HIGH-LEVEL RIBOSOMAL FRAMESHIFTING DIRECTS THE SYNTHESIS OF IS150 GENE-PRODUCTS

被引:85
作者
VOGELE, K
SCHWARTZ, E
WELZ, C
SCHILTZ, E
RAK, B
机构
[1] UNIV FREIBURG,INST BIOL 3,SCHANZLESTR 1,W-7800 FREIBURG,GERMANY
[2] UNIV FREIBURG,INST ORGAN CHEM & BIOCHEM,W-7800 FREIBURG,GERMANY
关键词
D O I
10.1093/nar/19.16.4377
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
IS150 contains two tandem, out-of-phase, overlapping genes, ins150A and ins150B, which are controlled by the same promoter. These genes encode proteins of 19 and 31 kD, respectively. A third protein of 49kD is a transframe gene product consisting of domains encoded by both genes. Specific -1 ribosomal frameshifting is responsible for the synthesis of the large protein. Expression of ins150B also involves frameshifting. The IS150 frameshifting signals operate with a remarkably high efficiency, causing about one third of the ribosomes to switch frame. All of the signals required for this process are encoded in a 83-bp segment of the element. The heptanucleotide A AAA AAG and a potential stem-loop-forming sequence mark the frameshifting site. Similar sequence elements are found in -1 frameshifting regions of bacterial and retroviral genes. A mutation within the stem-loop sequence reduces the rate of frameshifting by about 80%. Artificial transposons carrying this mutation transpose at a normal frequency, but form cointegrates at a almost-equal-to 100-fold reduced rate.
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页码:4377 / 4385
页数:9
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