Literature DB >> 22834944

PTX3 genetic variation and dizygotic twinning in the Gambia: could pleiotropy with innate immunity explain common dizygotic twinning in Africa?

Giorgio Sirugo1, Digna R Velez Edwards, Kelli K Ryckman, Cyrille Bisseye, Marquitta J White, Bunja Kebbeh, Gerard A J Morris, Richard A Adegbola, Alessandra Tacconelli, Irene M Predazzi, Giuseppe Novelli, Fredrik O Vannberg, Kunle Odunsi, Grier P Page, Scott M Williams.   

Abstract

Dizygotic (DZ) twinning has a genetic component and is common among sub-Saharan Africans; in The Gambia its frequency is up to 3% of live births. Variation in PTX3, encoding Pentraxin 3, a soluble pattern recognition receptor that plays an important role both in innate immunity and in female fertility, has been associated with resistance to Mycobacterium tuberculosis pulmonary disease and to Pseudomonas aeruginosa infection in cystic fibrosis patients. We tested whether PTX3 variants in Gambian women associate with DZ twinning, by genotyping five PTX3 single nucleotide polymorphisms (SNPs) in 130 sister pairs (96 full sibs and 34 half sibs) who had DZ twins. Two, three and five SNP haplotypes differed in frequency between twinning mothers and those without a history of twinning (from P = 0.006 to 3.03e-06 for two SNP and three SNP haplotypes, respectively). Twinning mothers and West African tuberculosis-controls from a previous study shared several frequent haplotypes. Most importantly, our data are consistent with an independently reported association of PTX3 and female fertility in a sample from Ghana. Taken together, these results indicate that selective pressure on PTX3 variants that affect the innate immune response to infectious agents, could also produce the observed high incidence of DZ twinning in Gambians.
© 2012 The Authors Annals of Human Genetics © 2012 Blackwell Publishing Ltd/University College London.

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Year:  2012        PMID: 22834944      PMCID: PMC3731069          DOI: 10.1111/j.1469-1809.2012.00723.x

Source DB:  PubMed          Journal:  Ann Hum Genet        ISSN: 0003-4800            Impact factor:   1.670


  36 in total

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