Disruption of the murine PIASx gene results in reduced testis weight

被引:42
作者
Santti, H
Mikkonen, L
Anand, A
Hirvonen-Santti, S
Toppari, J
Panhuysen, M
Vauti, F
Perera, M
Corte, G
Wurst, W
Jänne, OA
Palvimo, JJ [1 ]
机构
[1] Univ Helsinki, Inst Biomed, Biomed Helsinki, FI-00014 Helsinki, Finland
[2] Univ Helsinki, Dept Clin Chem, FI-00014 Helsinki, Finland
[3] Univ Turku, Dept Physiol, FI-20520 Turku, Finland
[4] Univ Turku, Dept Pediat, FI-20520 Turku, Finland
[5] Univ Kuopio, Dept Med Biochem, FI-70211 Kuopio, Finland
[6] GSF, Inst Dev Genet, Natl Res Ctr Environm & Hlth, Neuherberg, Germany
[7] Univ Genoa, Lab Gene Transfer, Natl Inst Canc Res, Genoa, Italy
[8] Univ Genoa, DOBIG, Genoa, Italy
关键词
D O I
10.1677/jme.1.01666
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
PIASx belongs to the PIAS protein family, the members of which modulate activities of several transcription factors and act as E3 ligases in the sumoylation pathway. The PIASx gene is highly expressed in testis, suggesting a role in spermatogenesis. To investigate the function of PIASx in vivo, we have disrupted the PIASx gene in mice. Interestingly, the knockout mice were viable and fertile. Despite the normal fertility, the testis weight of the mutant animals was reduced and their number of apoptotic testicular cells was increased. Also, the sperm count of mutant mice tended to be reduced, but the quality of their sperm cells was normal. No significant changes were observed in the serum levels of LH and FSH or in the intratesticular testosterone concentration between the knockout animals and their wild-type littermates. Compensatory increases in other PIAS protein mRNAs were not observed in the knockout mice. These results imply that PIASx is required quantitatively rather than qualitatively for normal spermatogenesis.
引用
收藏
页码:645 / 654
页数:10
相关论文
共 58 条
  • [1] Augmenter of liver regeneration enhances the success rate of fetal pancreas transplantation in rodents
    Adams, GA
    Maestri, M
    Squiers, EC
    Alfrey, EJ
    Starzl, TE
    Dafoe, DC
    [J]. TRANSPLANTATION, 1998, 65 (01) : 32 - 36
  • [2] A Drosophila PIAS homologue negatively regulates stat92E
    Betz, A
    Lampen, N
    Martinek, S
    Young, MW
    Darnell, JE
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (17) : 9563 - 9568
  • [3] BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
  • [4] Specific inhibition of Stat3 signal transduction by PIAS3
    Chung, CD
    Liao, JY
    Liu, B
    Rao, XP
    Jay, P
    Berta, P
    Shuai, K
    [J]. SCIENCE, 1997, 278 (5344) : 1803 - 1805
  • [5] Mouse models of male infertility
    Cooke, HJ
    Saunders, PTK
    [J]. NATURE REVIEWS GENETICS, 2002, 3 (10) : 790 - 801
  • [6] SUMO-1 modification of IκBα inhibits NF-κB activation
    Desterro, JMP
    Rodriguez, MS
    Hay, RT
    [J]. MOLECULAR CELL, 1998, 2 (02) : 233 - 239
  • [7] Activation of p53 by conjugation to the ubiquitin-like protein SUMO-1
    Gostissa, M
    Hengstermann, A
    Fogal, V
    Sandy, P
    Schwarz, SE
    Scheffner, M
    Del Sal, G
    [J]. EMBO JOURNAL, 1999, 18 (22) : 6462 - 6471
  • [8] Distinct effects of PIAS proteins on androgen-mediated gene activation in prostate cancer cells
    Gross, M
    Liu, B
    Tan, JA
    French, FS
    Carey, M
    Shuai, K
    [J]. ONCOGENE, 2001, 20 (29) : 3880 - 3887
  • [9] A SUPERSENSITIVE IMMUNOFLUOROMETRIC ASSAY FOR RAT LUTEINIZING-HORMONE
    HAAVISTO, AM
    PETTERSSON, K
    BERGENDAHL, M
    PERHEENTUPA, A
    ROSER, JF
    HUHTANIEMI, I
    [J]. ENDOCRINOLOGY, 1993, 132 (04) : 1687 - 1691
  • [10] CLONING AND SEQUENCE-ANALYSIS OF THE RAT AUGMENTOR OF LIVER-REGENERATION (ALR) GENE - EXPRESSION OF BIOLOGICALLY-ACTIVE RECOMBINANT ALR AND DEMONSTRATION OF TISSUE DISTRIBUTION
    HAGIYA, M
    FRANCAVILLA, A
    POLIMENO, L
    IHARA, I
    SAKAI, H
    SEKI, T
    SHIMONISHI, M
    PORTER, KA
    STARZL, TE
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (17) : 8142 - 8146