nagel; S K Rao; O Dunda-Belkhodja; M M Connolly; M E Fabry; A Georges; R Krishnamoorthy; D Labie
Journal:  Blood       Date:  1987-04       Impact factor: 22.113

2.  Haplotypes in tribal Indians bearing the sickle gene: evidence for the unicentric origin of the beta S mutation and the unicentric origin of the tribal populations of India.

Authors:  D Labie; R Srinivas; O Dunda; C Dode; C Lapoumeroulie; V Devi; S Devi; K Ramasami; J Elion; R Ducrocq
Journal:  Hum Biol       Date:  1989-08       Impact factor: 0.553

3.  Polymerase chain reaction amplification applied to the determination of beta-like globin gene cluster haplotypes.

Authors:  M Sutton; E E Bouhassira; R L Nagel
Journal:  Am J Hematol       Date:  1989-09       Impact factor: 10.047

4.  Generation of single-stranded DNA by the polymerase chain reaction and its application to direct sequencing of the HLA-DQA locus.

Authors:  U B Gyllensten; H A Erlich
Journal:  Proc Natl Acad Sci U S A       Date:  1988-10       Impact factor: 11.205

5.  Geographical survey of beta S-globin gene haplotypes: evidence for an independent Asian origin of the sickle-cell mutation.

Authors:  A E Kulozik; J S Wainscoat; G R Serjeant; B C Kar; B Al-Awamy; G J Essan; A G Falusi; S K Haque; A M Hilali; S Kate
Journal:  Am J Hum Genet       Date:  1986-08       Impact factor: 11.025

6.  Multiple origins of the sickle mutation: evidence from beta S globin gene cluster polymorphisms.

Authors:  J S Wainscoat; J I Bell; S L Thein; D R Higgs; G R Sarjeant; T E Peto; D J Weatherall
Journal:  Mol Biol Med       Date:  1983-09

Review 7.  DNA polymorphism and molecular pathology of the human globin gene clusters.

Authors:  S E Antonarakis; H H Kazazian; S H Orkin
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

8.  Evidence for the multicentric origin of the sickle cell hemoglobin gene in Africa.

Authors:  J Pagnier; J G Mears; O Dunda-Belkhodja; K E Schaefer-Rego; C Beldjord; R L Nagel; D Labie
Journal:  Proc Natl Acad Sci U S A       Date:  1984-03       Impact factor: 11.205

9.  Origin of the beta S-globin gene in blacks: the contribution of recurrent mutation or gene conversion or both.

Authors:  S E Antonarakis; C D Boehm; G R Serjeant; C E Theisen; G J Dover; H H Kazazian
Journal:  Proc Natl Acad Sci U S A       Date:  1984-02       Impact factor: 11.205

10.  Structural analysis of the 5' flanking region of the beta-globin gene in African sickle cell anemia patients: further evidence for three origins of the sickle cell mutation in Africa.

Authors:  Y Chebloune; J Pagnier; G Trabuchet; C Faure; G Verdier; D Labie; V Nigon
Journal:  Proc Natl Acad Sci U S A       Date:  1988-06       Impact factor: 11.205

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  39 in total

1.  Molecular analysis of the beta-globin gene cluster in the Niokholo Mandenka population reveals a recent origin of the beta(S) Senegal mutation.

Authors:  Mathias Currat; Guy Trabuchet; David Rees; Pascale Perrin; Rosalind M Harding; John B Clegg; André Langaney; Laurent Excoffier
Journal:  Am J Hum Genet       Date:  2001-12-06       Impact factor: 11.025

2.  Analysis of the 5' flanking sequence of the G gamma globin gene by denaturing gradient gel electrophoresis confirms the heterogeneity of the Bantu beta S haplotype.

Authors:  G Tachdjian; M Benabdennebi; C Guidal; C Sayada; C Lapouméroulie; J Elion
Journal:  Hum Genet       Date:  1992 Sep-Oct       Impact factor: 4.132

3.  Two lessons from the interface of genetics and medicine.

Authors:  Anthony C Allison
Journal:  Genetics       Date:  2004-04       Impact factor: 4.562

Review 4.  Genetic modifiers of sickle cell disease.

Authors:  Martin H Steinberg; Paola Sebastiani
Journal:  Am J Hematol       Date:  2012-05-28       Impact factor: 10.047

Review 5.  Fetal hemoglobin in sickle cell anemia.

Authors:  Idowu Akinsheye; Abdulrahman Alsultan; Nadia Solovieff; Duyen Ngo; Clinton T Baldwin; Paola Sebastiani; David H K Chui; Martin H Steinberg
Journal:  Blood       Date:  2011-04-13       Impact factor: 22.113

6.  Oculocutaneous albinism type 2 (OCA2) with homozygous 2.7-kb deletion of the P gene and sickle cell disease in a Cameroonian family. Identification of a common TAG haplotype in the mutated P gene.

Authors:  Robert Aquaron; Nadem Soufir; Jean-Louis Bergé-Lefranc; Catherine Badens; Frederic Austerlitz; Bernard Grandchamp
Journal:  J Hum Genet       Date:  2007-09-01       Impact factor: 3.172

7.  Abnormal hemoglobins among Kurdish population of Western Iran: hematological and molecular features.

Authors:  Zohreh Rahimi; Adriana Muniz; Hadi Mozafari
Journal:  Mol Biol Rep       Date:  2009-03-31       Impact factor: 2.316

8.  Echocardiographic evaluation of left ventricular diastolic and systolic function in Saudi patients with sickle cell disease.

Authors:  Mohammed Fakhry Abdul-Mohsen
Journal:  J Saudi Heart Assoc       Date:  2012-06-12

9.  Biological impact of α genes, β haplotypes, and G6PD activity in sickle cell anemia at baseline and with hydroxyurea.

Authors:  Françoise Bernaudin; Cécile Arnaud; Annie Kamdem; Isabelle Hau; Françoise Lelong; Ralph Epaud; Corinne Pondarré; Serge Pissard
Journal:  Blood Adv       Date:  2018-03-27

10.  Self-catalytic DNA depurination underlies human β-globin gene mutations at codon 6 that cause anemias and thalassemias.

Authors:  Juan R Alvarez-Dominguez; Olga Amosova; Jacques R Fresco
Journal:  J Biol Chem       Date:  2013-03-01       Impact factor: 5.157

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