We studied 201 unrelated French Basque individuals for HLA and Bf polymorphisms. The haplotypes of eighty-seven of them were deduced from family studies. The results show the frequency of the Bf F1 allele (0.1393) which is the highest one currently reported. They confirm the high frequencies of HLA-Aw19.2 and B18 previously reported in that population and show that a whole haplotype with strong linkage disequilibria, namely Aw19.2, Cw5, B18, Bf F1, DRw3 is frequent. On the other hand, the gene frequency of Bf S is decreased (0.5497) as compared with the other European Caucasoïd populations, while a slight increase in the Bf F gene frequency (0.2960) appears. These results point out that it is of importance to consider the genetic background choosing the population where linkage disequilibria are to be studied.

Download full-text PDF

Source
http://dx.doi.org/10.1111/j.1744-313x.1980.tb00739.xDOI Listing

Publication Analysis

Top Keywords

linkage disequilibria
8
gene frequency
8
high frequency
4
frequency properdin
4
properdin factor
4
factor linkage
4
linkage hla
4
hla french
4
french basques
4
basques studied
4

Similar Publications

Background And Objectives: The Rh blood group system is the most polymorphic human blood group system. Previous studies have investigated variants in the RHD and RHCE promoter. The relevance of these variants to the Chinese Han population is further clarified in this study.

View Article and Find Full Text PDF

Each new human has an expected = 2 - 10 new deleterious mutations. This deluge of deleterious mutations cannot all be purged, and therefore accumulate in a declining fitness ratchet. Using a novel simulation framework designed to efficiently handle genome-wide linkage disequilibria across many segregating sites, we find that rarer, beneficial mutations of larger effect are sufficient to compensate fitness declines due to the fixation of many slightly deleterious mutations.

View Article and Find Full Text PDF
Article Synopsis
  • This paper examines how polygenic adaptation and reproductive isolation are shaped by linkage disequilibria (LD) in populations undergoing both gene flow and genetic drift.
  • It demonstrates that incorporating effective migration rates into diffusion approximations can accurately predict changes in allele frequencies and heterozygosity at selected and neutral loci, respectively.
  • The study explores conditions for maintaining local adaptation in different environments, revealing how LD can facilitate the elimination of harmful alleles and influence divergence between subpopulations sharing the same habitat.
View Article and Find Full Text PDF

A previous exploratory analysis of a COMT gene single-nucleotide polymorphism (SNP) and a DRD3 SNP by our group suggested possible contributions to pain-related acute care utilization in people with sickle cell disease (SCD). Our aim was to extend the analysis to gene-spanning haplotypes of COMT SNPs and DRD3 SNPs to investigate possible associations with pain intensity and pain-related acute care utilization in an SCD cohort. Genotyping was conducted, and clinical data were collected, including self-reported pain intensity using PAINReportIt (average of current pain and least and worst in past 24 hours, average pain intensity [API]) and medical record-extracted, pain-related acute care utilization data of 130 adults with SCD.

View Article and Find Full Text PDF

Genotype Groups of the Wheat Leaf Rust Fungus in the United States as Determined by Genotyping by Sequencing.

Phytopathology

March 2022

U.S. Department of Agriculture-Agricultural Research Service, Hard Winter Wheat Genetics Research Unit, Manhattan, KS 66506.

Wheat leaf rust caused by is a widespread disease of wheat in the United States and worldwide. Populations of are characterized by virulence phenotypes that change rapidly because of selection by wheat cultivars with leaf rust resistance genes. The objective of this study was to genotype collections of from 2011 to 2018 in the United States using restriction site-associated genotyping by sequencing (GBS) to determine if recently identified new virulence phenotypes belong to established genotype groups or to groups previously not detected.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!