The Ashkenazic Jewish bloom syndrome mutation blm(Ash) is present in non-Jewish Americans of Spanish ancestry

Citation
Na. Ellis et al., The Ashkenazic Jewish bloom syndrome mutation blm(Ash) is present in non-Jewish Americans of Spanish ancestry, AM J HU GEN, 63(6), 1998, pp. 1685-1693
Citations number
18
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Molecular Biology & Genetics
Journal title
AMERICAN JOURNAL OF HUMAN GENETICS
ISSN journal
00029297 → ACNP
Volume
63
Issue
6
Year of publication
1998
Pages
1685 - 1693
Database
ISI
SICI code
0002-9297(199812)63:6<1685:TAJBSM>2.0.ZU;2-L
Abstract
Bloom syndrome (BS) is more frequent in the Ashkenazic Jewish population th an in any other. There. the predominant mutation, referred to as "blm(Ash), " is a 6-bp deletion and 7-bp insertion at nucleotide position 2281 in the BLM cDNA. Using a convenient PCR assay, we have identified blm(Ash) on 58 o f 60 chromosomes transmitted by Ashkenazic parents to persons with BS. In c ontrast, in 91 unrelated non-Ashkenazic persons with BS whom we examined, b lm(Ash) was identified only in 5, these, coming from Spanish-speaking Chris tian families from the southwestern United States, Mexico, or El Salvador. These data, along with haplotype analyses, show that blm(Ash) was independe ntly established through a founder effect in Ashkenazic Jews and in immigra nts to formerly Spanish colonies. This striking observation underscores the complexity of Jewish history and demonstrates the importance of migration and genetic drift in the formation of human populations.