A conserved node in the regulation of Vasa between an induced and an inherited program of primordial germ cell specification.
A conserved node in the regulation of Vasa between an induced and an inherited program of primordial germ cell specification.
复制标题
在诱导的原始生殖细胞规范和遗传程序之间对VASA调节中的保守节点。
DOI:
10.1016/j.ydbio.2021.11.007
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发表时间:
2022-03
影响因子:
2.7
通讯作者:
Wessel GM
中科院分区:
文献类型:
--
作者:
Perillo M;Swartz SZ;Wessel GM
Primordial germ cells (PGCs) are specified by diverse mechanisms in early development. In some animals, PGCs are specified via inheritance of maternal determinants, while in others, in a process thought to represent the ancestral mode, PGC fate is induced by cell interactions. Although the terminal factors expressed in specified germ cells are widely conserved, the mechanisms by which these factors are regulated can be widely diverse. Here we show that a post-translational mechanism of germ cell specification is conserved between two echinoderm species thought to employ divergent germ line segregation strategies. Sea urchins segregate their germ line early by an inherited mechanism. The DEAD-box RNA - helicase Vasa, a conserved germline factor, becomes enriched in the PGCs by degradation in future somatic cells by the E3-ubiquitin-ligase Gustavus. This post-translational activity occurs early in development, substantially prior to gastrulation. Here we test this process in germ cell specification of sea star embryos, which tive signaling mechanisms after gastrulation for PGC fate determination. We find that Vasa-GFP protein becomes restricted to the PGCs in the sea star even though the injected mRNA is present throughout the embryo. Gustavus depletion, however, results in uniform accumulation of the protein. These data demonstrate that Gustavus-mediated Vasa turnover in somatic cells is conserved between species with otherwise divergent PGC specification mechanisms. Since Gustavus was originally identified in Drosophila melanogaster to have similar functions in Vasa regulation, we conclude that this node of Vasa regulation in PGC formation is ancestral and evolutionarily transposable from the ancestral, induced PGC specification program to an inherited PGC specification mechanism.
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影响因子:
14.9
作者:
Cameron RA;Samanta M;Yuan A;He D;Davidson E
通讯作者:
Davidson E
DOI:
10.1007/978-1-0716-0974-3_12
发表时间:
2021
期刊:
Methods in molecular biology (Clifton, N.J.)
影响因子:
--
作者:
Perillo M;Paganos P;Spurrell M;Arnone MI;Wessel GM
通讯作者:
Wessel GM
DOI:
10.1093/database/bax074
发表时间:
2017-01-01
期刊:
Database : the journal of biological databases and curation
影响因子:
--
作者:
Kudtarkar P;Cameron RA
通讯作者:
Cameron RA
影响因子:
2.7
作者:
Gustafson EA;Yajima M;Juliano CE;Wessel GM
通讯作者:
Wessel GM
影响因子:
4.6
作者:
Fresques, Tara M.;Wessel, Gary M.
通讯作者:
Wessel, Gary M.