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Endocrine Disruptor Research Initiative
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EDRI Federal Project Inventory:
Androgenic Regulation of Epididymal Sperm Binding Proteins: Role of RNA-Binding Proteins



  1. Sponsor Organization: NATIONAL SCIENCE FOUNDATION

  2. Project Title: ANDROGENIC REGULATION OF EPIDIDYMAL SPERM BINDING PROTEINS: ROLE OF RNA-BINDING PROTEINS

  3. Project Focus: HUMAN HEALTH EFFECTS

  4. Description: In all male mammalian species, including man, spermatozoa that leave the testis areinfertile and immobile. The acquisition of fertilizing capacity and motility byspermatozoa occurs in an organ called the epididymis and the overall process is oftenreferred to as "sperm maturation". It is now well accepted in reproductive biology andbiochemistry that spermatozoan maturation is mediated by proteins and glycoproteinscalled fertility antigens. These fertility antigens are secreted by the epididymis underthe control of the male hormone, testosterone. Using the rat as an experimental model,Dr. Hall has identified a key fertility antigen that is secreted by the epididymis and bindsto the sperm plasma membrane. This sperm plasma membrane antigen which issynthesized by the epididymis plays a key physiological role in plasma membranechanges on the surface spermatozoa that accompany the development of fertilizingcapacity and motility in mammals. An initial step toward elucidating the basic causes ofmale infertility or developing compounds as potential male contraceptives is tounderstand how these fertility antigens are regulated in the mammalian epididymis.Thus, the broad, long-term objective of the present study is to provide a basicunderstanding of how fertility antigens are regulated. A working model for theandrogen- dependent synthesis of this fertility antigen is proposed in this study. Aunique feature of the model is that the synthesis of this fertility antigen may beregulated at the level of its own messenger RNA (mRNA). He further hypothesizes thatthe rate at which this fertility antigen is synthesized in cells of the epididymis iscontrolled by proteins that bind to its mRNA. If this hypothesis proves correct, it may bepossible in the near future to develop a compound that can selectively block(contraceptive) or enhance (conception) the synthesis of the fertility antigen.

  5. References:

  6. Category: MODELS

  7. Subcategory: BASIC RESEARCH

  8. Keywords for Experimental System/Species: MAMMALIAN, IN VIVO, IN VITRO, LABORATORY STUDY

  9. Keywords for Experimental Endpoints: IMMUNOLOGICAL, REPRODUCTIVE, MALE, HORMONE RECEPTORS, BREEDING BEHAVIOR,

  10. Chemical Agents: Sex Steroids

  11. Performing Institution: North Carolina State University

  12. Contact: Joseph C Hall, P.O. BOX 7003, Raleigh, NC 27650-5067 919 737-2011


 

 
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