Comparison of the effect of two freeze-thawing curves for porcine semen. Preliminary results

Results obtained in fertility and litter size using frozen-thawed porcine semen are far from those obtained with natural service or artificial insemination of cooled semen. The objective of this study was to evaluate freeze-thawing of porcine semen comparing the traditional slow method to a rapid curve of temperature descent, using two cryoprotectants. Six males of proven fertility (n=6, r=2) were used. Semen was obtained using the gloved-hand technique and was transported to the laboratory at 17 ºC diluted in Androstar® plus. Samples were centrifuged 15 minutes at 800 g and re-diluted in: a) 5% dimethylformamide, 11% lactose, 20% egg yolk, 0.5% Equex or b) 3% glycerol, 11% lactose, 20% egg yolk, 0.5% Equex. The semen was frozen in 0.5 ml straws up to a final concentration of 300 millions sperm /ml using either a modified slow traditional Westendorff curve or a rapid curve. In both cases thawing was carried out at 37 ºC during 1 minute. Kinetic motility parameters were evaluated using a CASA system (ISAS v1, Proiser®, Spain). Sperm viability and acrosome status were evaluated using the FITC-PNA/PI stain. The results were analyzed using a factorial design (analysis ofvariance) with two factors, with two levels for each one and using the male as a blocking factor. No interaction was observed between the parameters. No significant differences (p> 0.05) were observed between curves or between cryoprotectants neither in any of the kinetic motility parameters evaluated nor in sperm viability and acrosome status. No significant differences (p> 0.05) were observed between curves or between cryoprotectants in sperm morphology in thawed porcine semen. Taking into account the results obtained, the rapid curve would be the practical choice as it is, faster and more manageable for fieldwork in any pig farm

New mouse genetic models for human contraceptive development.

Genetic strategies for the post-genomic sequence age will be designed to provide information about gene function in a myriad of physiological processes. Here an ENU mutagenesis program (http://reprogenomics.jax.org) is described that is generating a large resource of mutant mouse models of infertility; male and female mutants with defects in a wide range of reproductive processes are being recovered. Identification of the genes responsible for these defects, and the pathways in which these genes function, will advance the fields of reproduction research and medicine. Importantly, this program has potential to reveal novel human contraceptive targets

Phenotypic variability and abnormal type I collagen unstable at body temperature in a family with mild dominant osteogenesis imperfecta.

Autosomal dominant inheritance of a mild form of osteogenesis imperfecta (osteogenesis imperfecta type I) with different phenotypic expression was found in a family. Phenotypic expression was different for the affected mother and son, in the presence of the same biochemical results. Dermal fibroblast cultures synthesized normal and mutant type I collagen alpha chains. Collagen heterotrimers containing abnormal chains were overmodified along the entire triple helical domain and showed an unusually low denaturation temperature, so far found only in lethal cases. The mild phenotype in the family is probably due to the fact that abnormal type I collagen molecules are more likely to be degraded than utilized in the extracellular matrix

MARF1 regulates essential oogenic processes in mice.

Development of fertilization-competent oocytes depends on integrated processes controlling meiosis, cytoplasmic development, and maintenance of genomic integrity. We show that meiosis arrest female 1 (MARF1) is required for these processes in mammalian oocytes. Mutations of Marf1 cause female infertility characterized by up-regulation of a cohort of transcripts, increased retrotransposon expression, defective cytoplasmic maturation, and meiotic arrest. Up-regulation of protein phosphatase 2 catalytic subunit (PPP2CB) is key to the meiotic arrest phenotype. Moreover, Iap and Line1 retrotransposon messenger RNAs are also up-regulated, and, concomitantly, DNA double-strand breaks are elevated in mutant oocytes. Therefore MARF1, by suppressing levels of specific transcripts, is an essential regulator of important oogenic processes leading to female fertility and the development of healthy offspring

AKAP9 is essential for spermatogenesis and sertoli cell maturation in mice.

Mammalian male fertility relies on complex inter- and intracellular signaling during spermatogenesis. Here we describe three alleles of the widely expressed A-kinase anchoring protein 9 (Akap9) gene, all of which cause gametogenic failure and infertility in the absence of marked somatic phenotypes. Akap9 disruption does not affect spindle nucleation or progression of prophase I of meiosis but does inhibit maturation of Sertoli cells, which continue to express the immaturity markers anti-Mullerian hormone and thyroid hormone receptor alpha in adults and fail to express the maturation marker p27(Kip1). Furthermore, gap and tight junctions essential for blood-testis barrier (BTB) organization are disrupted. Connexin43 (Cx43) and zona occludens-1 are improperly localized in Akap9 mutant testes, and Cx43 fails to compartmentalize germ cells near the BTB. These results identify and support a novel reproductive tissue-specific role for Akap9 in the coordinated regulation of Sertoli cells in the testis. Genetics 2013 Jun; 194(2):447-57

Toward the genetics of mammalian reproduction: induction and mapping of gametogenesis mutants in mice.

The genetic control of mammalian gametogenesis is inadequately characterized because of a lack of mutations causing infertility. To further the discovery of genes required for mammalian gametogenesis, phenotype-driven screens were performed in mice using random chemical mutagenesis of whole animals and embryonic stem cells. Eleven initial mutations are reported here that affect proliferation of germ cells, meiosis, spermiogenesis, and spermiation. Nine of the mutations have been mapped genetically. These preliminary studies provide baselines for estimating the number of genes required for gametogenesis and offer guidance in conducting new genetic screens that will accelerate and optimize mutant discovery. This report demonstrates the efficacy and expediency of mutagenesis to identify new genes required for mammalian gamete development