Literature DB >> 25310986

The SET-2/SET1 histone H3K4 methyltransferase maintains pluripotency in the Caenorhabditis elegans germline.

Valérie J Robert1, Marine G Mercier1, Cécile Bedet1, Stéphane Janczarski1, Jorge Merlet2, Steve Garvis1, Rafal Ciosk2, Francesca Palladino3.   

Abstract

Histone H3 Lys 4 methylation (H3K4me) is deposited by the conserved SET1/MLL methyltransferases acting in multiprotein complexes, including Ash2 and Wdr5. Although individual subunits contribute to complex activity, how they influence gene expression in specific tissues remains largely unknown. In Caenorhabditis elegans, SET-2/SET1, WDR-5.1, and ASH-2 are differentially required for germline H3K4 methylation. Using expression profiling on germlines from animals lacking set-2, ash-2, or wdr-5.1, we show that these subunits play unique as well as redundant functions in order to promote expression of germline genes and repress somatic genes. Furthermore, we show that in set-2- and wdr-5.1-deficient germlines, somatic gene misexpression is associated with conversion of germ cells into somatic cells and that nuclear RNAi acts in parallel with SET-2 and WDR-5.1 to maintain germline identity. These findings uncover a unique role for SET-2 and WDR-5.1 in preserving germline pluripotency and underline the complexity of the cellular network regulating this process.

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Year:  2014        PMID: 25310986     DOI: 10.1016/j.celrep.2014.09.018

Source DB:  PubMed          Journal:  Cell Rep            Impact factor:   9.423


  22 in total

Review 1.  Epigenetic regulation of ageing: linking environmental inputs to genomic stability.

Authors:  Bérénice A Benayoun; Elizabeth A Pollina; Anne Brunet
Journal:  Nat Rev Mol Cell Biol       Date:  2015-09-16       Impact factor: 94.444

Review 2.  Repression of somatic cell fate in the germline.

Authors:  Valérie J Robert; Steve Garvis; Francesca Palladino
Journal:  Cell Mol Life Sci       Date:  2015-06-05       Impact factor: 9.261

3.  Natural Genetic Variation in a Multigenerational Phenotype in C. elegans.

Authors:  Lise Frézal; Emilie Demoinet; Christian Braendle; Eric Miska; Marie-Anne Félix
Journal:  Curr Biol       Date:  2018-08-02       Impact factor: 10.834

4.  PLP-1 is essential for germ cell development and germline gene silencing in Caenorhabditis elegans.

Authors:  Rajaram Vishnupriya; Linitha Thomas; Lamia Wahba; Andrew Fire; Kuppuswamy Subramaniam
Journal:  Development       Date:  2020-11-27       Impact factor: 6.868

5.  SET-9 and SET-26 are H3K4me3 readers and play critical roles in germline development and longevity.

Authors:  Wenke Wang; Amaresh Chaturbedi; Minghui Wang; Serim An; Satheeja Santhi Velayudhan; Siu Sylvia Lee
Journal:  Elife       Date:  2018-05-01       Impact factor: 8.140

Review 6.  Developmental Plasticity and Cellular Reprogramming in Caenorhabditis elegans.

Authors:  Joel Rothman; Sophie Jarriault
Journal:  Genetics       Date:  2019-11       Impact factor: 4.562

Review 7.  Specifying and protecting germ cell fate.

Authors:  Susan Strome; Dustin Updike
Journal:  Nat Rev Mol Cell Biol       Date:  2015-07       Impact factor: 94.444

8.  Germ Granules Prevent Accumulation of Somatic Transcripts in the Adult Caenorhabditis elegans Germline.

Authors:  Andrew Kekūpa'a Knutson; Thea Egelhofer; Andreas Rechtsteiner; Susan Strome
Journal:  Genetics       Date:  2017-03-03       Impact factor: 4.562

9.  Multiple Histone Methyl-Lysine Readers Ensure Robust Development and Germline Immortality in Caenorhabditis elegans.

Authors:  Arneet L Saltzman; Mark W Soo; Reta Aram; Jeannie T Lee
Journal:  Genetics       Date:  2018-09-05       Impact factor: 4.562

10.  The balance of poly(U) polymerase activity ensures germline identity, survival and development in Caenorhabditis elegans.

Authors:  Yini Li; Eleanor M Maine
Journal:  Development       Date:  2018-10-10       Impact factor: 6.868

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