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
  • [51] Modification with SUMO - A role in transcriptional regulation
    Verger, A
    Perdomo, J
    Crossley, M
    [J]. EMBO REPORTS, 2003, 4 (02) : 137 - 142
  • [52] Increased K+ efflux and apoptosis induced by the potassium channel modulatory protein KChAP/PIAS3β in prostate cancer cells
    Wible, BA
    Wang, LM
    Kuryshev, YA
    Basu, A
    Haldar, S
    Brown, AM
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (20) : 17852 - 17862
  • [53] Establishment of a gene-trap sequence tag library to generate mutant mice from embryonic stem cells
    Wiles, MV
    Vauti, F
    Otte, J
    Füchtbauer, EM
    Ruiz, P
    Füchtbauer, A
    Arnold, HH
    Lehrach, H
    Metz, T
    von Melchner, H
    Wurstz, W
    [J]. NATURE GENETICS, 2000, 24 (01) : 13 - 14
  • [54] The LightCycler(TM) a microvolume multisample fluorimeter with rapid temperature control
    Wittwer, CT
    Ririe, KM
    Andrew, RV
    David, DA
    Gundry, RA
    Balis, UJ
    [J]. BIOTECHNIQUES, 1997, 22 (01) : 176 - 181
  • [55] Protein inhibitor of activated STAT y (PIASy) and a splice variant lacking exon 6 enhance sumoylation but are not essential for embryogenesis and adult life
    Wong, KA
    Kim, R
    Christofk, H
    Gao, J
    Lawson, G
    Wu, H
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (12) : 5577 - 5586
  • [56] Real-time homogeneous assay of rapid cycle polymerase chain reaction product for identification of Leptonema illini
    Woo, THS
    Patel, BKC
    Cinco, M
    Smythe, LD
    Symonds, ML
    Norris, MA
    Dohnt, MF
    [J]. ANALYTICAL BIOCHEMISTRY, 1998, 259 (01) : 112 - 117
  • [57] The crystal structure of augmenter of liver regeneration: A mammalian FAD-dependent sulfhydryl oxidase
    Wu, CK
    Dailey, TA
    Dailey, HA
    Wang, BC
    Rose, JP
    [J]. PROTEIN SCIENCE, 2003, 12 (05) : 1109 - 1118
  • [58] Expression of the E3 SUMO-1 ligases PIASx and PIAS1 during spermatogenesis in the rat
    Yan, W
    Santti, H
    Jänne, OA
    Palvimo, JJ
    Toppari, J
    [J]. GENE EXPRESSION PATTERNS, 2003, 3 (03) : 301 - 308