Sperm equatorial segment protein 1, SPESP1, is required for fully fertile sperm in mouse

被引:86
作者
Fujihara, Yoshitaka [1 ]
Murakami, Masao [1 ]
Inoue, Naokazu [1 ]
Satouh, Yuhkoh [1 ]
Kaseda, Kazuhiro [1 ]
Ikawa, Masahito [1 ]
Okabe, Masaru [1 ]
机构
[1] Osaka Univ, Microbial Dis Res Inst, Suita, Osaka 5650871, Japan
关键词
Equatorial segment; Fertilization; Knockout mouse; Sperm-egg fusion; EGG PLASMA-MEMBRANE; MONOCLONAL-ANTIBODY; CD9-DEFICIENT MICE; IN-VIVO; FUSION; FERTILIZATION; DEFICIENT; CALMEGIN; ADAM3; MATURATION;
D O I
10.1242/jcs.067363
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mammalian fertilization is a multistep process that culminates in the fusion of the sperm and egg plasma membrane. It is widely accepted that the equatorial segment of the acrosome-reacted sperm is important in initiating fusion with the egg plasma membrane during fertilization. There are various proteins known to be distributed only in the equatorial segment of sperm. The role of these proteins must be clarified to understand the membrane fusion process. We produced a mouse line that lacked SPESP1 (sperm equatorial segment protein 1) and analyzed the fertilizing ability of the sperm. The average number of pups that were fathered by Spesp1(+/-) and Spesp1(-/-) males was significantly lower than that of wild-type fathers. In these mouse lines, fewer sperm were found to migrate into oviducts and fewer eggs were fertilized. The Spesp1(+/-) and Spesp1(-/-) sperm showed a lower fusing ability compared with the wildtype sperm. The disruption of Spesp1 was shown to cause an aberrant distribution of various sperm proteins. Moreover, scanning electron microscopy revealed that the membrane in the equatorial segment area, which usually forms an acrosomal sheath, disappears after acrosome reaction in Spesp1-deficient mice. It was demonstrated that SPESP1 is necessary to produce the fully 'fusion competent' sperm.
引用
收藏
页码:1531 / 1536
页数:6
相关论文
共 29 条
[1]  
BORDIER C, 1981, J BIOL CHEM, V256, P1604
[2]   Fertilization defects in sperm from mice lacking fertilinβ [J].
Cho, CH ;
Bunch, DO ;
Faure, JE ;
Goulding, EH ;
Eddy, EM ;
Primakoff, P ;
Myles, DG .
SCIENCE, 1998, 281 (5384) :1857-1859
[3]   Transgenic Mouse Sperm that Have Green Acrosome and Red Mitochondria Allow Visualization of Sperm and Their Acrosome Reaction in Vivo [J].
Hasuwa, Hidetoshi ;
Muro, Yuko ;
Ikawa, Masahito ;
Kato, Noriko ;
Tsujimoto, Yoshihide ;
Okabe, Masaru .
EXPERIMENTAL ANIMALS, 2010, 59 (01) :105-107
[4]   A null mutation in basigin, an immunoglobulin superfamily member, indicates its important roles in peri-implantation development and spermatogenesis [J].
Igakura, T ;
Kadomatsu, K ;
Kaname, T ;
Muramatsu, H ;
Fan, QW ;
Miyauchi, T ;
Toyama, Y ;
Kuno, N ;
Yuasa, S ;
Takahashi, M ;
Senda, T ;
Taguchi, O ;
Yamamura, K ;
Arimura, K ;
Muramatsu, T .
DEVELOPMENTAL BIOLOGY, 1998, 194 (02) :152-165
[5]   The putative chaperone calmegin is required for sperm fertility [J].
Ikawa, M ;
Wada, I ;
Kominami, K ;
Watanabe, D ;
Toshimori, K ;
Nishimune, Y ;
Okabe, M .
NATURE, 1997, 387 (6633) :607-611
[6]   The immunoglobulin superfamily protein Izumo is required for sperm to fuse with eggs [J].
Inoue, N ;
Ikawa, M ;
Isotani, A ;
Okabe, M .
NATURE, 2005, 434 (7030) :234-238
[7]   Putative sperm fusion protein IZUMO and the role of N-glycosylation [J].
Inoue, Naokazu ;
Ikawa, Masahito ;
Okabe, Masaru .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2008, 377 (03) :910-914
[8]   The gamete fusion process is defective in eggs of Cd9-deficient mice [J].
Kaji, K ;
Oda, S ;
Shikano, T ;
Ohnuki, T ;
Uematsu, Y ;
Sakagami, J ;
Tada, N ;
Miyazaki, S ;
Kudo, A .
NATURE GENETICS, 2000, 24 (03) :279-282
[9]   FLOW CYTOMETRIC ANALYSIS OF MOUSE SPERM USING MONOCLONAL ANTI-SPERM ANTIBODY OBF13 [J].
KAWAI, Y ;
HAMA, T ;
MAYUMI, T ;
OKABE, M ;
MATZNO, S ;
KOHAMA, Y ;
MIMURA, T .
JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 1989, 16 (01) :71-&
[10]   Preparation, isolation and characterization of stage-specific spermatogenic cells for cellular and molecular analysis [J].
Kotaja, N ;
Kimmins, S ;
Brancorsini, S ;
Hentsch, D ;
Vonesch, JL ;
Davidson, I ;
Parvinen, M ;
Sassone-Corsi, P .
NATURE METHODS, 2004, 1 (03) :249-254