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HIGHER-ORDER STRUCTURE OF THE 5.8-S RIBOSOMAL-RNA SEQUENCE WITHIN THE YEAST 35-S PRECURSOR RIBOSOMAL-RNA SYNTHESIZED INVITRO
被引:15
|
作者
:
YEH, LCC
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Biochemistry The University, Texas Health Science Center at San Antonio
YEH, LCC
LEE, JC
论文数:
0
引用数:
0
h-index:
0
机构:
Department of Biochemistry The University, Texas Health Science Center at San Antonio
LEE, JC
机构
:
[1]
Department of Biochemistry The University, Texas Health Science Center at San Antonio
来源
:
JOURNAL OF MOLECULAR BIOLOGY
|
1991年
/ 217卷
/ 04期
关键词
:
D O I
:
10.1016/0022-2836(91)90523-9
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
:
Dimethylsulfate, 1-cyclohexyl-3-(2-morpholinoethyl)-carbodiimide metho-p-toluene-sulfonate, RNase T1 and RNase V1 have been used as structure-sensitive probes to examine the higher-order structure of the 5.8 S rRNA sequence within the yeast 35 S precursor ribosomal RNA molecule. Data produced have been used to evaluate several theoretical structure models for the 5.8 S rRNA sequence within the precursor rRNA. These models are generated by minimum free energy calculations. A model is proposed that accommodates 83% of the residues experimentally shown to be in either base-paired or single-stranded structure in the correct configuration. Several alternative suboptimal secondary structures have been evaluated. Moreover, the chemical reactivities of several residues within the 5.8 S rRNA sequence in the precursor rRNA molecule differ from those of the corresponding residues in the mature rRNA molecule. This finding provides experimental evidence to support the notion that the 5.8 S rRNA sequence within the precursor rRNA undergoes structural reorganization following rRNA processing. © 1991.
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页码:649 / 659
页数:11
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