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Xcat2 RNA is a translationally sequestered germ plasm component in Xenopus
Journal article   Open access   Peer reviewed

Xcat2 RNA is a translationally sequestered germ plasm component in Xenopus

H MacArthur, M Bubunenko, D W Houston and M L King
Mechanisms of development, Vol.84(1-2), pp.75-88
06/1999
DOI: 10.1016/S0925-4773(99)00075-1
PMID: 10473122
url
https://doi.org/10.1016/S0925-4773(99)00075-1View
Published (Version of record) Open Access

Abstract

In Xenopus, the inheritance of germ plasm by a small subset of blastomeres during early development is thought to direct these cells into the germ cell lineage. We show that Xcat2 RNA, related to Drosophila nanos, is a germ plasm component that is translationally repressed during oogenesis. Xcat2 protein was not detected in oocytes at times prior to, or after its RNA was localized in germ plasm, suggesting Xcat2 RNA is functionally sequestered soon after transcription. Indeed, Xcat2 RNA is found in a dense non-polysomal compartment in oocytes. Repression of translation was not relieved by substituting the Xcat2 3'UTR with that of beta-globin. Immunodetection of Xcat2 protein during blastula and gastrula stages coincides with the time of symmetric segregation of the germ plasm and a net increase in the number of primordial germ cells. Xcat2 is capable of binding RNA in vitro and we propose that it may function to translationally regulate other RNAs specific to primordial germ cells.
Drosophila Proteins Protein Biosynthesis Zinc Fingers Immune Sera Xenopus - genetics RNA, Messenger - genetics Cell Cycle Proteins - metabolism Insect Proteins - genetics RNA-Binding Proteins Oogenesis - genetics RNA, Messenger - metabolism Xenopus - embryology Cell Compartmentation Oocytes - cytology Injections Animals Oocytes - physiology Gene Expression Regulation, Developmental Embryo, Nonmammalian Cell Cycle Proteins - genetics Female Germ Cells - metabolism 3' Untranslated Regions

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