4.7 Article

Sdmg1 is a conserved transmembrane protein associated with germ cell sex determination and germline-soma interactions in mice

Journal

DEVELOPMENT
Volume 135, Issue 8, Pages 1415-1425

Publisher

COMPANY OF BIOLOGISTS LTD
DOI: 10.1242/dev.019497

Keywords

mouse; primordial germ cells; sertoli cell; membrane trafficking; sdmg1 (Tmem184a)

Funding

  1. Medical Research Council [G120/952, MC_U127580973] Funding Source: researchfish
  2. MRC [MC_U127580973, G120/952] Funding Source: UKRI
  3. Medical Research Council [G120/952, U.1275.01.008(80973), MC_U127580973, MC_PC_U127580973] Funding Source: Medline
  4. Wellcome Trust Funding Source: Medline

Ask authors/readers for more resources

In mammals, the supporting cell lineage in an embryonic gonad communicates the sex-determining decision to various sexually dimorphic cell types in the developing embryo, including the germ cells. However, the molecular nature of the sex-determining signals that pass from the supporting cells to the germ cells is not well understood. We have identified a conserved transmembrane protein, Sdmg1, owing to its male-specific expression in mouse embryonic gonads. Sdmg1 is expressed in the Sertoli cells of embryonic testes from 12.5 dpc, and in granulosa cells of growing follicles in adult ovaries. In Sertoli cells, Sdmg1 is localised to endosomes, and knock-down of Sdmg1 in Sertoli cell lines causes mis-localisation of the secretory SNARE Stx2 and defects in membrane trafficking. Upregulation of Sdmg1 appears to be part of a larger programme of changes to membrane trafficking pathways in embryonic Sertoli cells, and perturbing secretion in male embryonic gonads in organ culture causes male-to-female germ cell sex reversal. These data suggest that changes that occur in the cell biology of embryonic Sertoli cells may facilitate the communication of male sex-determining decisions to the germ cells during embryonic development.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available