The compleX balancing act of controlling X-chromosome dosage and how it impacts mammalian germline development

被引:5
作者
Mattimoe, Tom [1 ]
Payer, Bernhard [1 ,2 ]
机构
[1] Barcelona Inst Sci & Technol, Ctr Genom Regulat CRG, Carrer Dr Aiguader 88, Barcelona 08003, Spain
[2] Univ Pompeu Fabra UPF, Barcelona, Spain
关键词
LONG NONCODING RNA; CELL-LIKE CELLS; UP-REGULATION; GENE-EXPRESSION; DNA METHYLATION; EARLY EMBRYOS; LINKED GENES; MOUSE EMBRYO; FEMALE MICE; HISTONE H4;
D O I
10.1042/BCJ20220450
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 female mammals, the two X chromosomes are subject to epigenetic gene regulation in order to balance X-linked gene dosage with autosomes and in relation to males, which have one X and one Y chromosome. This is achieved by an intricate interplay of several processes; X-chromosome inactivation and reactivation elicit global epigenetic regulation of expression from one X chromosome in a stage-specific manner, whilst the process of X-chromosome upregulation responds to this by fine-tuning transcription levels of the second X. The germline is unique in its function of transmitting both the genetic and epigenetic information from one generation to the next, and remodelling of the X chromosome is one of the key steps in setting the stage for successful development. Here, we provide an overview of the complex dynamics of X-chromosome dosage control during embryonic and germ cell development, and aim to decipher its potential role for normal germline competency.
引用
收藏
页码:521 / 537
页数:17
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