Mouse myosin X:: Molecular architecture and tissue expression as revealed by northern blot and in situ hybridization analyses

被引:24
作者
Yonezawa, S [1 ]
Kimura, A
Koshiba, S
Masaki, S
Ono, T
Hanai, A
Sonta, S
Kageyama, T
Takahashi, T
Moriyama, A
机构
[1] Aichi Human Serv Ctr, Inst Dev Res, Dept Dev Biol, Kasugai, Aichi 4800392, Japan
[2] Hokkaido Univ, Grad Sch Sci, Div Biol Sci, Sapporo, Hokkaido 0600810, Japan
[3] RIKEN, Inst Phys & Chem Res, Wako, Saitama 3510198, Japan
[4] Kyoto Univ, Primate Res Inst, Inuyama, Aichi 4848506, Japan
[5] Nagoya City Univ, Inst Nat Sci, Nagoya, Aichi 4670802, Japan
关键词
unconventional myosin; myosin X; PH domain; MyTH4; domain; talin-like domain; testis; Sertoli cell; Myo10;
D O I
10.1006/bbrc.2000.2669
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The structure of the coding region of mouse myosin X cDNA was determined. The predicted protein sequence indicated an approximately 240 kDa molecular mass with 2062 amino acids. When aligned with the structure predicted for calf myosin X (GenBank Accession No. U55042), extremely highly conserved pleck-strin homology domains and a myosin tail homology 4 domain were apparent in the tail region, suggesting their importance for myosin X's function. Northern blot analysis revealed the existence of a myosin X mRNA, 8.7 kb in size, in various mouse tissues, while a similar size of human type myosin X mRNA was recognized mainly in the testis. In addition to the adult-type transcripts in mice, a smaller embryo-specific mRNA, 4.8 kb in size, was identified in early to late embryonic stages, suggesting the presence of a shorter myosin X isoform in mouse embryos. In situ hybridization experiments with mouse testis revealed that myosin X mRNA was restricted to Sertoli cells at stages Vm-X of the spermatogenesis cycle, suggesting that myosin X is implicated in the supporting cells during the spermatid morphogenesis. (C) 2000 Academic Press.
引用
收藏
页码:526 / 533
页数:8
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