Pouteau S, Spielmann A, Meyer C, Grandbastien M A, Caboche M
Laboratoire de Biologie Cellulaire, INRA, Versailles, France.
Mol Gen Genet. 1991 Aug;228(1-2):233-9. doi: 10.1007/BF00282471.
The effects of Tnt1 retrotransposon insertion on nitrate reductase (NR) gene transcription have been analyzed in three NR-deficient insertional, mutants of Nicotiana tabacum. In the three mutants, named h9-Nia4, h9-Nia5 and h9-Nia6, Tnt1 was inserted into exon 3, exon 2 and exon 1 of the nia2 NR alloallelle, respectively. The mutants h9-Nia4 and h9-Nia6, which contained Tnt1 insertions that were oriented opposite to the direction of nia2 gene transcription, expressed chimaeric nia2-Tnt1 RNAs, respectively 12 kb and 10 kb long. The size observed in h9-Nia6 was close to the expected size for a full-length hybrid transcript starting and ending under the control of nia2 signals (about 9 kb). The larger transcript found in h9-Nia4 was shown to be due to a failure to splice the nia2 intron 2. The mutant h9-Nia5, which contained a Tnt1 insertion oriented in parallel with the direction of nia2 transcription expressed two truncated nia2-Tnt1 RNAs, 2 kb and 6.7 kb long. These transcripts arose from termination in the long terminal repeats (LTRs) of Tnt1. Since no full-length hybrid RNA was detected, we suggest that Tnt1 carries efficient termination signals, which are more efficiently recognized in the 3' LTR than in the 5' LTR.
在烟草的三个硝酸盐还原酶(NR)缺陷型插入突变体中,分析了Tnt1逆转座子插入对NR基因转录的影响。在这三个分别命名为h9-Nia4、h9-Nia5和h9-Nia6的突变体中,Tnt1分别插入到nia2 NR等位基因的外显子3、外显子2和外显子1中。h9-Nia4和h9-Nia6这两个突变体,其Tnt1插入方向与nia2基因转录方向相反,分别表达了长度为12 kb和10 kb的嵌合nia2-Tnt1 RNA。在h9-Nia6中观察到的大小接近在nia2信号控制下起始和终止的全长杂交转录本的预期大小(约9 kb)。在h9-Nia4中发现的较大转录本被证明是由于未能剪接nia2内含子2。h9-Nia5突变体含有一个与nia2转录方向平行的Tnt1插入,表达了两种截短的nia2-Tnt1 RNA,长度分别为2 kb和6.7 kb。这些转录本源于Tnt1长末端重复序列(LTR)中的终止。由于未检测到全长杂交RNA,我们认为Tnt1携带有效的终止信号,这些信号在3' LTR中比在5' LTR中更有效地被识别。