Transcriptional regulation of the piRNA pathway by Ovo in animal ovarian germ cells

The gene-regulatory mechanisms controlling the expression of the germline PIWI-interacting RNA (piRNA) pathway components within the gonads of metazoan species remain largely unexplored. In contrast to the male germline piRNA pathway, which in mice is known to be activated by the testis-specific transcription factor A-MYB, the nature of the ovary-specific gene-regulatory network driving the female germline piRNA pathway remains a mystery. Here, using <i>Drosophila</i> as a model, we combined multiple genomics approaches to reveal the transcription factor Ovo as regulator of the germline piRNA pathway in ovarian germ cells. Ectopic expression of Ovo in ovarian somatic cells activates germline piRNA pathway components, including the ping-pong factors Aubergine, Argonaute-3, and Vasa, leading to assembly of perinuclear cellular structures resembling nuage bodies of germ cells. We found that in ovarian somatic cells, transcription of <i>ovo</i> is repressed by <i>l(3)mbt</i>, thus preventing expression of germline piRNA pathway genes in the soma. Cross-species ChIP-seq and motif analyses demonstrate that Ovo is binding to genomic CCGTTA motifs within the promoters of germline piRNA pathway genes, suggesting a regulation by Ovo in ovaries analogous to that of A-MYB in testes. Our results also show consistent engagement of the Ovo transcription factor family at ovarian piRNA clusters across metazoan species, reflecting a deep evolutionary conservation of this regulatory paradigm from insects to humans.

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Publication Details

Journal
Genes & Development
Published
2024-12-20
DOI
https://doi.org/10.1101/gad.352120.124
Citations
5
Primary Topic
Chromosomal and Genetic Variations
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article

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article

Transcriptional regulation of the piRNA pathway by Ovo in animal ovarian germ cells

Azad Alizada, Gregory J. Hannon, Benjamin Czech Nicholson
5 citations
Genes & Development
Chromosomal and Genetic Variations
article

Transcriptional regulation of the piRNA pathway by Ovo in animal ovarian germ cells

Azad Alizada, Gregory J. Hannon, Benjamin Czech Nicholson
article en
5 citations

Abstract

The gene-regulatory mechanisms controlling the expression of the germline PIWI-interacting RNA (piRNA) pathway components within the gonads of metazoan species remain largely unexplored. In contrast to the male germline piRNA pathway, which in mice is known to be activated by the testis-specific transcription factor A-MYB, the nature of the ovary-specific gene-regulatory network driving the female germline piRNA pathway remains a mystery. Here, using <i>Drosophila</i> as a model, we combined multiple genomics approaches to reveal the transcription factor Ovo as regulator of the germline piRNA pathway in ovarian germ cells. Ectopic expression of Ovo in ovarian somatic cells activates germline piRNA pathway components, including the ping-pong factors Aubergine, Argonaute-3, and Vasa, leading to assembly of perinuclear cellular structures resembling nuage bodies of germ cells. We found that in ovarian somatic cells, transcription of <i>ovo</i> is repressed by <i>l(3)mbt</i>, thus preventing expression of germline piRNA pathway genes in the soma. Cross-species ChIP-seq and motif analyses demonstrate that Ovo is binding to genomic CCGTTA motifs within the promoters of germline piRNA pathway genes, suggesting a regulation by Ovo in ovaries analogous to that of A-MYB in testes. Our results also show consistent engagement of the Ovo transcription factor family at ovarian piRNA clusters across metazoan species, reflecting a deep evolutionary conservation of this regulatory paradigm from insects to humans.

Genes & DevelopmentVol. 39(3-4)
University of Cambridge (GB), Cancer Research UK (GB)
Wellcome Trust, Cancer Research UK, Cancer Research UK Cambridge Institute, University of Cambridge
Life in Land
Chromosomal and Genetic Variations
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Transcriptional regulation of the piRNA pathway by Ovo in animal ovarian germ cells — Azad Alizada, Gregory J. Hannon, et al. · Genes & Development (2024) | TGRS Research Map | TGRS