Isolation and characterization of goldfish Y box protein, a germ-cell-specific RNA-binding protein

被引:14
作者
Katsu, Y
Yamashita, M
Nagahama, Y
机构
[1] NATL INST BASIC BIOL, REPROD BIOL LAB, OKAZAKI, AICHI 444, JAPAN
[2] HOKKAIDO UNIV, GRAD SCH SCI, LAB MOL & CELLULAR INTERACT, DIV BIOL SCI, SAPPORO, HOKKAIDO 060, JAPAN
来源
EUROPEAN JOURNAL OF BIOCHEMISTRY | 1997年 / 249卷 / 03期
关键词
goldfish; oocyte maturation cyclin B; Y box protein; RNA-binding protein;
D O I
10.1111/j.1432-1033.1997.00854.x
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
Cyclin B is a regulatory subunit of maturation-promoting factor. In goldfish (Carassius auratus) oocytes, cyclin B is synthesized de novo after stimulation by 17 alpha,20 beta-dihydroxy-4-pregnen-3-one (maturation-inducing hormone). In this study, we examined goldfish oocyte proteins bound to cyclin B mRNA. Using oligo(dT)-cellulose affinity chromatography and northwestern blotting analysis, we identified a 54-kDa cyclin B mRNA-binding protein (p54). Southwestern blotting analysis showed the binding of p54 to the Y box DNA element (CTGATTGGCCAA), suggesting that p54 is a Y box protein in goldfish. We isolated two cDNA clones, GFYP1 and GFYP2, the latter of which encodes a germ-cell-specific Y box protein. An antibody against a GFYP2 protein recognized p54, suggesting that p54 is identical or highly similar to GFYP2 protein. This is also supported by the finding that a recombinant GFYP2 expressed in bacteria bound to both the Y box DNA element and the goldfish cyclin B mRNA synthesized in vitro. These results suggest that p54 is a germ-cell-specific Y box protein and is a potential masking protein of cyclin B mRNA in goldfish oocytes.
引用
收藏
页码:854 / 861
页数:8
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