## Abstract We have chosen three species (__Sparus aurata, Dicentrarchus labrax__, and __Monodonta turbinata__) that represent different transition patterns in the composition and structure of spermiogenic nuclei. The transition patterns of these species are representative of spermiogenesis in a la
Transition nuclear proteins are required for normal chromatin condensation and functional sperm development
✍ Scribed by Ming Zhao; Cynthia R. Shirley; Shotaro Hayashi; Ludovic Marcon; Bhagyalaxmi Mohapatra; Ryota Suganuma; Richard R. Behringer; Guylain Boissonneault; Ryuzo Yanagimachi; Marvin L. Meistrich
- Book ID
- 102843587
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 756 KB
- Volume
- 38
- Category
- Article
- ISSN
- 1526-954X
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✦ Synopsis
Abstract
Summary: The histone‐to‐protamine transition is important in the formation of spermatozoa. In mammals this involves two steps: replacement of histones by transition nuclear proteins (TPs) and replacement of TPs by protamines. To determine the functions of the TPs and their importance for sperm development, we generated mice lacking both TPs, since mice lacking only TP1 or TP2 were fertile. Our results indicated that TP1 and TP2 had partially complemented each other. In mice lacking both TPs, nuclear shaping, transcriptional repression, histone displacement, and protamine deposition proceeded relatively normally, but chromatin condensation was irregular in all spermatids, many late spermatids showed DNA breaks, and protamine 2 was not posttranslationally processed. Nevertheless, genomic integrity was maintained in mature spermatids, since efficient fertilization and production of offspring were achieved by intracytoplasmic sperm injection. However, many mature spermatids were retained in the testis, epididymal spermatozoa were drastically reduced in number and were highly abnormal, and the mice were sterile. Most epididymal spermatozoa were incapable of fertilization even using intracytoplasmic sperm injection. Thus, in mammals TPs are required for normal chromatin condensation, for reducing the number of DNA breaks, and for preventing the formation of secondary defects in spermatozoa, eventual loss of genomic integrity, and sterility. genesis 38:200–213, 2004. © 2004 Wiley‐Liss, Inc.
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