Liere K, Link G
Arbeitsgruppe Pflanzliche Zellphysiologie und Molekularbiologie, Fakultät für Biologie, Ruhr-Universität Bochum, Germany.
Curr Genet. 1994 Nov-Dec;26(5-6):557-63. doi: 10.1007/BF00309950.
The mustard chloroplast gene trnG-UCC is split by a 717-bp group-II intron. Northern hybridization and RNase protection experiments suggest cotranscription with the upstream psbK-psbI operon, but not with the downstream trnR-UCU gene. The ends of most RNase-protected fragments between psbI and trnG correlate with the position of two potential stem-loop structures in this region, which could act as RNA processing elements. However, one RNA 5' end, approximately 75 bp upstream of the trnG 5' exon, does not so correlate and is preceded by prokaryotic-type '-10' and '-35' sequence elements. This suggests the possibility that a fraction of the trnG transcripts is initiated here. All precursor transcripts spanning the trnG region seem to have a common 3' end, which was located 117 bp downstream from the 3' exon, immediately after a stem-loop region. During seedling development, the major 0.8-0.9-kb trnG precursor transcripts show a transient maximum level at around 48 h after sowing, at a time when the mature tRNA begins to accumulate to constant levels. No significant differences in transcript patterns were observed either in the light or in darkness.
芥菜叶绿体基因trnG-UCC被一个717bp的II类内含子隔开。Northern杂交和RNase保护实验表明,它与上游的psbK-psbI操纵子共转录,但不与下游的trnR-UCU基因共转录。psbI和trnG之间大多数RNase保护片段的末端与该区域两个潜在的茎环结构位置相关,这两个结构可能作为RNA加工元件。然而,一个RNA 5'末端位于trnG 5'外显子上游约75bp处,并不符合这种情况,且其前面有原核生物类型的“-10”和“-35”序列元件。这表明trnG转录本的一部分可能在此处起始。所有跨越trnG区域的前体转录本似乎都有一个共同的3'末端,该末端位于3'外显子下游117bp处,紧接在一个茎环区域之后。在幼苗发育过程中,主要的0.8 - 0.9kb trnG前体转录本在播种后约48小时显示出短暂的最高水平,此时成熟tRNA开始积累至恒定水平。在光照或黑暗条件下,转录本模式均未观察到显著差异。