Evidence that mouse Bmp8a (Op2) and Bmp8b are duplicated genes that play a role in spermatogenesis and placental development
- PMID: 8843393
- DOI: 10.1016/0925-4773(96)00543-6
Evidence that mouse Bmp8a (Op2) and Bmp8b are duplicated genes that play a role in spermatogenesis and placental development
Abstract
We have identified two highly conserved mouse genes encoding bone morphogenetic protein 8A (BMP8A/OP2) and 8B (BMP8B). The two loci are tightly linked on chromosome 4, suggesting that they arose through a recent gene duplication. Contrary to previous reports, neither gene is expressed in the early postimplantation mouse embryo (7.5-10.5 days post coitum) as judged by a variety of sensitive techniques. By contrast, high levels of Bmp8b RNA are found in the decidual cells of the uterus, and both genes are expressed in the trophoblast cells of the labyrinthine region of the placenta and in the inner root sheath of hair follicles of early postnatal skin. In addition, both Bmp8a and Bmp8b are expressed in the testis during specific stages of spermatogenesis, with the highest levels of RNA in stage 6-8 round spermatids after 3 weeks of age. Bmp8a and 8b are, therefore, the first members of the transforming growth factor beta (TGF beta)-related gene family to be found expressed in the germ cells of the testis, rather than in the somatic Sertoli cells. These results suggest that Bmp8a and 8b are not required for development of the embryo proper but regulate aspects of cell proliferation, survival and/or differentiation during spermatogenesis and placentation.
Similar articles
-
Bone morphogenetic protein 8A plays a role in the maintenance of spermatogenesis and the integrity of the epididymis.Development. 1998 Mar;125(6):1103-12. doi: 10.1242/dev.125.6.1103. Development. 1998. PMID: 9463357
-
The gene encoding bone morphogenetic protein 8B is required for the initiation and maintenance of spermatogenesis in the mouse.Genes Dev. 1996 Jul 1;10(13):1657-69. doi: 10.1101/gad.10.13.1657. Genes Dev. 1996. PMID: 8682296
-
BMP8A sustains spermatogenesis by activating both SMAD1/5/8 and SMAD2/3 in spermatogonia.Sci Signal. 2017 May 2;10(477):eaal1910. doi: 10.1126/scisignal.aal1910. Sci Signal. 2017. PMID: 28465413
-
Bone morphogenetic proteins.Growth Factors. 2004 Dec;22(4):233-41. doi: 10.1080/08977190412331279890. Growth Factors. 2004. PMID: 15621726 Review.
-
Drivers of germ cell maturation.Ann N Y Acad Sci. 2005 Dec;1061:173-82. doi: 10.1196/annals.1336.018. Ann N Y Acad Sci. 2005. PMID: 16467266 Review.
Cited by
-
Defining BMP functions in the hair follicle by conditional ablation of BMP receptor IA.J Cell Biol. 2003 Nov 10;163(3):609-23. doi: 10.1083/jcb.200309042. J Cell Biol. 2003. PMID: 14610062 Free PMC article.
-
Identifying concerted evolution and gene conversion in mammalian gene pairs lasting over 100 million years.BMC Evol Biol. 2009 Jul 7;9:156. doi: 10.1186/1471-2148-9-156. BMC Evol Biol. 2009. PMID: 19583854 Free PMC article.
-
Genetic interplays between Msx2 and Foxn1 are required for Notch1 expression and hair shaft differentiation.Dev Biol. 2009 Feb 15;326(2):420-30. doi: 10.1016/j.ydbio.2008.11.021. Epub 2008 Dec 7. Dev Biol. 2009. PMID: 19103190 Free PMC article.
-
Smad1 and 5 but not Smad8 establish stem cell quiescence which is critical to transform the premature hair follicle during morphogenesis toward the postnatal state.Stem Cells. 2014 Feb;32(2):534-47. doi: 10.1002/stem.1548. Stem Cells. 2014. PMID: 24023003 Free PMC article.
-
Induction of primordial germ cells from murine epiblasts by synergistic action of BMP4 and BMP8B signaling pathways.Proc Natl Acad Sci U S A. 2001 Jul 3;98(14):7858-62. doi: 10.1073/pnas.151242798. Epub 2001 Jun 26. Proc Natl Acad Sci U S A. 2001. PMID: 11427739 Free PMC article.
Publication types
MeSH terms
Substances
Associated data
- Actions
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Molecular Biology Databases
