Ruiz-Sola M Águila, Barja M Victoria, Manzano David, Llorente Briardo, Schipper Bert, Beekwilder Jules, Rodriguez-Concepcion Manuel
Program of Plant Metabolism and Metabolic Engineering, Centre for Research in Agricultural Genomics (CRAG) CSIC-IRTA-UAB-UB, Campus UAB Bellaterra, 08193 Barcelona, Spain (M.A.R.-S., M.V.B., D.M., B.L., M.R.-C.); and.
Plant Research International, 6700 AA Wageningen, The Netherlands (B.S., J.B.).
Plant Physiol. 2016 Nov;172(3):1393-1402. doi: 10.1104/pp.16.01392. Epub 2016 Oct 5.
A wide diversity of isoprenoids is produced in different plant compartments. Most groups of isoprenoids synthesized in plastids, and some produced elsewhere in the plant cell derive from geranylgeranyl diphosphate (GGPP) synthesized by GGPP synthase (GGPPS) enzymes. In Arabidopsis (Arabidopsis thaliana), five genes appear to encode GGPPS isoforms localized in plastids (two), the endoplasmic reticulum (two), and mitochondria (one). However, the loss of function of the plastid-targeted GGPPS11 isoform (referred to as G11) is sufficient to cause lethality. Here, we show that the absence of a strong transcription initiation site in the G11 gene results in the production of transcripts of different lengths. The longer transcripts encode an isoform with a functional plastid import sequence that produces GGPP for the major groups of photosynthesis-related plastidial isoprenoids. However, shorter transcripts are also produced that lack the first translation initiation codon and rely on a second in-frame ATG codon to produce an enzymatically active isoform lacking this N-terminal domain. This short enzyme localizes in the cytosol and is essential for embryo development. Our results confirm that the production of differentially targeted enzyme isoforms from the same gene is a central mechanism to control the biosynthesis of isoprenoid precursors in different plant cell compartments.
不同的类异戊二烯在植物的不同区室中产生。大多数在质体中合成的类异戊二烯基团,以及在植物细胞其他部位产生的一些类异戊二烯,都源自由牻牛儿基牻牛儿基二磷酸合酶(GGPPS)合成的牻牛儿基牻牛儿基二磷酸(GGPP)。在拟南芥中,五个基因似乎编码定位于质体(两个)、内质网(两个)和线粒体(一个)的GGPPS同工型。然而,质体靶向的GGPPS11同工型(称为G11)功能丧失足以导致致死性。在这里,我们表明G11基因中缺乏强转录起始位点会导致产生不同长度的转录本。较长的转录本编码一种具有功能性质体导入序列的同工型,该序列为主要的光合作用相关质体类异戊二烯基团产生GGPP。然而,也会产生较短的转录本,这些转录本缺乏第一个翻译起始密码子,并依赖第二个框内ATG密码子来产生一种缺乏该N端结构域的酶活性同工型。这种短酶定位于细胞质中,对胚胎发育至关重要。我们的结果证实,从同一基因产生差异靶向的酶同工型是控制不同植物细胞区室中类异戊二烯前体生物合成的核心机制。