Fertilization defects in sperm from mice lacking fertilin beta.
ABSTRACT Fertilin, a member of the ADAM family, is found on the plasma membrane of mammalian sperm. Sperm from mice lacking fertilin beta were shown to be deficient in sperm-egg membrane adhesion, sperm-egg fusion, migration from the uterus into the oviduct, and binding to the egg zona pellucida. Egg activation was unaffected. The results are consistent with a direct role of fertilin in sperm-egg plasma membrane interaction. Fertilin could also have a direct role in sperm-zona binding or oviduct migration; alternatively, the effects on these functions could result from the absence of fertilin activity during spermatogenesis.
SourceAvailable from: Qun Wang[Show abstract] [Hide abstract]
ABSTRACT: The ADAM (a disintegrin and metalloprotease) family plays an important role in sperm and egg fusion, development, inflammation, adhesion and migration. ADAM10 and ADAM17 are involved in the spermatogenesis. To better understand the role of ADAM10 and ADAM17 in the Chinese mitten crab, Eriocheir sinensis, the full-length cDNAs of ADAM10 and ADAM17 were cloned, and named Es-ADAM10 and Es-ADAM17, respectively. Sequence and structural analysis showed that Es-ADAM10 and Es-ADAM17 have the typical structure of the ADAM family. Quantitative real-time reverse transcription polymerase chain reaction analysis showed that Es-ADAM10 and Es-ADAM17 mRNAs were distributed in the heart, hepatopancreas, intestines, brain, muscle, thoracic ganglia, hemolymph, stomach, testis, ovary, gill and accessory gland. Both mRNAs were highly expressed in the muscles, and relatively high in the testis, ovary and accessory gland. In addition, the Es-ADAM17 mRNA level was detected in every stage of testis development, being relatively high from July to September, the lowest during October and November, increasing from December to January, and reached a peak in January. By contrast, the expression of Es-ADAM10 mRNA was constant during testis development. Immunofluorescence further showed that Es-ADAM10 and Es-ADAM17 proteins were present in the cytoplasm and cytomembrane of spermatocytes, and both detected in the sperm. Furthermore, etoposide induced upregulation of Es-ADAM17 and Es-ADAM10 at both the mRNA and protein levels. This study first showed that Es-ADAM10 and Es-ADAM17 were also involved in the spermatogenesis and mainly participated in the later germ cell apoptosis in E. sinensis. Copyright © 2015. Published by Elsevier B.V.Gene 02/2015; 562(1). DOI:10.1016/j.gene.2015.02.060 · 2.08 Impact Factor
[Show abstract] [Hide abstract]
ABSTRACT: Most male mammals produce far more spermatozoa on a daily basis than is strictly necessary for reproduction and females have evolved mechanisms that prevent all but a small minority from reaching the vicinity of their oocytes. One potential explanation for the stringent selection is that females have developed these mechanisms as a way of avoiding polyspermy as well as exercising post-copulatory choice over the characteristics of the fertilizing spermatozoon. Relatively little is known about how these processes would operate but here we use evidence from biochemical, molecular and genetic studies of sperm transport in support of a hypothesis proposing that the female reproductive tract can read and interpret a spermatozoon's "molecular passport" or genetic signature. Such a signature would permit only a highly selected sperm population to reach and fertilize the oocyte. Moreover, the selection criteria might not only be concerned with successful fertilizing ability, but could also be tailored to suit the genetic qualities of individual females. © The Author 2015. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: firstname.lastname@example.org.Molecular Human Reproduction 03/2015; DOI:10.1093/molehr/gav012 · 3.48 Impact Factor
[Show abstract] [Hide abstract]
ABSTRACT: The objective of the present study is to provide a comprehensive in silco sequence analyses of sperm-surface ADAM genes using the curated and nonredundant RefSeq database. 36 complete refseq CDS (coding sequence) of 9 members of ADAM gene family namely ADAM1,2,3,4,5,6,18,24 and 32 were obtained to investigate its evolution and differentiation within and among species. Among the 9 sperm-surface genes ADAM1 has the longest CDS length, the highest GC% and largest variation in base composition. Measurement of polymorphism and genetic diversity (e.g. Number of haplotypes, nucleotide diversity (π) and average number of nucleotide diversity) varied greatly among the sperm-surface ADAM genes. These large variations are evidence for the effect of selection pressure on these genes. The phylogenetic analysis displayed clearly the resolved relationship of sperm-surface ADAM genes and most of bootstrap support were high. Sperm-surface ADAM genes were classified into 6 clades where, ADAM1,2,3,4,5,6,18,24 and ADAM32 of B.taurus and H. sapiens categorizing to one large lineage where ADAM32 of R. norvegicus and M. musculus belonging to another separate lineage. In conclusion, the in silico analysis of the 9 sperm-surface ADAM genes showed a great deal of variation among and within this genes indicating the presence of localized signals of selection pressure on these genes. Moreover, ADAM1,4,6 and 24 have no human orthologues. More importantly, our results suggested that ADAM1,2,3,4,5,6, 18,24 and ADAM32 of B.taurus and H. sapiens were descendent form one ancient ancestor, where ADAM32 of R. norvegicus and M. musculus have another ancestor.