Deletion of rpoB reveals a second distinct transcription system in plastids of higher plants

被引:288
作者
Allison, LA [1 ]
Simon, LD [1 ]
Maliga, P [1 ]
机构
[1] RUTGERS STATE UNIV,WAKSMAN INST,PISCATAWAY,NJ 08855
关键词
biolistic transformation; plastid promoter; plastid RNA polymerase; rpoB gene; tobacco;
D O I
10.1002/j.1460-2075.1996.tb00640.x
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
The plastid genome in higher plants encodes subunits of an Escherichia coli-like RNA polymerase which initiates transcription of plastid genes from sequences resembling E.coli sigma(70)-type promoters. By deleting the gene for the essential beta subunit of the tobacco E.coli-like RNA polymerase, we have established the existence of a second plastid transcription system which does not utilize E.coli-like promoters. In contrast to the E.coli-like RNA polymerase, the novel transcription machinery preferentially transcribes genetic system genes rather than photosynthetic genes. Although the mutant plants are photosynthetically defective, transcription by this polymerase is sufficient for plastid maintenance and plant development.
引用
收藏
页码:2802 / 2809
页数:8
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