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噬菌体MB78主要衣壳蛋白基因上游调控区域的多个拷贝会抑制噬菌体形态发生。

Multiple copies of the upstream regulatory region of the major capsid protein gene of bacteriophage MB78 inhibit phage morphogenesis.

作者信息

Sharma R, Ghosh A N, Datta P, Gupta L, Chakravorty M

机构信息

Molecular Biology Unit, Institute of Medical Sciences, Banaras Hindu University, Varanasi, UP, India.

出版信息

Virus Genes. 2001 Mar;22(2):151-8. doi: 10.1023/a:1008169111799.

Abstract

The 2.311 kb EcoRI F fragment of bacteriophage MB78 has been cloned in multicopy vectors pUC19 and pCR90. Salmonella typhimurium strains carrying such plasmids cannot support development of phage MB78 while other Salmonella phages like P22 and 9NA grow normally. Most of the phage MB78 induced functions are normal in such transformed hosts but proper maturation of the phage particles does not take place. Deletion of 138 bp from the 3' end of the cloned fragment reverses the inhibitory effect. Analysis of nucleotide and the deduced amino acid sequence of a 1.2 kb HindIII-SalI fragment of the phage genome which overlaps the 138 bp confirms that this part contains the upstream regulatory region of the major structural protein gene. It seems that in presence of multiple copies of the upstream regulatory region (which includes a number of promoter like sequence) of the coat protein gene, the maturase gene is down regulated and this is effective only in cis, a situation quite similar to that of Qbeta RNA phages.

摘要

噬菌体MB78的2.311 kb EcoRI F片段已被克隆到多拷贝载体pUC19和pCR90中。携带此类质粒的鼠伤寒沙门氏菌菌株不能支持噬菌体MB78的生长,而其他沙门氏菌噬菌体如P22和9NA则能正常生长。在这种转化宿主中,大多数噬菌体MB78诱导的功能是正常的,但噬菌体颗粒不能正常成熟。从克隆片段的3'端缺失138 bp可逆转抑制作用。对与138 bp重叠的噬菌体基因组1.2 kb HindIII-SalI片段的核苷酸和推导氨基酸序列分析证实,该部分包含主要结构蛋白基因的上游调控区。似乎在衣壳蛋白基因上游调控区(包括许多类似启动子的序列)多拷贝存在的情况下,成熟酶基因被下调,且这种情况仅在顺式作用中有效,这与Qβ RNA噬菌体的情况非常相似。

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