Clarke A K, Gustafsson P, Lidholm J A
Department of Plant Physiology, University of Umeå, Sweden.
Plant Mol Biol. 1994 Nov;26(3):851-62. doi: 10.1007/BF00028853.
The clpP gene from the conifer Pinus contorta was identified and isolated from a chloroplast genomic library by heterologous hybridisation to the second exon of the chloroplast clpP gene in tobacco. DNA sequencing of two overlapping clones revealed an uninterrupted 615 bp open-reading frame with 41 to 65% similarity to the clpP genes in five other chloroplast genomes and Escherichia coli. The 615 bp sequence in P. contorta contained perfectly matched motifs for the serine and histidine active sites of the ClpP protease in E. coli. The location of the clpP gene was determined using a physical map of the P. contorta chloroplast genome, and was found to lie within a 10 kb region between the psbE/F and rpoB genes. Sequencing of the regions adjacent to the clpP gene revealed the first exon of the rps12 gene located 135 bp downstream. The genomic position of the first exon of the rps12 gene in relation to the clpP gene is conserved for all other chloroplast clpP genes identified so far. Northern blot analysis showed that the clpP gene in both P. contorta and P. sylvestris was present in several transcript of different length, ranging from 0.8 to 2.4 kb. The two longer transcripts in P. contorta also included the first exon of the rps12 gene. Mapping of the 5' end of the clpP transcripts by primer extension, however, revealed a single transcription initiation site 53 bp upstream of the first ATG codon. Analysis of total RNA isolated from the two pine species grown in darkness or moderate light conditions (250 mumol photons m-2 s-1) showed no significance difference in the level of expression of the clpP gene. The results suggest that the clpP gene in conifers is part of an operon which includes the first exon of the rps12 and the entire rpl20 gene, and is expressed in a light-independent manner as a polycistronic precursor which later undergoes post-transcriptional processing to give the mature monocistronic clpP mRNA.
通过与烟草叶绿体clpP基因的第二个外显子进行异源杂交,从叶绿体基因组文库中鉴定并分离出了来自针叶树扭叶松的clpP基因。对两个重叠克隆进行DNA测序,结果显示有一个615 bp的不间断开放阅读框,与其他五个叶绿体基因组以及大肠杆菌中的clpP基因具有41%至65%的相似性。扭叶松中的615 bp序列包含与大肠杆菌中ClpP蛋白酶的丝氨酸和组氨酸活性位点完全匹配的基序。利用扭叶松叶绿体基因组的物理图谱确定了clpP基因的位置,发现它位于psbE/F和rpoB基因之间的一个10 kb区域内。对clpP基因相邻区域进行测序,发现rps12基因的第一个外显子位于其下游135 bp处。到目前为止,已鉴定出的所有其他叶绿体clpP基因中,rps12基因第一个外显子相对于clpP基因的基因组位置都是保守的。Northern杂交分析表明,扭叶松和欧洲赤松中的clpP基因存在于几种不同长度的转录本中,长度范围为0.8至2.4 kb。扭叶松中两个较长的转录本还包含rps12基因的第一个外显子。然而,通过引物延伸对clpP转录本的5'端进行定位,结果显示在第一个ATG密码子上游53 bp处有一个单一的转录起始位点。对在黑暗或中等光照条件(250 μmol光子·m⁻²·s⁻¹)下生长的这两种松树分离得到的总RNA进行分析,结果表明clpP基因的表达水平没有显著差异。这些结果表明,针叶树中的clpP基因是一个操纵子的一部分,该操纵子包括rps12的第一个外显子和整个rpl20基因,并且以多顺反子前体形式进行不依赖光的表达,随后经过转录后加工产生成熟的单顺反子clpP mRNA。