IGSF11 is required for pericentric heterochromatin dissociation during meiotic diplotene

PLoS Genet. 2021 Sep 7;17(9):e1009778. doi: 10.1371/journal.pgen.1009778. eCollection 2021 Sep.

Abstract

Meiosis initiation and progression are regulated by both germ cells and gonadal somatic cells. However, little is known about what genes or proteins connecting somatic and germ cells are required for this regulation. Our results show that deficiency for adhesion molecule IGSF11, which is expressed in both Sertoli cells and germ cells, leads to male infertility in mice. Combining a new meiotic fluorescent reporter system with testicular cell transplantation, we demonstrated that IGSF11 is required in both somatic cells and spermatogenic cells for primary spermatocyte development. In the absence of IGSF11, spermatocytes proceed through pachytene, but the pericentric heterochromatin of nonhomologous chromosomes remains inappropriately clustered from late pachytene onward, resulting in undissolved interchromosomal interactions. Hi-C analysis reveals elevated levels of interchromosomal interactions occurring mostly at the chromosome ends. Collectively, our data elucidates that IGSF11 in somatic cells and germ cells is required for pericentric heterochromatin dissociation during diplotene in mouse primary spermatocytes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Adhesion Molecules / genetics
  • Cell Adhesion Molecules / physiology*
  • Chromosomes
  • Female
  • Genes, Reporter
  • Heterochromatin / metabolism*
  • Humans
  • Immunoglobulins / genetics
  • Immunoglobulins / physiology*
  • Male
  • Meiotic Prophase I*
  • Mice
  • Sertoli Cells / metabolism
  • Spermatocytes / metabolism

Substances

  • Cell Adhesion Molecules
  • Heterochromatin
  • IGSF11 protein, human
  • Immunoglobulins

Grants and funding

This work was supported by the Ministry of Science and Technology of China (2018YFA0107703) to K.K.; National Natural Science Foundation of China (Grant number: 82071597) to K.K. Research in K.K. lab is partly supported by Tsinghua-Peking Center for Life Sciences. The funders played no role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript.