NONENZYMATIC CLEAVAGE AND LIGATION OF RNAS COMPLEMENTARY TO A PLANT-VIRUS SATELLITE RNA
NONENZYMATIC CLEAVAGE AND LIGATION OF RNAS COMPLEMENTARY TO A PLANT-VIRUS SATELLITE RNA
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DOI:
10.1038/323349a0
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发表时间:
1986-09-25
期刊:
影响因子:
64.8
通讯作者:
BRUENING, G
中科院分区:
文献类型:
--
作者:
BUZAYAN, JM;GERLACH, WL;BRUENING, G
Small satellite RNAs1–5of plant viruses depend on the presence of a supporting RNA virus for their propagationin vivo. Replication of the 359–nucleotide-long6satellite RNA of tobacco ringspot virus (STobRV RNA) is detected only in tissue infected with tobacco ringspot virus (TobRV). STobRV RNA becomes encapsidated in TobRV coat protein and acts as a parasite of TobRV, reducing its accumulation and the severity of symptoms that it induces. Here we report the transcriptionin vitroof a circularly permuted, complementary DNA clone of STobRV RNA oriented so as to produce RNA that is complementary to the encapsidated, (+) polarity STobRV RNA. Like STobRV (+)RNA7, this dimeric, circularly permuted STobRV (−)RNA cleaves autolytically. Cleavage is at two identical sites generating monomeric-length RNA and two terminal fragments. The new termini are 5′-hydroxyl and 2′:3′-cyclic phosphodiester groups. The RNAs ligate spontaneously to give linear and, from the monomers, circular molecules. Replication of STobRV RNA may require these autoly-sis and ligation reactions, which, at leastin vitro, occur without enzyme catalysis.