X-chromosome-located microRNAs in immunity: Might they explain male/female differences? The X chromosome-genomic context may affect X-located miRNAs and downstream signaling, thereby contributing to the enhanced immune response of females

被引:201
作者
Pinheiro, Iris [1 ,2 ]
Dejager, Lien [1 ,2 ]
Libert, Claude [1 ,2 ]
机构
[1] Univ Ghent VIB, Dept Mol Biomed Res, B-9052 Ghent, Belgium
[2] Univ Ghent, Dept Biomed Mol Biol, B-9000 Ghent, Belgium
关键词
cancer; genomic context; immunity; miRNAs; X chromosome; INDUCED LEUCINE-ZIPPER; CELLULAR MOSAICISM; TUMOR-SUPPRESSOR; RAPID EVOLUTION; SEX-DIFFERENCES; LINKED GENES; GENDER; INACTIVATION; CANCER; INFLAMMATION;
D O I
10.1002/bies.201100047
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this paper, we hypothesize that X chromosome-associated mechanisms, which affect X-linked genes and are behind the immunological advantage of females, may also affect X-linked microRNAs. The human X chromosome contains 10% of all microRNAs detected so far in the human genome. Although the role of most of them has not yet been described, several X chromosome-located microRNAs have important functions in immunity and cancer. We therefore provide a detailed map of all described microRNAs located on human and mouse X chromosomes, and highlight the ones involved in immune functions and oncogenesis. The unique mode of inheritance of the X chromosome is ultimately the cause of the immune disadvantage of males and the enhanced survival of females following immunological challenges. How these aspects influence X-linked microRNAs will be a challenge for researchers in the coming years, not only from an evolutionary point of view, but also from the perspective of disease etiology.
引用
收藏
页码:791 / 802
页数:12
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