Different CREM-isoform gene expression between equine and human normal and impaired spermatogenesis

被引:16
作者
Blöcher, S
Behr, R
Weinbauer, GF
Bergmann, M
Steger, K
机构
[1] Univ Giessen, Inst Vet Anat Histol & Embryol, D-35392 Giessen, Germany
[2] Univ Essen Gesamthsch, Inst Anat Dev Biol, D-45122 Essen, Germany
[3] Covance Labs GmbH, D-48149 Munster, Germany
关键词
CREM; equine; human; infertility; spermatogenesis;
D O I
10.1016/S0093-691X(03)00142-0
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Histone-to-protamine exchange causes chromatin condensation ceasing gene expression in elongating spermatids. Gene expression of protamines is regulated by the transcription factor cAMP-responsive element modulator (CREM). Altered CREM expression results in male infertility, as shown by CREM-knock-out mice being sterile due to round spermatid maturation arrest and patients exhibiting round spermatid maturation arrest revealing a lack or substantial reduction of both CREM-mRNA and CREM-protein. Similar defects in histone-to-protamine exchange have been suggested in infertile stallions exhibiting enlarged sperm heads. The CREM-gene consists of 14 exons. Alternative exon splicing results in the production of both activator and repressor proteins. To further clarify the role of different CREM-isoforms for male infertility, the expression pattern of various CREM-isoforms during equine and human normal and impaired spermatogenesis was investigated by RT-PCR. Stallions with normal spermatogenesis expressed six activators and three repressors. In men three activators and seven different repressors were detected. In one stallion and patients with impaired spermatogenesis, only repressors were found. It is concluded that (i) stallion and man reveal a different CREM expression pattern, (ii) the expression of CREM activators is a prerequisite for normal spermatogenesis, and (iii) the lack of CREM activator expression results in male infertility. (C) 2003 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:1357 / 1369
页数:13
相关论文
共 31 条
[1]   ABERRANT PROTAMINE-1 PROTAMINE-2 RATIOS IN SPERM OF INFERTILE HUMAN MALES [J].
BALHORN, R ;
REED, S ;
TANPHAICHITR, N .
EXPERIENTIA, 1988, 44 (01) :52-55
[2]   CREM activator and repressor isoforms in human testis: sequence variations and inaccurate splicing during impaired spermatogenesis [J].
Behr, R ;
Weinbauer, GF .
MOLECULAR HUMAN REPRODUCTION, 2000, 6 (11) :967-972
[3]   Cloning and expression analysis of testis-specific cyclic 3′,5′-adenosine monophosphate-responsive element modulator activators in the nonhuman primate (Macaca fascicularis):: Comparison with other primate and rodent species [J].
Behr, R ;
Hunt, N ;
Ivell, R ;
Wessels, J ;
Weinbauer, GF .
BIOLOGY OF REPRODUCTION, 2000, 62 (05) :1344-1351
[4]   cCAMP response element modulator (CREM): an essential factor for spermatogenesis in primates? [J].
Behr, R ;
Weinbauer, GF .
INTERNATIONAL JOURNAL OF ANDROLOGY, 2001, 24 (03) :126-135
[5]  
BERGMANN M, 1998, ANDROLOGIE, P65
[6]   Severe impairment of spermatogenesis in mice lacking the CREM gene [J].
Blendy, JA ;
Kaestner, KH ;
Weinbauer, GF ;
Nieschlag, E ;
Schutz, G .
NATURE, 1996, 380 (6570) :162-165
[7]   Haploinsufficiency of protamine-1 or-2 causes infertility in mice [J].
Cho, C ;
Willis, WD ;
Goulding, EH ;
Haesook, JH ;
Choi, YC ;
Hecht, NB ;
Eddy, EM .
NATURE GENETICS, 2001, 28 (01) :82-86
[8]   Novel cyclic adenosine 3′,5′-monophosphate (cAMP) response element modulator θ isoforms expressed by two newly identified cAMP-responsive promoters active in the testis [J].
Daniel, PB ;
Rohrbach, L ;
Habener, JF .
ENDOCRINOLOGY, 2000, 141 (11) :3923-3930
[9]   CREM, a master-switch of the transcriptional cascade in male germ cells [J].
De Cesare, D ;
Fimia, GM ;
Sassone-Corsi, P .
JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION, 2000, 23 (09) :592-596
[10]   ALTERNATIVE USAGE OF INITIATION CODONS IN MESSENGER-RNA ENCODING THE CAMP-RESPONSIVE-ELEMENT MODULATOR GENERATES REGULATORS WITH OPPOSITE FUNCTIONS [J].
DELMAS, V ;
LAOIDE, BM ;
MASQUILIER, D ;
DEGROOT, RP ;
FOULKES, NS ;
SASSONECORSI, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (10) :4226-4230