Rodio Maria-Elena, Delgado Sonia, De Stradis Angelo, Gómez María-Dolores, Flores Ricardo, Di Serio Francesco
Dipartimento di Protezione delle Piante e Microbiologia Applicata, Università degli Studi and Istituto di Virologia Vegetale del Consiglio Nazionale delle Ricerche, Sezione di Bari, 70126 Bari, Italy.
Plant Cell. 2007 Nov;19(11):3610-26. doi: 10.1105/tpc.106.049775. Epub 2007 Nov 30.
Peach latent mosaic viroid (PLMVd) is a chloroplast-replicating RNA that propagates in its natural host, peach (Prunus persica), as a complex mixture of variants, some of which are endowed with specific structural and pathogenic properties. This is the case of variant PC-C40, with an insertion of 12 to 13 nucleotides that folds into a hairpin capped by a U-rich loop, which is responsible for an albino-variegated phenotype known as peach calico (PC). We have applied a combination of ultrastructural, biochemical, and molecular approaches to dissect the pathogenic effects of PC-C40. Albino sectors of leaves infected with variant PC-C40 presented palisade cells that did not completely differentiate into a columnar layer and altered plastids with irregular shape and size and with rudimentary thylakoids, resembling proplastids. Furthermore, impaired processing and accumulation of plastid rRNAs and, consequently, of the plastid translation machinery was observed in the albino sectors of leaves infected with variant PC-C40 but not in the adjacent green areas or in leaves infected by mosaic-inducing or latent variants (including PC-C40Delta, in which the 12- to 13-nucleotide insertion was deleted). Protein gel blot and RT-PCR analyses showed that the altered plastids support the import of nucleus-encoded proteins, including a chloroplast RNA polymerase, the transcripts of which were detected. RNA gel blot and in situ hybridizations revealed that PLMVd replicates in the albino leaf sectors and that it can invade the shoot apical meristem and induce alterations in proplastids, bypassing the RNA surveillance system that restricts the entry of a nucleus-replicating viroid and most RNA viruses. Therefore, a non-protein-coding RNA with a specific structural motif can interfere with an early step of the chloroplast developmental program, leading ultimately to an albino-variegated phenotype resembling that of certain variegated mutants in which plastid rRNA maturation is also impaired. Our results highlight the potential of viroids for further dissection of RNA trafficking and pathogenesis in plants.
桃潜隐花叶类病毒(PLMVd)是一种在叶绿体中复制的RNA,它在其天然宿主桃树(Prunus persica)中以多种变体的复杂混合物形式传播,其中一些变体具有特定的结构和致病特性。变体PC-C40就是这样,它插入了12至13个核苷酸,折叠成一个由富含U的环封端的发夹结构,这导致了一种称为桃杂色病(PC)的白化斑驳表型。我们应用了超微结构、生化和分子方法相结合的手段来剖析PC-C40的致病作用。感染变体PC-C40的叶片白化区域呈现出栅栏细胞,这些细胞没有完全分化成柱状层,并且质体发生改变,形状和大小不规则,类囊体发育不全,类似于原质体。此外,在感染变体PC-C40的叶片白化区域中观察到质体rRNA的加工和积累受损,进而质体翻译机制也受到影响,但在相邻的绿色区域或感染花叶诱导型或潜伏型变体(包括PC-C40Delta,其中12至13个核苷酸的插入被删除)的叶片中未观察到这种情况。蛋白质凝胶印迹和RT-PCR分析表明,发生改变的质体支持核编码蛋白的导入,包括一种叶绿体RNA聚合酶,并且检测到了其转录本。RNA凝胶印迹和原位杂交显示,PLMVd在白化叶区域中复制,并且它可以侵入茎尖分生组织并诱导原质体发生改变,绕过了限制核复制类病毒和大多数RNA病毒进入的RNA监测系统。因此,一种具有特定结构基序的非蛋白质编码RNA可以干扰叶绿体发育程序的早期步骤,最终导致类似于某些斑驳突变体的白化斑驳表型,在这些突变体中质体rRNA的成熟也受到损害。我们的结果突出了类病毒在进一步剖析植物中RNA运输和发病机制方面的潜力。