Freyer R, Neckermann K, Maier R M, Kössel H
Institut für Biologie III, Universität Freiburg, Germany.
Curr Genet. 1995 May;27(6):580-6. doi: 10.1007/BF00314451.
The gene cluster rps12/rps7/psi ndhB of the plastome from the holoparasitic plant Cuscuta europaea has been analysed at the nucleotide level. A comparison with the homologous region of the plastome from the closely related parasite Cuscuta reflexa reveals a complete loss of the cis-spliced intron of the rps12 gene in addition to a drastic size reduction of the ndhB pseudogene. It is demonstrated by RT-PCR analysis that the entire gene cluster is transcribed in the form of a multicistronic transcript which also includes the sequences encoded by the ndhB pseudogene. A cDNA containing the correctly transpliced exon 1 of the rps12 transcript can also be amplified. This shows that trans-splicing of the rps12 transcript persists in the plastids of the holoparasite despite the loss of the cis-spliced intron and the loss of many other gene functions. The rps12 and rps7 genes, therefore, still appear to code for functional ribosomal proteins CS12 and CS7, respectively. The conservation of apparently intact ribosomal-protein genes from which correctly processed transcripts are produced is taken as evidence that the translational apparatus of the plastids is still functional and necessary for the expression of the genes remaining in the reduced plastome of a parasitic plant.
已在核苷酸水平上分析了全寄生植物欧洲菟丝子质体基因组的基因簇rps12/rps7/ψndhB。与近缘寄生植物反折菟丝子质体基因组的同源区域进行比较发现,rps12基因的顺式剪接内含子完全缺失,此外ndhB假基因的大小也大幅减小。RT-PCR分析表明,整个基因簇以多顺反子转录本的形式转录,该转录本还包括ndhB假基因编码的序列。还可以扩增出包含rps12转录本正确反式剪接外显子1的cDNA。这表明,尽管顺式剪接内含子缺失且许多其他基因功能丧失,但rps12转录本的反式剪接在全寄生植物的质体中仍然存在。因此,rps12和rps7基因似乎仍分别编码功能性核糖体蛋白CS12和CS7。产生正确加工转录本的明显完整核糖体蛋白基因的保守性被视为质体翻译装置仍然具有功能且对于寄生植物简化质体基因组中剩余基因的表达必不可少的证据。