Mouse primordial germ-cell-like cells lack piRNAs

被引:1
作者
Ramakrishna, Navin B. [1 ,2 ,3 ,7 ]
Battistoni, Giorgia [4 ]
Surani, M. Azim [1 ,3 ,5 ]
Hannon, Gregory J. [4 ]
Miska, Eric A. [1 ,2 ,6 ,8 ]
机构
[1] Univ Cambridge, Wellcome CRUK Gurdon Inst, Cambridge CB2 1QN, England
[2] Univ Cambridge, Dept Genet, Cambridge CB2 3EH, England
[3] Univ Cambridge, Dept Physiol Dev & Neurosci, Cambridge CB2 3EL, England
[4] Univ Cambridge, Li Ka Shing Ctr, CRUK Cambridge Inst, Cambridge CB2 0RE, England
[5] Univ Cambridge, Wellcome MRC Cambridge Stem Cell Inst, Cambridge CB2 0AW, England
[6] Wellcome Sanger Inst, Wellcome Genome Campus, Cambridge CB10 1SA, England
[7] ASTAR, Genome Inst Singapore, Biopolis 138672, Singapore
[8] Univ Cambridge, Dept Biochem, Sanger Bldg, Cambridge CB2 1GA, England
基金
英国惠康基金;
关键词
DNA METHYLATION; IN-VITRO; GENOME-DEFENSE; GENE; PIWI; SPECIFICATION; BIOGENESIS; DYNAMICS; PATHWAY; RECONSTITUTION;
D O I
10.1016/j.devcel.2022.11.004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
PIWI-interacting RNAs (piRNAs) are small RNAs bound by PIWI-clade Argonaute proteins that function to silence transposable elements (TEs). Following mouse primordial germ cell (mPGC) specification around E6.25, fetal piRNAs emerge in male gonocytes from E13.5 onward. The in vitro differentiation of mPGClike cells (mPGCLCs) has raised the possibility of studying the fetal piRNA pathway in greater depth. However, using single-cell RNA-seq and RT-qPCR along mPGCLC differentiation, we find that piRNA pathway factors are not fully expressed in Day 6 mPGCLCs. Moreover, we do not detect piRNAs across a panel of Day 6 mPGCLC lines using small RNA-seq. Our combined efforts highlight that in vitro differentiated Day 6 mPGCLCs do not yet resemble E13.5 or later mouse gonocytes where the piRNA pathway is active. This Matters Arising paper is in response to von Meyenn et al. (2016), published in Developmental Cell. See also the correction by von Meyenn et al. published in this issue.
引用
收藏
页码:2661 / +
页数:13
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