Krämer A, Legrain P, Mulhauser F, Gröning K, Brosi R, Bilbe G
Départment de Biologie Cellulaire, Univesité de Genève, Switzerland.
Nucleic Acids Res. 1994 Dec 11;22(24):5223-8. doi: 10.1093/nar/22.24.5223.
A cDNA encoding the 60 kDa subunit of mammalian splicing factor SF3a has been isolated. The deduced protein sequence reveals a 30% identity to the PRP9 splicing protein of the yeast S.cerevisiae. The highest homology is present in a zinc finger-like region in the C-terminal domain of both proteins. The PRP9 zinc finger-like motif has been replaced by the equivalent region of mammalian SF3a60. The chimeric protein rescues the temperature-sensitive phenotype of the prp9-1 mutant strain demonstrating that not only the structure but also the function of this domain has been conserved during evolution.
已分离出编码哺乳动物剪接因子SF3a 60 kDa亚基的cDNA。推导的蛋白质序列显示与酿酒酵母的PRP9剪接蛋白有30%的同一性。最高同源性存在于两种蛋白质C端结构域的锌指样区域。PRP9锌指样基序已被哺乳动物SF3a60的等效区域取代。嵌合蛋白挽救了prp9-1突变菌株的温度敏感表型,表明该结构域不仅结构而且功能在进化过程中都得到了保留。