The () region comprises a fast-evolving family of genes that encode receptors for natural killer (NK) cells and have crucial role in host defense. Evolution of was examined in the context of the human genome. Gene-content diversity and single nucleotide polymorphisms (SNP) in the genes and flanking regions were compared to >660,000 genome-wide SNPs in over 800 individuals from 52 populations of the human genome diversity panel (HGDP). allelic diversity was further examined using next generation sequencing in a subset of 56 individuals. We identified the SNP located in as a marker of and and, consequently, Cen A and Cen B haplotypes. We also show that combinations of two SNPs ( and ) distinguish from and also define the major high- and low-expressing alleles lineages. Comparing the diversity of the SNPs within the region to remainder of the genome, we observed a high diversity for the centromeric region consistent with balancing selection ( < 0.01); in contrast, centromeric diversity is significantly reduced in East Asian populations ( < 0.01), indicating purifying selection. By analyzing SNP haplotypes in a region spanning ~500 kb that includes the cluster, we observed evidence of strong positive selection in Africa for high-expressing alleles, favored over the low-expressing alleles ( < 0.01). In sharp contrast, the strong positive selection ( < 0.01) that we also observed in the telomeric region in Oceanic populations tracked with a high frequency of . In addition, we demonstrated that worldwide frequency of high-expression alleles was correlated with virus with virus (r = 0.64, < 10) and protozoa (r = 0.69, < 10) loads, which points to selection globally on high-expressing alleles attributable to pathogen exposure.
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http://dx.doi.org/10.3389/fimmu.2019.00989 | DOI Listing |
Medicine (Baltimore)
January 2025
Department of Thoracic Surgery, Renmin Hospital of Wuhan University, Wuhan, China.
While recent studies suggested a potential causal link between type 1 diabetes mellitus (T1DM) but not type 2 diabetes mellitus (T2DM) and idiopathic pulmonary fibrosis (IPF), the involved mechanism remains unclear. Here, using a Mendelian randomization (MR) approach, we verified the causal relationship between the two types of diabetes mellitus and IPF and investigated the possible role of inflammation in the association between diabetes mellitus and IPF. Based on genome-wide association study (GWAS) summary data of T1DM, T2DM, and IPF, the univariable MR, multivariable MR (MVMR), and mediation MR were successively used to analyze the causal relationship.
View Article and Find Full Text PDFMedicine (Baltimore)
January 2025
Renmin Hospital of Wuhan University, Wuhan, Hubei Province, People's Republic of China.
Colorectal cancer (CRC) is one of the most common cancers worldwide and inflammation is believed to play an important role in CRC. In this study, we comprehensively analyzed the causal association between 91 circulating inflammatory cytokines and the risk of CRC using Mendelian randomization (MR). Based on genome-wide association study summary statistics, we examined the causal effects of 91 circulating inflammatory cytokines on CRC.
View Article and Find Full Text PDFMedicine (Baltimore)
January 2025
National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, China.
The correlation between cathepsins and pulmonary arterial hypertension (PAH) is well-established, but the causative link between them remains uncertain. This study aimed to explore the causal role of circulating metabolites mediating cathepsins in PAH using Mendelian randomization (MR). A 2-sample 2-step MR method was used to identify causal relationship between cathepsins and PAH; causal relationship between circulating metabolites and PAH; and mediated effects of these circulating metabolites.
View Article and Find Full Text PDFPLoS Biol
January 2025
School of Life Science and Technology, ShanghaiTech University, Shanghai, China.
The organization of the human genome in space and time is critical for transcriptional regulation and cell fate determination. However, robust methods for tracking genome organization or genomic interactions over time in living cells are lacking. Here, we developed a multicolor DNA labeling system, ParSite, to simultaneously track triple genomic loci in the U2OS cells.
View Article and Find Full Text PDFSci Adv
January 2025
Department of Biostatistics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Genes on the X chromosome are extensively expressed in the human brain. However, little is known for the X chromosome's impact on the brain anatomy, microstructure, and functional networks. We examined 1045 complex brain imaging traits from 38,529 participants in the UK Biobank.
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