Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractHS-SPME-GC-MS technique for FFA and hexanal analysis in different cheese packaging in the course of long term storage    Next AbstractEvaluation of blood assays for detection of Mycobacterium bovis in white-tailed deer (Odocoileus virginianus) in Michigan »

Mol Reprod Dev


Title:Boar proacrosin expressed in spermatids of transgenic mice does not reach the acrosome and disrupts spermatogenesis
Author(s):O'Brien DA; Welch JE; Goulding EH; Taylor AA; Baba T; Hecht NB; Eddy EM;
Address:"Department of Pediatrics, University of North Carolina at Chapel Hill 27599-7500, USA"
Journal Title:Mol Reprod Dev
Year:1996
Volume:43
Issue:2
Page Number:236 - 247
DOI: 10.1002/(SICI)1098-2795(199602)43:2<236::AID-MRD13>3.0.CO;2-1
ISSN/ISBN:1040-452X (Print) 1040-452X (Linking)
Abstract:"Transgenic mice that express boar proacrosin were produced to examine mechanisms for targeting hydrolytic enzymes to the acrosome. A 2.3 kb transgene was constructed by ligating the cDNA for boar preproacrosin with the mouse protamine 2 promoter region. Six founder mice that incorporated the transgene were identified by polymerase chain reaction and Southern blot analysis. Northern blots indicated that the two male founders (Ac.2 and Ac.5) and male progeny from three female founders (Ac.3, Ac.4, Ac.6) expressed the transgene mRNA in testis, but not in somatic tissues. In these transgenic animals boar proacrosin was detected by immunohistochemistry in condensing spermatids, but was not localized in the acrosome. This acrosomal targeting defect of the transgene product may result from its delayed expression during the later steps of haploid differentiation. Furthermore, both male founders and all Ac.4 and Ac.6 males were infertile, as determined by multiple matings for at least 2 months. Ac.3 males were either infertile or rarely transmitted the transgene to their offspring. The infertile males mated, produced copulatory plugs, and had seminal vesicle weights and testosterone levels within the normal range. However, they produced significantly fewer spermatozoa and had lower testis weights than controls. Although the mitotic and meiotic phases of spermatogenesis appeared normal by histological criteria, condensing spermatids were missing from most tubules, and multinucleated cells were present in the lumen of seminiferous tubules and in the epididymis. We hypothesize that boar proacrosin which fails to reach the acrosome is activated in these transgenic mice, and that its proteolytic activity disrupts spermatogenesis during spermatid formation"
Keywords:"Acrosin/genetics/*metabolism Acrosome/*metabolism Animals Enzyme Precursors/genetics/*metabolism Gene Expression Regulation, Developmental Male Mice Mice, Transgenic Spermatids/*metabolism *Spermatogenesis/genetics;"
Notes:"MedlineO'Brien, D A Welch, J E Goulding, E H Taylor, A A Jr Baba, T Hecht, N B Eddy, E M eng CA16086/CA/NCI NIH HHS/ HD18968/HD/NICHD NIH HHS/ HD26485/HD/NICHD NIH HHS/ Research Support, U.S. Gov't, P.H.S. 1996/02/01 Mol Reprod Dev. 1996 Feb; 43(2):236-47. doi: 10.1002/(SICI)1098-2795(199602)43:2<236::AID-MRD13>3.0.CO; 2-1"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 25-11-2024