SIGNAL SEQUENCE FOR GENERATION OF MESSENGER-RNA 3' END IN THE SACCHAROMYCES-CEREVISIAE GAL7 GENE

被引:54
作者
ABE, A
HIRAOKA, Y
FUKASAWA, T
机构
[1] KEIO UNIV,SCH MED,DEPT MICROBIOL,35 SHINANOMACHI,SHIJUKU K,TOKYO 160,JAPAN
[2] KITASATO INST,MINATO KU,TOKYO 108,JAPAN
[3] KEIO UNIV,MOLEC GENET LAB,SHINJUKU KU,TOKYO 160,JAPAN
关键词
deletion analysis; in vitro processing; polyadenylation site; yeast;
D O I
10.1002/j.1460-2075.1990.tb07581.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
We have identified a signal sequence (designated core signal) necessary to specify formation of mRNA 3' end of the GAL7 gene in Saccharomyces cerevisiae within a DNA segment 26 bp long. The sequence was located 4-5 nucleotides upstream from the 3' end, i.e. the polyadenylation site, of the GAL7 mRNA. Replacement of a DNA segment encompassing the polyadenylation site with a pBR322 DNA, leaving the core signal intact, resulted in alteration of the mRNA 3' end by several nucleotides, suggesting the existence of an additional signal (designated end signal) at or near the polyadenylation site. The normal end formation was abolished when the core signal was placed in the reverse orientation. A considerable fraction of pre-mRNA synthesized in vitro with SP6 RNA polymerase on the template of a DNA fragment containing these signals was cleaved and polyadenylated presumably at the in vitro 3' end during incubation in a cell-free system of yeast. By contrast pre-mRNA synthesized on the template with the core signal alone was processed but much less efficiently. No such processing was seen when the pre-mRNA either lacked the core signal or contained it in the reverse orientation.
引用
收藏
页码:3691 / 3697
页数:7
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