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Transmission ratio distortion (TRD) describes a significant departure from expected Mendelian inheritance ratios that is fundamental to both the biology of reproduction and statistical genetics. The relatively high fetal wastage in humans, with consequent selection of alleles in utero, makes it likely that TRD is prevalent in the human genome. The central region of the human major histocompatibility complex (MHC) is a strong TRD candidate, as it houses a number of immune and regulatory genes that may be important in pregnancy outcome. We used a nonhaplotype-based method to select 13 tagging SNPs from three central MHC candidate regions, and analysed their transmission in 380 newborns and their parents (1138 individuals). A TRD of 54:46 was noted in favour of the common allele of a promoter SNP in the CLIC1 gene (P = 0.025), with a similar distortion using haplotypes across the same gene region (P = 0.016). We also found evidence that markers in the CLIC1 gene region may have been subject to recent selection (P < 0.001). The study illustrates the potential benefits of screening for TRD and highlights the difficulties encountered therein.

Original publication

DOI

10.1038/sj.gene.6364277

Type

Journal article

Journal

Genes Immun

Publication Date

01/2006

Volume

7

Pages

51 - 58

Keywords

Biomarkers, Female, Haplotypes, Homeodomain Proteins, Humans, Lymphotoxin-alpha, Major Histocompatibility Complex, Male, Polymorphism, Single Nucleotide, Pregnancy, Prospective Studies, Proto-Oncogene Proteins, Receptor, Notch4, Receptors, Notch, Tumor Necrosis Factor-alpha