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酵母杀伤病毒M1双链RNA的内部聚腺苷酸序列长度可变。

The internal polyadenylate tract of yeast killer virus M1 double-stranded RNA is variable in length.

作者信息

Hannig E M, Williams T L, Leibowitz M J

出版信息

Virology. 1986 Jul 15;152(1):149-58. doi: 10.1016/0042-6822(86)90380-6.

DOI:10.1016/0042-6822(86)90380-6
PMID:3521070
Abstract

The 1.8-kbp M1 double-stranded (ds) RNA from type 1 killer strains of Saccharomyces cerevisiae contains an internal 200-bp adenine- and uracil-rich region. We have previously demonstrated that this region consists primarily of adenine residues on the plus strand of M1 dsRNA and on the full-length, in vitro synthesized (+) transcript (denoted m) of M1 dsRNA, neither of which contains 3'-terminal polyadenylate. We now show that there is variability in the length of the polyadenylate tracts of m transcripts synthesized in vitro by virions purified from either of the K1 diploid killer strains A364A X S7 or A364A X 1384. This variability reflects size differences seen in the corresponding M1 dsRNA genomes which, along with other data presented, localizes the variability in the length of M1 dsRNA to the adenine- and uracil-rich region.

摘要

来自酿酒酵母1型杀伤菌株的1.8千碱基对的M1双链(ds)RNA包含一个内部200碱基对的富含腺嘌呤和尿嘧啶的区域。我们之前已经证明,该区域主要由M1双链RNA正链上的腺嘌呤残基以及M1双链RNA的全长体外合成(+)转录本(记为m)组成,这两者均不包含3'-末端聚腺苷酸。我们现在表明,从K1二倍体杀伤菌株A364A×S7或A364A×1384中纯化的病毒体在体外合成的m转录本的聚腺苷酸尾长度存在变异性。这种变异性反映了在相应的M1双链RNA基因组中观察到的大小差异,结合其他所呈现的数据,将M1双链RNA长度的变异性定位到富含腺嘌呤和尿嘧啶的区域。

相似文献

1
The internal polyadenylate tract of yeast killer virus M1 double-stranded RNA is variable in length.酵母杀伤病毒M1双链RNA的内部聚腺苷酸序列长度可变。
Virology. 1986 Jul 15;152(1):149-58. doi: 10.1016/0042-6822(86)90380-6.
2
Genome structure and expression of a defective interfering mutant of the killer virus of yeast.酵母杀伤病毒缺陷干扰突变体的基因组结构与表达
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Saccharomyces cerevisiae killer virus transcripts contain template-coded polyadenylate tracts.酿酒酵母杀伤病毒转录本含有模板编码的聚腺苷酸序列。
Mol Cell Biol. 1984 Jan;4(1):101-9. doi: 10.1128/mcb.4.1.101-109.1984.
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Yeast killer dsRNA plasmids are transcribed in vivo to produce full and partial-length plus-stranded RNAs.酵母杀手双链RNA质粒在体内转录以产生全长和部分长度的正链RNA。
Nucleic Acids Res. 1983 Feb 25;11(4):1077-97. doi: 10.1093/nar/11.4.1077.
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Sequence of the M1-2 region of killer virus double-stranded RNA.杀伤病毒双链RNA的M1-2区域序列。
Basic Life Sci. 1986;40:203-13. doi: 10.1007/978-1-4684-5251-8_16.
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Cloning and expression of a cDNA copy of the viral K28 killer toxin gene in yeast.病毒K28杀伤毒素基因cDNA拷贝在酵母中的克隆与表达。
Mol Gen Genet. 1995 Jan 20;246(2):236-46. doi: 10.1007/BF00294687.
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Cloning, sequencing and expression of a full-length cDNA copy of the M1 double-stranded RNA virus from the yeast, Saccharomyces cerevisiae.来自酿酒酵母的M1双链RNA病毒全长cDNA拷贝的克隆、测序及表达
Yeast. 1997 Jul;13(9):829-36. doi: 10.1002/(SICI)1097-0061(199707)13:9<829::AID-YEA144>3.0.CO;2-R.
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T double-stranded RNA (dsRNA) sequence reveals that T and W dsRNAs form a new RNA family in Saccharomyces cerevisiae. Identification of 23 S RNA as the single-stranded form of T dsRNA.T双链RNA(dsRNA)序列表明,T和W dsRNA在酿酒酵母中形成了一个新的RNA家族。鉴定出23S RNA为T dsRNA的单链形式。
J Biol Chem. 1992 May 25;267(15):10874-81.
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Synthesis of a double-stranded cDNA transcript of the killer toxin-coding region of the yeast M1 double-stranded RNA.酵母M1双链RNA杀伤毒素编码区双链cDNA转录本的合成。
Biochem Biophys Res Commun. 1983 Jul 29;114(2):518-25. doi: 10.1016/0006-291x(83)90811-2.
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A deletion mutant of L-A double-stranded RNA replicates like M1 double-stranded RNA.L-A双链RNA的缺失突变体像M1双链RNA一样进行复制。
J Virol. 1988 Apr;62(4):1278-85. doi: 10.1128/JVI.62.4.1278-1285.1988.

引用本文的文献

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New developments in fungal virology.真菌病毒学的新进展。
Adv Virus Res. 1994;43:303-88. doi: 10.1016/s0065-3527(08)60052-4.
2
His-154 is involved in the linkage of the Saccharomyces cerevisiae L-A double-stranded RNA virus Gag protein to the cap structure of mRNAs and is essential for M1 satellite virus expression.组氨酸-154参与酿酒酵母L-A双链RNA病毒Gag蛋白与mRNA帽结构的连接,对M1卫星病毒的表达至关重要。
Mol Cell Biol. 1994 Apr;14(4):2664-74. doi: 10.1128/mcb.14.4.2664-2674.1994.
3
Terminal structure of hypovirulence-associated dsRNAs in the chestnut blight fungus Endothia parasitica.
栗疫病菌寄生内座壳中低毒力相关双链RNA的末端结构
Nucleic Acids Res. 1986 Dec 22;14(24):9877-96. doi: 10.1093/nar/14.24.9877.