Epididymal acquired sperm microRNAs modify post-fertilization embryonic gene expression

Sperm small RNAs have emerged as important non-genetic contributors to embryogenesis and offspring health. A subset of sperm small RNAs is thought to be acquired during epididymal transit. However, the identity of the specific small RNAs transferred remains unclear. Here, we employ Cre/Lox genetics to generate germline- and epididymal-specific Dgcr8 knockout (KO) mice to investigate the dynamics of sperm microRNAs (miRNAs) and their functions post-fertilization. Testicular sperm from germline Dgcr8 KO mice has reduced levels of 116 miRNAs. Enthrallingly, following epididymal transit, the abundance of 72% of these miRNAs is restored. Conversely, sperm from epididymal Dgcr8 KO mice displayed reduced levels of 27 miRNAs. This loss of epididymal miRNAs in sperm was accompanied by transcriptomic changes in embryos fertilized by this sperm, which was rescued by microinjection of epididymal miRNAs. These findings ultimately demonstrate the acquisition of miRNAs from the soma by sperm during epididymal transit and their subsequent regulation of embryonic gene expression.

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Publication Details

Journal
Cell Reports
Published
2024-09-01
DOI
https://doi.org/10.1016/j.celrep.2024.114698
Citations
27
Primary Topic
MicroRNA in disease regulation
Type
article
Field-Weighted Citation Impact
7.70

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article

Epididymal acquired sperm microRNAs modify post-fertilization embryonic gene expression

Colin C. Conine, Natalie A. Trigg
27 citations
Cell Reports
MicroRNA in disease regulation
7.70
article

Epididymal acquired sperm microRNAs modify post-fertilization embryonic gene expression

Colin C. Conine, Natalie A. Trigg
article en
27 citations

Abstract

Sperm small RNAs have emerged as important non-genetic contributors to embryogenesis and offspring health. A subset of sperm small RNAs is thought to be acquired during epididymal transit. However, the identity of the specific small RNAs transferred remains unclear. Here, we employ Cre/Lox genetics to generate germline- and epididymal-specific Dgcr8 knockout (KO) mice to investigate the dynamics of sperm microRNAs (miRNAs) and their functions post-fertilization. Testicular sperm from germline Dgcr8 KO mice has reduced levels of 116 miRNAs. Enthrallingly, following epididymal transit, the abundance of 72% of these miRNAs is restored. Conversely, sperm from epididymal Dgcr8 KO mice displayed reduced levels of 27 miRNAs. This loss of epididymal miRNAs in sperm was accompanied by transcriptomic changes in embryos fertilized by this sperm, which was rescued by microinjection of epididymal miRNAs. These findings ultimately demonstrate the acquisition of miRNAs from the soma by sperm during epididymal transit and their subsequent regulation of embryonic gene expression.

Cell ReportsVol. 43(9)
Children's Hospital of Philadelphia (US), California Institute for Regenerative Medicine (US), University of Pennsylvania (US)
Pew Charitable Trusts, Children's Hospital of Philadelphia, University of Pennsylvania, National Institutes of Health
Zero hunger
Openalex Percentile: Top 2%
MicroRNA in disease regulation
7.70
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