Literature DB >> 11079452

The CREM system in human spermatogenesis.

A Peri1, M Serio.   

Abstract

Spermatogenesis is a multi-step process, regulated by endocrine, paracrine and autocrine signals, through which immature germ cells differentiate into spermatozoa. The cAMP-dependent transcription factor CREM directs in the testis the expression of genes related to the structuring of mature spermatozoa. CREM gene expression originates different isoforms, which in turn can be divided into activators or repressors of gene expression. Whereas only CREM repressors are expressed in pre-meiotic germ cells in mice, a switch to the expression of the CREM activator tau occurs in post-meiotic germ cells. In addition, mice lacking CREM gene are infertile and present an arrest of germ cell maturation at the stage of round spermatid. We have demonstrated that CREM gene is expressed also in human germ cells and that a switch from the expression of repressors to activators is present in normospermic men. In particular, CREM tau mRNA is located in the cytoplasm of round spermatids. Conversely, in patients showing a testicular pattern of round spermatid maturation arrest only CREM repressors are expressed. Other reports have confirmed our data, supporting the hypothesis that CREM plays a role also in human spermatogenesis and that the absence of "the CREM switch" can be associated to spermatogenic arrest.

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Year:  2000        PMID: 11079452     DOI: 10.1007/BF03343779

Source DB:  PubMed          Journal:  J Endocrinol Invest        ISSN: 0391-4097            Impact factor:   4.256


  22 in total

Review 1.  Germ cell suicide: new insights into apoptosis during spermatogenesis.

Authors:  C G Print; K L Loveland
Journal:  Bioessays       Date:  2000-05       Impact factor: 4.345

Review 2.  Rhythmic transcription and autoregulatory loops: nuclear pacemaker CREM.

Authors:  M Lamas; E Lalli; N S Foulkes; P Sassone-Corsi
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1996

3.  Germ cell-specific cyclic adenosine 3',5'-monophosphate response element modulator expression in rodent and primate testis is maintained despite gonadotropin deficiency.

Authors:  R Behr; G F Weinbauer
Journal:  Endocrinology       Date:  1999-06       Impact factor: 4.736

4.  Expression of mRNA and protein of nucleoproteins during human spermiogenesis.

Authors:  K Steger; T Klonisch; K Gavenis; B Drabent; D Doenecke; M Bergmann
Journal:  Mol Hum Reprod       Date:  1998-10       Impact factor: 4.025

5.  Developmental switch of CREM function during spermatogenesis: from antagonist to activator.

Authors:  N S Foulkes; B Mellström; E Benusiglio; P Sassone-Corsi
Journal:  Nature       Date:  1992-01-02       Impact factor: 49.962

6.  Inducibility and negative autoregulation of CREM: an alternative promoter directs the expression of ICER, an early response repressor.

Authors:  C A Molina; N S Foulkes; E Lalli; P Sassone-Corsi
Journal:  Cell       Date:  1993-12-03       Impact factor: 41.582

Review 7.  Transcription factors responsive to cAMP.

Authors:  P Sassone-Corsi
Journal:  Annu Rev Cell Dev Biol       Date:  1995       Impact factor: 13.827

8.  Cyclic adenosine 3',5'-monophosphate-responsive element modulator gene expression in germ cells of normo- and oligoazoospermic men.

Authors:  A Peri; C Krausz; F Cioppi; S Granchi; G Forti; S Francavilla; M Serio
Journal:  J Clin Endocrinol Metab       Date:  1998-10       Impact factor: 5.958

9.  Induction of CREM activator proteins in spermatids: down-stream targets and implications for haploid germ cell differentiation.

Authors:  V Delmas; F van der Hoorn; B Mellström; B Jégou; P Sassone-Corsi
Journal:  Mol Endocrinol       Date:  1993-11

10.  Identification of a functional cyclic adenosine 3',5'-monophosphate response element in the 5'-flanking region of the gene for transition protein 1 (TP1), a basic chromosomal protein of mammalian spermatids.

Authors:  M K Kistler; P Sassone-Corsi; W S Kistler
Journal:  Biol Reprod       Date:  1994-12       Impact factor: 4.285

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  3 in total

1.  cAMP-response element modulator-tau activates a distinct promoter element for the expression of the phospholipid hydroperoxide/sperm nucleus glutathione peroxidase gene.

Authors:  Federica Tramer; Amedeo Vetere; Monica Martinelli; Federico Paroni; Eleonora Marsich; Carla Boitani; Gabriella Sandri; Enrico Panfili
Journal:  Biochem J       Date:  2004-10-01       Impact factor: 3.857

Review 2.  Alternative splicing: the pledge, the turn, and the prestige : The key role of alternative splicing in human biological systems.

Authors:  L M Gallego-Paez; M C Bordone; A C Leote; N Saraiva-Agostinho; M Ascensão-Ferreira; N L Barbosa-Morais
Journal:  Hum Genet       Date:  2017-04-03       Impact factor: 4.132

3.  Fhl5/Act, a CREM-binding transcriptional activator required for normal sperm maturation and morphology, is not essential for testicular gene expression.

Authors:  Aurélie Lardenois; Frédéric Chalmel; Philippe Demougin; Noora Kotaja; Paolo Sassone-Corsi; Michael Primig
Journal:  Reprod Biol Endocrinol       Date:  2009-11-24       Impact factor: 5.211

  3 in total

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