Shepherd H S, Boynton J E, Gillham N W
Proc Natl Acad Sci U S A. 1979 Mar;76(3):1353-7. doi: 10.1073/pnas.76.3.1353.
Chloroplast components known to be coded by chloroplast DNA include chloroplast rRNAs, tRNAs, and the large subunit of ribulose-bisphosphate carboxylase. Because these components comprise less than 3% of the estimated coding capacity of the chloroplast genome, most chloroplast gene functions have yet to be identified. One approach to this problem is the isolation and characterization of mutations in the chloroplast genome affecting specific photosynthetic functions. Recently we have found that such mutations can be preferentially recovered by using arsenate selection on cells previously grown in 5-fluorodeoxyuridine. Sixteen mutants thus isolated have been localized into nine chloroplast loci, based on their ability to recombine and produce photosynthetically competent progeny. Mutants at two loci show the characteristic syndrome of photosynthetic defects that results from a deficiency in chloroplast protein synthesis. These have been found to lack chloroplast ribosome monomers. Mutants at three loci are missing chlorophyll-protein complex I in their thylakoid membranes. Mutants at three other loci are deficient in membrane polypeptides known to be associated with the chloroplast coupling factor.
已知由叶绿体DNA编码的叶绿体成分包括叶绿体rRNA、tRNA以及核酮糖-1,5-二磷酸羧化酶的大亚基。由于这些成分占叶绿体基因组估计编码能力的不到3%,大多数叶绿体基因功能尚未被确定。解决这个问题的一种方法是分离和鉴定影响特定光合功能的叶绿体基因组中的突变。最近我们发现,通过对先前在5-氟脱氧尿苷中生长的细胞进行砷酸盐选择,可以优先恢复此类突变。基于它们重组并产生光合能力后代的能力,由此分离出的16个突变体已被定位到9个叶绿体基因座。两个基因座的突变体表现出由于叶绿体蛋白质合成缺陷导致的光合缺陷特征综合征。已发现这些突变体缺乏叶绿体核糖体单体。三个基因座的突变体在其类囊体膜中缺失叶绿素-蛋白质复合体I。其他三个基因座的突变体缺乏已知与叶绿体偶联因子相关的膜多肽。