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PROCESSING AND EXPRESSION OF EARLY SV40 MESSENGER-RNA - ROLE FOR RNA CONFORMATION IN SPLICING
被引:111
作者
:
KHOURY, G
论文数:
0
引用数:
0
h-index:
0
机构:
Laboratory of Molecular Virology National Cancer Institute Bethesda
KHOURY, G
GRUSS, P
论文数:
0
引用数:
0
h-index:
0
机构:
Laboratory of Molecular Virology National Cancer Institute Bethesda
GRUSS, P
DHAR, R
论文数:
0
引用数:
0
h-index:
0
机构:
Laboratory of Molecular Virology National Cancer Institute Bethesda
DHAR, R
LAI, CJ
论文数:
0
引用数:
0
h-index:
0
机构:
Laboratory of Molecular Virology National Cancer Institute Bethesda
LAI, CJ
机构
:
[1]
Laboratory of Molecular Virology National Cancer Institute Bethesda
来源
:
CELL
|
1979年
/ 18卷
/ 01期
关键词
:
D O I
:
10.1016/0092-8674(79)90356-8
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
:
Early deletion mutants of SV40 were studied in an attempt to determine the nucleotide sequences which affect the processing and stability of the two major early SV40 mRNAs. The early SV40 mutants with deletions between 0.53 and 0.60 map units (54/59 mutants) are viable in tissue culture infections. While all of these early viable mutants contain deletions in the intervening sequences for the large T antigen, results from transcriptional mapping showed that none of them appears to affect the sites or frequency of splicing for large T-mRNA. The 54/59 mutants in which the deletion removes the proximal small t splice junction make no discrete stable cytoplasmic small t-mRNA. Those 54/59 mutants with deletions that do not include the splice junction synthesize discrete and predictably shortened small t-mRNAs. The size and location of the specific deletions, however, appear to affect significantly the abundance of the altered transcripts; this probably reflects the frequency with which the splice is made. These findings suggest that both the primary sequence near the splice junctions and the secondary or tertiary RNA structure influence the location and frequency with which a particular splicing event occurs. In addition, SDS-polyacrylamide gel analysis of the early SV40 polypeptides synthesized by the 54/59 mutants has suggested a direct relationship between the abundance of an mRNA and the amount of the corresponding polypeptide. These results suggest that the synthesis of the early SV40 proteins is regulated primarily by the synthesis and processing of a particular mRNA, rather than by translational or posttranslational controls. © 1979.
引用
收藏
页码:85 / 92
页数:8
相关论文
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[21]
COMMON METHIONINE-TRYPTIC PEPTIDES NEAR AMINO-TERMINAL END OF PRIMATE PAPOVAVIRUS TUMOR ANTIGENS
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SIMMONS, DT
MARTIN, MA
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MARTIN, MA
[J].
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA,
1978,
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: 1131
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1135
[22]
MUTANTS OF SV40 WITH AN ALTERED SMALL T-PROTEIN ARE REDUCED IN THEIR ABILITY TO TRANSFORM CELLS
SLEIGH, MJ
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SLEIGH, MJ
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HANICH, R
SAMBROOK, JF
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0
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0
h-index:
0
SAMBROOK, JF
[J].
CELL,
1978,
14
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88
[23]
MODIFICATION OF SIMIAN VIRUS-40 PROTEIN-A
TEGTMEYER, P
论文数:
0
引用数:
0
h-index:
0
机构:
SUNY STONY BROOK,DEPT MICROBIOL,STONY BROOK,NY 11790
SUNY STONY BROOK,DEPT MICROBIOL,STONY BROOK,NY 11790
TEGTMEYER, P
RUNDELL, K
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SUNY STONY BROOK,DEPT MICROBIOL,STONY BROOK,NY 11790
SUNY STONY BROOK,DEPT MICROBIOL,STONY BROOK,NY 11790
COLLINS, JK
[J].
JOURNAL OF VIROLOGY,
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[24]
THIMMAPPAYA B, J VIROL
[25]
MUTATIONAL ALTERATIONS WITHIN THE SIMIAN-VIRUS 40 LEADER SEGMENT GENERATE ALTERED 16S-MESSENGER RNA AND 19S-MESSENGER RNA
VILLARREAL, LP
论文数:
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引用数:
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h-index:
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机构:
STANFORD UNIV,SCH MED,DEPT BIOCHEM,STANFORD,CA 94305
STANFORD UNIV,SCH MED,DEPT BIOCHEM,STANFORD,CA 94305
VILLARREAL, LP
WHITE, RT
论文数:
0
引用数:
0
h-index:
0
机构:
STANFORD UNIV,SCH MED,DEPT BIOCHEM,STANFORD,CA 94305
STANFORD UNIV,SCH MED,DEPT BIOCHEM,STANFORD,CA 94305
WHITE, RT
BERG, P
论文数:
0
引用数:
0
h-index:
0
机构:
STANFORD UNIV,SCH MED,DEPT BIOCHEM,STANFORD,CA 94305
STANFORD UNIV,SCH MED,DEPT BIOCHEM,STANFORD,CA 94305
BERG, P
[J].
JOURNAL OF VIROLOGY,
1979,
29
(01)
: 209
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219
←
1
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3
→
共 25 条
[21]
COMMON METHIONINE-TRYPTIC PEPTIDES NEAR AMINO-TERMINAL END OF PRIMATE PAPOVAVIRUS TUMOR ANTIGENS
SIMMONS, DT
论文数:
0
引用数:
0
h-index:
0
SIMMONS, DT
MARTIN, MA
论文数:
0
引用数:
0
h-index:
0
MARTIN, MA
[J].
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA,
1978,
75
(03)
: 1131
-
1135
[22]
MUTANTS OF SV40 WITH AN ALTERED SMALL T-PROTEIN ARE REDUCED IN THEIR ABILITY TO TRANSFORM CELLS
SLEIGH, MJ
论文数:
0
引用数:
0
h-index:
0
SLEIGH, MJ
TOPP, WC
论文数:
0
引用数:
0
h-index:
0
TOPP, WC
HANICH, R
论文数:
0
引用数:
0
h-index:
0
HANICH, R
SAMBROOK, JF
论文数:
0
引用数:
0
h-index:
0
SAMBROOK, JF
[J].
CELL,
1978,
14
(01)
: 79
-
88
[23]
MODIFICATION OF SIMIAN VIRUS-40 PROTEIN-A
TEGTMEYER, P
论文数:
0
引用数:
0
h-index:
0
机构:
SUNY STONY BROOK,DEPT MICROBIOL,STONY BROOK,NY 11790
SUNY STONY BROOK,DEPT MICROBIOL,STONY BROOK,NY 11790
TEGTMEYER, P
RUNDELL, K
论文数:
0
引用数:
0
h-index:
0
机构:
SUNY STONY BROOK,DEPT MICROBIOL,STONY BROOK,NY 11790
SUNY STONY BROOK,DEPT MICROBIOL,STONY BROOK,NY 11790
RUNDELL, K
COLLINS, JK
论文数:
0
引用数:
0
h-index:
0
机构:
SUNY STONY BROOK,DEPT MICROBIOL,STONY BROOK,NY 11790
SUNY STONY BROOK,DEPT MICROBIOL,STONY BROOK,NY 11790
COLLINS, JK
[J].
JOURNAL OF VIROLOGY,
1977,
21
(02)
: 647
-
657
[24]
THIMMAPPAYA B, J VIROL
[25]
MUTATIONAL ALTERATIONS WITHIN THE SIMIAN-VIRUS 40 LEADER SEGMENT GENERATE ALTERED 16S-MESSENGER RNA AND 19S-MESSENGER RNA
VILLARREAL, LP
论文数:
0
引用数:
0
h-index:
0
机构:
STANFORD UNIV,SCH MED,DEPT BIOCHEM,STANFORD,CA 94305
STANFORD UNIV,SCH MED,DEPT BIOCHEM,STANFORD,CA 94305
VILLARREAL, LP
WHITE, RT
论文数:
0
引用数:
0
h-index:
0
机构:
STANFORD UNIV,SCH MED,DEPT BIOCHEM,STANFORD,CA 94305
STANFORD UNIV,SCH MED,DEPT BIOCHEM,STANFORD,CA 94305
WHITE, RT
BERG, P
论文数:
0
引用数:
0
h-index:
0
机构:
STANFORD UNIV,SCH MED,DEPT BIOCHEM,STANFORD,CA 94305
STANFORD UNIV,SCH MED,DEPT BIOCHEM,STANFORD,CA 94305
BERG, P
[J].
JOURNAL OF VIROLOGY,
1979,
29
(01)
: 209
-
219
←
1
2
3
→