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1.
Development ; 144(2): 292-304, 2017 01 15.
Article in English | MEDLINE | ID: mdl-28096217

ABSTRACT

During oogenesis, hundreds of maternal RNAs are selectively localized to the animal or vegetal pole, including determinants of somatic and germline fates. Although microarray analysis has identified localized determinants, it is not comprehensive and is limited to known transcripts. Here, we utilized high-throughput RNA-sequencing analysis to comprehensively interrogate animal and vegetal pole RNAs in the fully grown Xenopus laevis oocyte. We identified 411 (198 annotated) and 27 (15 annotated) enriched mRNAs at the vegetal and animal pole, respectively. Ninety were novel mRNAs over 4-fold enriched at the vegetal pole and six were over 10-fold enriched at the animal pole. Unlike mRNAs, microRNAs were not asymmetrically distributed. Whole-mount in situ hybridization confirmed that all 17 selected mRNAs were localized. Biological function and network analysis of vegetally enriched transcripts identified protein-modifying enzymes, receptors, ligands, RNA-binding proteins, transcription factors and co-factors with five defining hubs linking 47 genes in a network. Initial functional studies of maternal vegetally localized mRNAs show that sox7 plays a novel and important role in primordial germ cell (PGC) development and that ephrinB1 (efnb1) is required for proper PGC migration. We propose potential pathways operating at the vegetal pole that highlight where future investigations might be most fruitful.


Subject(s)
Cell Movement/genetics , Embryonic Germ Cells/physiology , Germ Cells/metabolism , RNA, Messenger, Stored/genetics , RNA/metabolism , Xenopus laevis , Animals , Animals, Genetically Modified , Embryonic Germ Cells/metabolism , Female , High-Throughput Nucleotide Sequencing , Oocytes/metabolism , Oogenesis/genetics , RNA/analysis , RNA/genetics , RNA, Messenger, Stored/metabolism , Xenopus laevis/embryology , Xenopus laevis/genetics
2.
Methods Mol Biol ; 1463: 115-124, 2017.
Article in English | MEDLINE | ID: mdl-27734352

ABSTRACT

Primordial germ cells (PGCs) are the precursors to the gametes and have the unique ability to retain full developmental potential. However, the mechanism(s) and gene-network(s) necessary for their proper specification and development are poorly understood. This is due, in part, to the challenges that must be overcome in order to identify and isolate PGCs during critical stages of development. Two distinct mechanisms have been characterized to specify the germ cell lineage in vertebrates: induction and inheritance. Regardless of mechanism, there are common developmental features shared among all vertebrates in forming the germ cell lineage. Xenopus offers several advantages for understanding the molecular mechanisms necessary to establish the germ line. Here, we provide detailed methods for isolating live PGCs at different time points: 1) just after they have segregated from the endodermal lineage, and 2) while they are migrating towards the presumptive gonad. Isolation of PGCs at these critical developmental stages will allow for the investigation of the mechanism(s) and gene-network(s) necessary for their proper specification and development.


Subject(s)
Cell Separation/methods , Germ Cells/cytology , Xenopus laevis/embryology , Animals , Cell Differentiation , Cell Lineage , Cell Movement , Endoderm/cytology , Gene Expression Regulation, Developmental , Germ Cells/growth & development , Stem Cells/cytology
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