scholarly journals The C. elegans CSR-1 Argonaute Pathway Counteracts Epigenetic Silencing to Promote Germline Gene Expression

2013 ◽  
Vol 27 (6) ◽  
pp. 656-663 ◽  
Author(s):  
Meetu Seth ◽  
Masaki Shirayama ◽  
Weifeng Gu ◽  
Takao Ishidate ◽  
Darryl Conte ◽  
...  
Keyword(s):  
Gene Expression ◽  
Epigenetic Silencing ◽  
Germline Gene ◽  
C Elegans

scholarly journals C. elegans synMuv B proteins regulate spatial and temporal chromatin compaction during development

2019 ◽  
Author(s):  
Meghan E. Costello ◽  
Lisa N. Petrella
Keyword(s):  
Gene Expression ◽  
Cell Fate ◽  
Developmental Time ◽  
Somatic Tissue ◽  
Temperature Sensitive ◽  
Germline Gene ◽  
Tissue Specific ◽  
Chromatin Compaction ◽  
C Elegans ◽  
Repressive Chromatin

AbstractTissue-specific establishment of repressive chromatin through creation of compact chromatin domains during development is necessary to ensure proper gene expression and cell fate. C. elegans synMuv B proteins are important for the soma/germline fate decision and mutants demonstrate ectopic germline gene expression in somatic tissue, especially at high temperature. We show that C. elegans synMuv B proteins regulate developmental chromatin compaction and that timing of chromatin compaction is temperature sensitive in both wild-type and synMuv B mutants. Chromatin compaction in mutants is delayed into developmental time-periods when zygotic gene expression is upregulated and demonstrates an anterior-to-posterior pattern. Loss of this patterned compaction coincides with the developmental time-period of ectopic germline gene expression that leads to a developmental arrest in synMuv B mutants. Thus, chromatin organization throughout development is regulated both spatially and temporally by synMuv B proteins to establish repressive chromatin in a tissue-specific manner to ensure proper gene expression.

scholarly journals Argonautes Promote Male Fertility and Provide a Paternal Memory of Germline Gene Expression in C. elegans

Cell ◽  
2013 ◽  
Vol 155 (7) ◽  
pp. 1532-1544 ◽  
Author(s):  
Colin C. Conine ◽  
James J. Moresco ◽  
Weifeng Gu ◽  
Masaki Shirayama ◽  
Darryl Conte ◽  
...  
Keyword(s):  
Gene Expression ◽  
Male Fertility ◽  
Germline Gene ◽  
C Elegans

scholarly journals A Global Profile of Germline Gene Expression in C. elegans

2000 ◽  
Vol 6 (3) ◽  
pp. 605-616 ◽  
Author(s):  
Valerie Reinke ◽  
Harold E. Smith ◽  
Jeremy Nance ◽  
John Wang ◽  
Carrie Van Doren ◽  
...  
Keyword(s):  
Gene Expression ◽  
Germline Gene ◽  
C Elegans ◽  
Global Profile

scholarly journals Protection of Germline Gene Expression by the C. elegans Argonaute CSR-1

2013 ◽  
Vol 27 (6) ◽  
pp. 664-671 ◽  
Author(s):  
Christopher J. Wedeles ◽  
Monica Z. Wu ◽  
Julie M. Claycomb
Keyword(s):  
Gene Expression ◽  
Germline Gene ◽  
C Elegans

scholarly journals A global chromatin compaction pathway that represses germline gene expression during starvation

2021 ◽  
Vol 220 (9) ◽  
Author(s):  
Mezmur D. Belew ◽  
Emilie Chien ◽  
Matthew Wong ◽  
W. Matthew Michael
Keyword(s):  
Gene Expression ◽  
Topoisomerase Ii ◽  
Germline Gene ◽  
Regulate Gene Expression ◽  
Chromatin Compaction ◽  
C Elegans ◽  
Genome Wide ◽  
A Genome ◽  
Energy Sensing ◽  
Heterochromatin Assembly

While much is known about how transcription is controlled at individual genes, comparatively little is known about how cells regulate gene expression on a genome-wide level. Here, we identify a molecular pathway in the C. elegans germline that controls transcription globally in response to nutritional stress. We report that when embryos hatch into L1 larvae, they sense the nutritional status of their environment, and if food is unavailable, they repress gene expression via a global chromatin compaction (GCC) pathway. GCC is triggered by the energy-sensing kinase AMPK and is mediated by a novel mechanism that involves the topoisomerase II/condensin II axis acting upstream of heterochromatin assembly. When the GCC pathway is inactivated, then transcription persists during starvation. These results define a new mode of whole-genome control of transcription.

scholarly journals Intercellular transport of RNA can limit heritable epigenetic changes

2021 ◽  
Author(s):  
Nathan Shugarts ◽  
Andrew L. Yi ◽  
Winnie M. Chan ◽  
Julia A. Marré ◽  
Aishwarya Sathya ◽  
...  
Keyword(s):  
Gene Expression ◽  
Substrate Specificity ◽  
Extracellular Space ◽  
Epigenetic Changes ◽  
Germline Gene ◽  
Intercellular Transport ◽  
Rna Regulation ◽  
Double Stranded Rna ◽  
C Elegans ◽  
Regulatory Information

AbstractRNAs in circulation carry sequence-specific regulatory information between cells in animal, plant, and host-pathogen systems. Double-stranded RNA (dsRNA) delivered into the extracellular space of the nematode C. elegans accumulates within the germline and reaches progeny. Here we provide evidence for spatial, temporal, and substrate specificity in the transport of dsRNA from parental circulation to progeny. Temporary loss of dsRNA transport resulted in the persistent accumulation of mRNA from a germline gene. The expression of this gene varied among siblings and even between gonad arms within one animal. Perturbing RNA regulation of the gene created new epigenetic states that lasted for many generations. Thus, one role for the transport of dsRNA into the germline in every generation is to limit heritable changes in gene expression.One Sentence SummaryRNA from parental circulation reduces heritable changes in gene expression.

scholarly journals Identification of piRNA binding sites reveals the Argonaute regulatory landscape of the C. elegans germline

2018 ◽  
Author(s):  
En-Zhi Shen ◽  
Hao Chen ◽  
Ahmet R. Ozturk ◽  
Shikui Tu ◽  
Masaki Shirayama ◽  
...  
Keyword(s):  
Gene Expression ◽  
Binding Sites ◽  
Small Rnas ◽  
Cross Linking ◽  
Computational Studies ◽  
Germline Gene ◽  
C Elegans ◽  
Transcriptional Regulatory ◽  
Regulatory Landscape

SUMMARYpiRNAs (Piwi-interacting small RNAs) engage Piwi Argonautes to silence transposons and promote fertility in animal germlines. Genetic and computational studies have suggested that C. elegans piRNAs tolerate mismatched pairing and in principle could target every transcript. Here we employ in vivo cross-linking to identify transcriptome-wide interactions between piRNAs and target RNAs. We show that piRNAs engage all germline mRNAs and that piRNA binding follows microRNA-like pairing rules. Targeting correlates better with binding energy than with piRNA abundance, suggesting that piRNA concentration does not limit targeting. In mRNAs silenced by piRNAs, secondary small RNAs accumulate at the center and ends of piRNA binding sites. In germline-expressed mRNAs, however, targeting by the CSR-1 Argonaute correlates with reduced piRNA binding density and suppression of piRNA-associated secondary small RNAs. Our findings reveal physiologically important and nuanced regulation of individual piRNA targets and provide evidence for a comprehensive post transcriptional regulatory step in germline gene expression.

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