Monod C, Goldschmidt-Clermont M, Rochaix J D
Department of Molecular Biology, University of Geneva, Switzerland.
Mol Gen Genet. 1992 Feb;231(3):449-59. doi: 10.1007/BF00292715.
We have isolated and characterized a nuclear mutant, 222E, in Chlamydomonas reinhardtii, which is defective in photosystem II (PSII). Polypeptide P5, the product of psbB, is not produced in this mutant, leading to a destabilization of other PSII components. The mutant specifically fails to accumulate psbB transcripts and displays an altered transcription pattern downstream of psbB. Pulse-labelling experiments suggest that mRNA stability and/or processing are affected by the alteration of a nuclear gene product in this mutant. We show that the C. reinhardtii psbB gene is co-transcribed with a small open reading frame that is highly conserved in location and amino acid sequence in land plants. The 5' and 3' termini of the psbB transcript have been mapped to 35 bases upstream of the initiation codon and approximately 600 bases downstream of the stop codon. The 3' flanking region contains two potential stem-loops, of which the larger (with an estimated free energy of -46 kcal) is near the 3' terminus of the transcript.
我们已经在莱茵衣藻中分离并鉴定了一个核突变体222E,该突变体在光系统II(PSII)方面存在缺陷。多肽P5是psbB的产物,在这个突变体中不产生,导致其他PSII组件不稳定。该突变体特别不能积累psbB转录本,并在psbB下游显示出改变的转录模式。脉冲标记实验表明,该突变体中核基因产物的改变影响了mRNA的稳定性和/或加工过程。我们发现莱茵衣藻的psbB基因与一个小的开放阅读框共转录,该开放阅读框在陆生植物中的位置和氨基酸序列高度保守。psbB转录本的5'和3'末端已分别定位到起始密码子上游35个碱基处和终止密码子下游约600个碱基处。3'侧翼区域包含两个潜在的茎环结构,其中较大的一个(估计自由能为-46千卡)靠近转录本的3'末端。