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

S Yonezawa, A Kimura, S Koshiba, S Masaki… - Biochemical and …, 2000 - Elsevier
S Yonezawa, A Kimura, S Koshiba, S Masaki, T Ono, A Hanai, S Sonta, T Kageyama…
Biochemical and biophysical research communications, 2000Elsevier
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 pleckstrin 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 …
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 pleckstrin 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 VIII–X of the spermatogenesis cycle, suggesting that myosin X is implicated in the supporting cells during the spermatid morphogenesis.
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