Multiple RNA-binding proteins function combinatorially to control the soma-restricted expression pattern of the E3 ligase subunit ZIF-1.
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[1] R. Lin,et al. zif-1 translational repression defines a second, mutually exclusive OMA function in germline transcriptional repression , 2010, Development.
[2] Brian M. Farley,et al. RNA recognition by the embryonic cell fate determinant and germline totipotency factor MEX-3 , 2009, Proceedings of the National Academy of Sciences.
[3] G. Seydoux,et al. Regulation of MBK-2/DYRK by CDK-1 and the Pseudophosphatases EGG-4 and EGG-5 during the Oocyte-to-Embryo Transition , 2009, Cell.
[4] Lesilee S. Rose,et al. An eIF4E-binding protein regulates katanin protein levels in C. elegans embryos , 2009, The Journal of cell biology.
[5] G. Seydoux,et al. Less is more: specification of the germline by transcriptional repression , 2008, Development.
[6] Brian M. Farley,et al. RNA target specificity of the embryonic cell fate determinant POS-1. , 2008, RNA.
[7] G. Seydoux,et al. 3′ UTRs Are the Primary Regulators of Gene Expression in the C. elegans Germline , 2008, Current Biology.
[8] R. Lin,et al. Global Transcriptional Repression in C. elegans Germline Precursors by Regulated Sequestration of TAF-4 , 2008, Cell.
[9] G. Seydoux,et al. Inhibition of Transcription by the Caenorhabditis elegans Germline Protein PIE-1: Genetic Evidence for Distinct Mechanisms Targeting Initiation and Elongation , 2008, Genetics.
[10] R. Lehmann,et al. Germ Versus Soma Decisions: Lessons from Flies and Worms , 2007, Science.
[11] Brian M. Farley,et al. Molecular Basis of RNA Recognition by the Embryonic Polarity Determinant MEX-5* , 2007, Journal of Biological Chemistry.
[12] S. Diede,et al. Reduced Dosage of pos-1 Suppresses Mex Mutants and Reveals Complex Interactions Among CCCH Zinc-Finger Proteins During Caenorhabditis elegans Embryogenesis , 2006, Genetics.
[13] M. Stitzel,et al. The C. elegans DYRK Kinase MBK-2 Marks Oocyte Proteins for Degradation in Response to Meiotic Maturation , 2006, Current Biology.
[14] C. Mello,et al. The Conserved Kinases CDK-1, GSK-3, KIN-19, and MBK-2 Promote OMA-1 Destruction to Regulate the Oocyte-to-Embryo Transition in C. elegans , 2006, Current Biology.
[15] R. Lin,et al. DYRK2 and GSK-3 phosphorylate and promote the timely degradation of OMA-1, a key regulator of the oocyte-to-embryo transition in C. elegans. , 2005, Developmental biology.
[16] S. Strome. Specification of the germ line. , 2005, WormBook : the online review of C. elegans biology.
[17] W. G. Kelly,et al. A conserved chromatin architecture marks and maintains the restricted germ cell lineage in worms and flies. , 2003, Developmental cell.
[18] G. Seydoux,et al. Exclusion of germ plasm proteins from somatic lineages by cullin-dependent degradation , 2003, Nature.
[19] Y. Kohara,et al. Translational control of maternal glp-1 mRNA by POS-1 and its interacting protein SPN-4 in Caenorhabditis elegans , 2003, Development.
[20] R. Lin. A gain-of-function mutation in oma-1, a C. elegans gene required for oocyte maturation, results in delayed degradation of maternal proteins and embryonic lethality. , 2003, Developmental biology.
[21] B. Peterlin,et al. A model of repression: CTD analogs and PIE-1 inhibit transcriptional elongation by P-TEFb. , 2003, Genes & development.
[22] M. Vidal,et al. MEX-3 interacting proteins link cell polarity to asymmetric gene expression in Caenorhabditis elegans. , 2002, Development.
[23] T. Schedl,et al. Identification of in vivo mRNA targets of GLD-1, a maxi-KH motif containing protein required for C. elegans germ cell development. , 2001, Genes & development.
[24] R. Lin,et al. Two zinc finger proteins, OMA-1 and OMA-2, are redundantly required for oocyte maturation in C. elegans. , 2001, Developmental cell.
[25] Elizabeth Casey,et al. Creation of low-copy integrated transgenic lines in Caenorhabditis elegans. , 2001, Genetics.
[26] Morris F. Maduro,et al. Restriction of mesendoderm to a single blastomere by the combined action of SKN-1 and a GSK-3beta homolog is mediated by MED-1 and -2 in C. elegans. , 2001, Molecular cell.
[27] G. Seydoux,et al. Asymmetric segregation of PIE-1 in C. elegans is mediated by two complementary mechanisms that act through separate PIE-1 protein domains. , 2000, Molecular cell.
[28] R. Lin,et al. MEX-5 and MEX-6 function to establish soma/germline asymmetry in early C. elegans embryos. , 2000, Molecular cell.
[29] C. Mello,et al. Transcriptional repression by the Caenorhabditis elegans germ-line protein PIE-1. , 1999, Genes & development.
[30] A. Fire,et al. Specific interference by ingested dsRNA , 1998, Nature.
[31] G. Seydoux,et al. Genetic requirements for PIE-1 localization and inhibition of gene expression in the embryonic germ lineage of Caenorhabditis elegans. , 1998, Developmental biology.
[32] G. Seydoux,et al. Transcriptionally repressed germ cells lack a subpopulation of phosphorylated RNA polymerase II in early embryos of Caenorhabditis elegans and Drosophila melanogaster. , 1997, Development.
[33] W. G. Kelly,et al. Distinct requirements for somatic and germline expression of a generally expressed Caernorhabditis elegans gene. , 1997, Genetics.
[34] J. Priess,et al. The C. elegans MEX-1 protein is present in germline blastomeres and is a P granule component. , 1997, Development.
[35] C. Mello,et al. MEX-3 Is a KH Domain Protein That Regulates Blastomere Identity in Early C. elegans Embryos , 1996, Cell.
[36] C. Mello,et al. The PIE-1 protein and germline specification in C. elegans embryos , 1996, Nature.
[37] A. Fire,et al. Soma-germline asymmetry in the distributions of embryonic RNAs in Caenorhabditis elegans. , 1994, Development.
[38] Harold Weintraub,et al. The pie-1 and mex-1 genes and maternal control of blastomere identity in early C. elegans embryos , 1992, Cell.
[39] Hollis G. Potter,et al. Author Manuscript , 2013 .
[40] C. Mello,et al. pos-1 encodes a cytoplasmic zinc-finger protein essential for germline specification in C. elegans. , 1999, Development.