Literature DB >> 10629573

Atypical beta(s) haplotypes are generated by diverse genetic mechanisms.

M A Zago1, W A Silva, B Dalle, S Gualandro, M H Hutz, C Lapoumeroulie, M H Tavella, A G Araujo, J E Krieger, J Elion, R Krishnamoorthy.   

Abstract

The majority of the chromosomes with the beta(S) gene have one of the five common haplotypes, designated as Benin, Bantu, Senegal, Cameroon, and Arab-Indian haplotypes. However, in every large series of sickle cell patients, 5-10% of the chromosomes have less common haplotypes, usually referred to as "atypical" haplotypes. In order to explore the genetic mechanisms that could generate these atypical haplotypes, we extended our analysis to other rarely studied polymorphic markers of the beta(S)-gene cluster, in a total of 40 chromosomes with uncommon haplotypes from Brazil and Cameroon. The following polymorphisms were examined: seven restriction site polymorphisms of the epsilongammadeltabeta-cluster, the pre-(G)gamma framework sequence including the 6-bp deletion/insertion pattern, HS-2 LCR (AT)xR(AT)y and pre-beta (AT)xTy repeat motifs, the GC/TT polymorphism at -1105-1106 of (G)gamma-globin gene, the C/T polymorphism at -551 of the beta-globin gene, and the intragenic beta-globin gene framework. Among the Brazilian subjects, the most common atypical structure (7/16) was a Bantu 3'-subhaplotype associated with different 5'-sequences, while in two chromosomes a Benin 3'-subhaplotype was associated with two different 5'-subhaplotypes. A hybrid Benin/Bantu configuration was also observed. In three chromosomes, the atypical haplotype differed from the typical one by the change of a single restriction site. In 2/134 chromosomes identified as having a typical Bantu RFLP-haplotype, a discrepant LCR repeat sequence was observed, probably owing to a crossover 5' to the epsilon-gene. Among 80 beta(S) chromosomes from Cameroon, 22 were associated with an atypical haplotype. The most common structure was represented by a Benin haplotype (from the LCR to the beta-gene) with a non-Benin segment 3' to the beta-globin gene. In two cases a Bantu LCR was associated with a Benin haplotype and a non-Benin segment 3' to the beta-globin gene. In three other cases, a more complex structure was observed that can be considered as a hybrid of Benin, Bantu, Senegal, or other chromosomes was observed. These data suggest that the atypical beta(S) haplotypes are not uncommon in America and in Africa. These haplotypes are probably generated by a variety of genetic mechanisms including (a) isolated nucleotide changes in one of the polymorphic restriction sites, (b) simple and double crossovers between two typical beta(S) haplotypes or much more frequently between a typical beta(S) haplotype and a different beta(A)-associated haplotype that was present in the population, and (c) gene conversions. Copyright 2000 Wiley-Liss, Inc.

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Year:  2000        PMID: 10629573     DOI: 10.1002/(sici)1096-8652(200002)63:2<79::aid-ajh4>3.0.co;2-d

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  11 in total

1.  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

Review 2.  Beta-globin gene haplotypes among cameroonians and review of the global distribution: is there a case for a single sickle mutation origin in Africa?

Authors:  Valentina J Ngo Bitoungui; Gift D Pule; Neil Hanchard; Jeanne Ngogang; Ambroise Wonkam
Journal:  OMICS       Date:  2015-03

3.  Fetal Hemoglobin in Tunisian Sickle Cell Disease Patient: Relationship with Polymorphic Sequences Cis to the β-Globin Gene.

Authors:  Imen Moumni; Maha Ben Mustapha; Ikbel Ben Mansour; Amine Zoraï; Kaïs Douzi; Sarah Sassi; Dorra Chaouachi; Fethi Mellouli; Mohamed Bejaoui; Salem Abbes
Journal:  Indian J Hematol Blood Transfus       Date:  2015-01-23       Impact factor: 0.900

4.  Sickle cell anemia: clinical diversity and beta S-globin haplotypes.

Authors:  Sandra Regina Loggetto
Journal:  Rev Bras Hematol Hemoter       Date:  2013

Review 5.  An Expert Review of Pharmacogenomics of Sickle Cell Disease Therapeutics: Not Yet Ready for Global Precision Medicine.

Authors:  Khuthala Mnika; Gift D Pule; Collet Dandara; Ambroise Wonkam
Journal:  OMICS       Date:  2016-09-16

6.  Determination of β haplotypes in patients with sickle-cell anemia in the state of Rio Grande do Norte, Brazil.

Authors:  Cynthia Hatsue Kitayama Cabral; Edvis Santos Soares Serafim; Waleska Rayane Dantas Bezerra de Medeiros; Thales Allyrio Araújo de Medeiros Fernandes; Elza Miyuki Kimura; Fernando Ferreira Costa; Maria de Fátima Sonati; Ivanise Marina Moretti Rebecchi; Tereza Maria Dantas de Medeiros
Journal:  Genet Mol Biol       Date:  2011-07-01       Impact factor: 1.771

7.  Frequency and origin of haplotypes associated with the beta-globin gene cluster in individuals with trait and sickle cell anemia in the Atlantic and Pacific coastal regions of Colombia.

Authors:  Cristian Fong; María Alejandra Lizarralde-Iragorri; Diana Rojas-Gallardo; Guillermo Barreto
Journal:  Genet Mol Biol       Date:  2013-11-08       Impact factor: 1.771

8.  The effects of old and recent migration waves in the distribution of HBB*S globin gene haplotypes.

Authors:  Juliana D Lindenau; Sandrine C Wagner; Simone M de Castro; Mara H Hutz
Journal:  Genet Mol Biol       Date:  2016-10-03       Impact factor: 1.771

9.  Molecular Analysis of Xmn1-Polymorphic Site ´5 to Gγ of the β-Globin Gene Cluster in a Saudi Population of Jazan Region in Correlation with Hb F Expression.

Authors:  Abozer Y Elderdery; Abdullah Alsrhani; Badr Alzahrani; Muhammad Atif; Ahmed I Refaiy; Hussain Shiwani; Amin Abbas; Dawelbiet A Yahia
Journal:  Evid Based Complement Alternat Med       Date:  2022-03-21       Impact factor: 2.629

10.  Molecular analysis and association with clinical and laboratory manifestations in children with sickle cell anemia.

Authors:  Roberta Faria Camilo-Araújo; Olga Maria Silverio Amancio; Maria Stella Figueiredo; Ana Carolina Cabanãs-Pedro; Josefina Aparecida Pellegrini Braga
Journal:  Rev Bras Hematol Hemoter       Date:  2014-07-09
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