Howles Paul A, Birch Rosemary J, Collings David A, Gebbie Leigh K, Hurley Ursula A, Hocart Charles H, Arioli Tony, Williamson Richard E
Plant Cell Biology Group, Research School of Biological Sciences, Australian National University, Canberra, ACT 2601, Australia.
Plant J. 2006 Nov;48(4):606-18. doi: 10.1111/j.1365-313X.2006.02902.x. Epub 2006 Oct 19.
The Arabidopsis radial swelling mutant rsw10 showed ballooning of root trichoblasts, a lower than wild-type level of cellulose and altered levels of some monosaccharides in non-cellulosic polysaccharides. Map-based cloning showed that the mutated gene (At1g71100) encodes a ribose 5-phosphate isomerase (RPI) and that the rsw10 mutation replaces a conserved glutamic acid residue with lysine. Although RPI is intimately involved with many biochemical pathways, media supplementation experiments suggest that the visible phenotype results from a defect in the production of pyrimidine-based sugar-nucleotide compounds, most likely uridine 5'-diphosphate-glucose, the presumed substrate of cellulose synthase. Two of three RPI sequences in the nuclear genome are cytoplasmic, while the third has a putative chloroplast transit sequence. The sequence encoding both cytoplasmic enzymes could complement the mutation when expressed behind the CaMV 35S promoter, while fusion of the RSW10 promoter region to the GUS reporter gene established that the gene is expressed in many aerial tissues as well as the roots. The prominence of the rsw10 phenotype in roots probably reflects RSW10 being the only cytosolic RPI in this tissue and the gene encoding the plastid RPI being relatively weakly expressed. We could not, however, detect a decrease in total RPI activity in root extracts. The rsw10 phenotype is prominent near the root tip where cells undergo division, endoreduplication and cell expansion and so are susceptible to a restriction in de novo pyrimidine production. The two cytosolic RPIs probably arose in an ancient duplication event, their present expression patterns representing subfunctionalization of the expression of the original ancestral gene.
拟南芥径向肿胀突变体rsw10表现出根毛细胞的气球样膨大、纤维素水平低于野生型以及非纤维素多糖中一些单糖水平的改变。图位克隆表明,突变基因(At1g71100)编码一种磷酸核糖异构酶(RPI),且rsw10突变使一个保守的谷氨酸残基被赖氨酸取代。尽管RPI与许多生化途径密切相关,但培养基补充实验表明,可见表型是由嘧啶基糖核苷酸化合物生成缺陷导致的,最有可能是尿苷5'-二磷酸葡萄糖,它被认为是纤维素合酶的底物。核基因组中三个RPI序列中的两个位于细胞质中,而第三个具有推定的叶绿体转运序列。当在CaMV 35S启动子后表达时,编码两种细胞质酶的序列可以互补该突变,而将RSW10启动子区域与GUS报告基因融合表明该基因在许多地上组织以及根中都有表达。rsw10表型在根中突出可能反映了RSW10是该组织中唯一的胞质RPI,而编码质体RPI的基因表达相对较弱。然而,我们在根提取物中未检测到总RPI活性的降低。rsw10表型在根尖附近很突出,根尖处的细胞经历分裂、核内复制和细胞扩张,因此容易受到从头嘧啶合成受限的影响。这两种胞质RPI可能起源于一次古老的复制事件,它们目前的表达模式代表了原始祖先基因表达的亚功能化。