Deficient spermiogenesis in mice lacking Rlim

The X-linked gene Rlim plays major roles in female mouse development and reproduction, where it is crucial for the maintenance of imprinted X chromosome inactivation in extraembryonic tissues of embryos. However, while females carrying a systemic Rlim knockout (KO) die around implantation, male Rlim...

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Main Authors: Feng Wang, Maria Gracia Gervasi, Ana Bošković, Fengyun Sun, Vera D Rinaldi, Jun Yu, Mary C Wallingford, Darya A Tourzani, Jesse Mager, Lihua Julie Zhu, Oliver J Rando, Pablo E Visconti, Lara Strittmatter, Ingolf Bach
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2021-02-01
Series:eLife
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Online Access:https://elifesciences.org/articles/63556
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author Feng Wang
Maria Gracia Gervasi
Ana Bošković
Fengyun Sun
Vera D Rinaldi
Jun Yu
Mary C Wallingford
Darya A Tourzani
Jesse Mager
Lihua Julie Zhu
Oliver J Rando
Pablo E Visconti
Lara Strittmatter
Ingolf Bach
author_facet Feng Wang
Maria Gracia Gervasi
Ana Bošković
Fengyun Sun
Vera D Rinaldi
Jun Yu
Mary C Wallingford
Darya A Tourzani
Jesse Mager
Lihua Julie Zhu
Oliver J Rando
Pablo E Visconti
Lara Strittmatter
Ingolf Bach
author_sort Feng Wang
collection DOAJ
description The X-linked gene Rlim plays major roles in female mouse development and reproduction, where it is crucial for the maintenance of imprinted X chromosome inactivation in extraembryonic tissues of embryos. However, while females carrying a systemic Rlim knockout (KO) die around implantation, male Rlim KO mice appear healthy and are fertile. Here, we report an important role for Rlim in testis where it is highly expressed in post-meiotic round spermatids as well as in Sertoli cells. Systemic deletion of the Rlim gene results in lower numbers of mature sperm that contains excess cytoplasm, leading to decreased sperm motility and in vitro fertilization rates. Targeting the conditional Rlim cKO specifically to the spermatogenic cell lineage largely recapitulates this phenotype. These results reveal functions of Rlim in male reproduction specifically in round spermatids during spermiogenesis.
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spelling doaj.art-85c0317343a64841b13715f36fcb38902022-12-22T03:51:17ZengeLife Sciences Publications LtdeLife2050-084X2021-02-011010.7554/eLife.63556Deficient spermiogenesis in mice lacking RlimFeng Wang0Maria Gracia Gervasi1https://orcid.org/0000-0002-5468-2700Ana Bošković2Fengyun Sun3Vera D Rinaldi4https://orcid.org/0000-0002-0051-1754Jun Yu5Mary C Wallingford6Darya A Tourzani7Jesse Mager8Lihua Julie Zhu9Oliver J Rando10https://orcid.org/0000-0003-1516-9397Pablo E Visconti11Lara Strittmatter12Ingolf Bach13https://orcid.org/0000-0003-4505-8946Department of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, United StatesDepartment of Veterinary & Animal Sciences, University of Massachusetts Amherst, Amherst, United StatesDepartment of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, United StatesDepartment of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, United StatesDepartment of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, United StatesDepartment of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, United StatesDepartment of Veterinary & Animal Sciences, University of Massachusetts Amherst, Amherst, United StatesDepartment of Veterinary & Animal Sciences, University of Massachusetts Amherst, Amherst, United StatesDepartment of Veterinary & Animal Sciences, University of Massachusetts Amherst, Amherst, United StatesDepartment of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, United States; Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, United States; Program in Bioinformatics and Integrative Biology, University of Massachusetts Medical School, Worcester, United StatesDepartment of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, United StatesDepartment of Veterinary & Animal Sciences, University of Massachusetts Amherst, Amherst, United StatesElectron Microscopy Core, University of Massachusetts Medical School, Worcester, United StatesDepartment of Molecular, Cell and Cancer Biology, University of Massachusetts Medical School, Worcester, United States; Program in Molecular Medicine, University of Massachusetts Medical School, Worcester, United StatesThe X-linked gene Rlim plays major roles in female mouse development and reproduction, where it is crucial for the maintenance of imprinted X chromosome inactivation in extraembryonic tissues of embryos. However, while females carrying a systemic Rlim knockout (KO) die around implantation, male Rlim KO mice appear healthy and are fertile. Here, we report an important role for Rlim in testis where it is highly expressed in post-meiotic round spermatids as well as in Sertoli cells. Systemic deletion of the Rlim gene results in lower numbers of mature sperm that contains excess cytoplasm, leading to decreased sperm motility and in vitro fertilization rates. Targeting the conditional Rlim cKO specifically to the spermatogenic cell lineage largely recapitulates this phenotype. These results reveal functions of Rlim in male reproduction specifically in round spermatids during spermiogenesis.https://elifesciences.org/articles/63556Rlimspermiogenesiscytoplasmic reductionmouse genetics
spellingShingle Feng Wang
Maria Gracia Gervasi
Ana Bošković
Fengyun Sun
Vera D Rinaldi
Jun Yu
Mary C Wallingford
Darya A Tourzani
Jesse Mager
Lihua Julie Zhu
Oliver J Rando
Pablo E Visconti
Lara Strittmatter
Ingolf Bach
Deficient spermiogenesis in mice lacking Rlim
eLife
Rlim
spermiogenesis
cytoplasmic reduction
mouse genetics
title Deficient spermiogenesis in mice lacking Rlim
title_full Deficient spermiogenesis in mice lacking Rlim
title_fullStr Deficient spermiogenesis in mice lacking Rlim
title_full_unstemmed Deficient spermiogenesis in mice lacking Rlim
title_short Deficient spermiogenesis in mice lacking Rlim
title_sort deficient spermiogenesis in mice lacking rlim
topic Rlim
spermiogenesis
cytoplasmic reduction
mouse genetics
url https://elifesciences.org/articles/63556
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