Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Echinobase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Echinobase
ECB-ART-41375
Dev Biol 2010 Jan 15;3372:220-32. doi: 10.1016/j.ydbio.2009.10.030.
Show Gene links Show Anatomy links

Nanos functions to maintain the fate of the small micromere lineage in the sea urchin embryo.



Abstract
The translational regulator nanos is required for the survival and maintenance of primordial germ cells during embryogenesis. Three nanos homologs are present in the genome of the sea urchin Strongylocentrotus purpuratus, all of which are expressed with different timing in the small micromere lineage. This lineage is set-aside during embryogenesis and contributes to constructing the adult rudiment. Small micromeres lacking Sp-nanos1 and Sp-nanos2 undergo an extra division and are not incorporated into the coelomic pouches. Further, these cells do not accumulate Vasa protein even though they retain vasa mRNA. Larvae that develop from Sp-nanos1 and 2 knockdown embryos initially appear normal, but do not develop adult rudiments; although they are capable of eating, over time they fail to grow and eventually die. We conclude that the acquisition and maintenance of multipotency in the small micromere lineage requires nanos, which may function in part by repressing the cell cycle and regulating other multipotency factors such as vasa. This work, in combination with other recent results in Ilyanassa and Platynereis dumerilii, suggests the presence of a conserved molecular program underlying both primordial germ cell and multipotent cell specification and maintenance.

PubMed ID: 19878662
PMC ID: PMC2812692
Article link: Dev Biol
Grant support: [+]

Genes referenced: ddx4 LOC100887844 LOC115919123 LOC115919910 LOC583082 nanos2l
Antibodies: ddx4 Ab1 ddx4 Ab2 nanos2l Ab1

References [+] :
Altschul, Basic local alignment search tool. 1990, Pubmed