Johnson C H, Schmidt G W
Department of Botany, University of Georgia, Athens 30602.
Plant Mol Biol. 1993 Jul;22(4):645-58. doi: 10.1007/BF00047405.
We have sequenced and characterized the complete psbB gene cluster of Chlamydomonas reinhardtii chloroplast DNA. Although the petB and petD genes are located elsewhere, the sequential order of psbB, ORF31, psbN and psbH is identical to that of the psbB operon in higher plants. Also, intergenic non-coding regions are much larger in the Chlamydomonas gene cluster. Northern blot analyses indicate the formation of dicistronic transcripts of psbB and ORF31 and monocistronic transcripts of psbN and psbH. It is unclear whether a psbB operon is transcribed to yield a large polycistronic precursor but northern blot analysis with total RNA from cells grown at 15 degrees C does not detect an increased complexity of the transcripts, as has been found in studies of the psbB operon of higher plants. From primer extension and nuclease protection assays, it is apparent that 5' and 3' processing of the primary psbH transcript results in the accumulation of a heterogenous population of mRNAs. Northern blot analyses reveal transcription of Chlamydomonas psbN and show that its mRNA is much larger than that identified in liverwort and pea. The sequence identities of the PSII-H and PSII-N polypeptides as compared to their vascular plant counterparts is 50 to 62%. While the amino acid sequences of PSII-H and PSII-N proteins are significantly conserved, the mass of PSII-H from Chlamydomonas is significantly larger.
我们对莱茵衣藻叶绿体DNA的完整psbB基因簇进行了测序和特征分析。尽管petB和petD基因位于其他位置,但psbB、ORF31、psbN和psbH的顺序与高等植物中psbB操纵子的顺序相同。此外,衣藻基因簇中的基因间非编码区要大得多。Northern印迹分析表明形成了psbB和ORF31的双顺反子转录本以及psbN和psbH的单顺反子转录本。目前尚不清楚psbB操纵子是否转录产生一个大的多顺反子前体,但用15摄氏度下生长的细胞的总RNA进行的Northern印迹分析未检测到转录本复杂性增加,这与高等植物psbB操纵子的研究结果一致。通过引物延伸和核酸酶保护试验可以明显看出,初级psbH转录本的5'和3'加工导致了异质mRNA群体的积累。Northern印迹分析揭示了衣藻psbN的转录,并表明其mRNA比在叶苔和豌豆中鉴定的mRNA大得多。与维管植物对应物相比,PSII-H和PSII-N多肽的序列同一性为50%至62%。虽然PSII-H和PSII-N蛋白的氨基酸序列显著保守,但衣藻的PSII-H质量明显更大。