The Expression of a Mitochondria-Localized Glutamic Acid-Rich Protein (MGARP/OSAP) Is Under the Regulation of the HPG Axis. Zhou M et al. The hypothalamic-pituitary-gonadal (HPG) axis exerts a profound effect on animal development, reproduction, and response to stress, and new insights into its complicated functional activities are continuously being made. In the present study, by using immunohistochemical studies and different mouse models (ovariectomy and ob/ob mice), we systemically analyzed the expression of a novel mitochondria-localized glutamic acid-rich protein (MGARP)/ovary-specific acid protein and demonstrated that MGARP is under the regulation of the HPG axis. MGARP is highly enriched in steroidogenic tissues and the visual system. Interestingly, its expression increases as mice develop. Early in development, MGARP is mainly detected in the retina and adrenal gland. At this early developmental stage, its expression is not detectable in the gonads, but its expression in the gonads dramatically increases during the first 2-4 wk after birth. Importantly, MGARP levels correlate with estrogen levels in the ovaries during the estrous cycle, and estrogen regulates the expression of MGARP in a tissue-specific manner and through a feedback regulatory mechanism. Functional inhibition of GnRH with an antagonist strongly reduces MGARP levels, and knockout of leptin (ob/ob) significantly reduces the MGARP expression in follicular granular cells. We proposed a model that elucidates the role MGARP plays in the HPG axis. Within the HPG axis loop, MGARP participates in hormone biosynthesis while being under the regulation of the hormones derived from the HPG axis.
Ovarian localization
Comment
Cloning, Sequence, and Association Analysis of Porcine OSAP Gene. Lei Y et al. Ovary-specific acidic protein (OSAP) is an important reproduction-related gene. In this study, we cloned the full-length cDNA sequence of porcine OSAP gene through the rapid amplification of cDNA ends method. The porcine OSAP gene encodes a protein of 238 amino acids which shares high homology with the OSAP of five species: rhesus monkey (72%), human (70%), cattle (68%), horse (68%), and dog (61%). This gene is structured in four exons and three introns as revealed by computer-assisted analysis. PCR-RFLP was established to detect the GU373669:c.854A>T substitution of porcine OSAP gene mRNA and association of this mutation with litter size traits was assessed in Large White (n?=?100) and Landrace (n?=?100) pig populations. Results demonstrated that this polymorphic locus was significantly associated with the litter size of all parities in Large White sows and Landrace sows (P?0.05). Therefore, OSAP gene could be a useful candidate gene in selection for increasing litter size in pigs. These data serve as a foundation for further insight into this novel porcine gene.
Follicle stages
Comment
Phenotypes
Mutations
1 mutations
Species: sow
Mutation name: None
type: naturally occurring fertility: fertile Comment: Cloning, Sequence, and Association Analysis of Porcine OSAP Gene. Lei Y et al. Ovary-specific acidic protein (OSAP) is an important reproduction-related gene. In this study, we cloned the full-length cDNA sequence of porcine OSAP gene through the rapid amplification of cDNA ends method. The porcine OSAP gene encodes a protein of 238 amino acids which shares high homology with the OSAP of five species: rhesus monkey (72%), human (70%), cattle (68%), horse (68%), and dog (61%). This gene is structured in four exons and three introns as revealed by computer-assisted analysis. PCR-RFLP was established to detect the GU373669:c.854A>T substitution of porcine OSAP gene mRNA and association of this mutation with litter size traits was assessed in Large White (n?=?100) and Landrace (n?=?100) pig populations. Results demonstrated that this polymorphic locus was significantly associated with the litter size of all parities in Large White sows and Landrace sows (P?0.05). Therefore, OSAP gene could be a useful candidate gene in selection for increasing litter size in pigs. These data serve as a foundation for further insight into this novel porcine gene.