Vegetable Crops Department, University of Florida, Gainesville, FL 32611.
Proc Natl Acad Sci U S A. 1986 Dec;83(23):9099-103. doi: 10.1073/pnas.83.23.9099.
Two differentially expressed genes encode isoenzymes of sucrose synthase in Zea mays. A clone of the shrunken 1 (Sh1) locus, the structural gene for the major endosperm form of sucrose synthase, was used to isolate a genomic clone of constitutive sucrose synthase (Css), the structural gene for the isoenzyme expressed in embryo and other tissues. The Css clone was positively identified by RNA blot analysis of RNA from wild type and a sh1 deletion stock and by analysis of the in vitro translation product of hybrid-selected mRNA. Southern blot analysis of DNA from monosomic plants derived from an r-x1 stock, coupled with restriction fragment length polymorphism mapping, placed the Css gene 32 map units from Sh1 on chromosome 9. In seedling tissues, Css mRNA is present at higher levels than Sh1 mRNA. Expression of both Sh1 and Css in root tissue is enhanced by anaerobic conditions, although Css is induced to a lesser extent than is Sh1. Thus, Css appears to be expressed constitutively, whereas Sh1 is expressed at high levels only in response to specific developmental and environmental stimuli.
两个差异表达的基因编码玉米中蔗糖合酶的同工酶。使用一个 shriken1 (Sh1) 基因座的克隆,该基因座是主要胚乳形式蔗糖合酶的结构基因,来分离组成型蔗糖合酶(Css)的基因组克隆,该基因座是在胚胎和其他组织中表达的同工酶的结构基因。通过对来自野生型和 sh1 缺失品系的 RNA 的 RNA 印迹分析以及对杂交选择 mRNA 的体外翻译产物的分析,对 Css 克隆进行了阳性鉴定。来自 r-x1 品系的单体植物的 DNA 的 Southern 印迹分析,加上限制片段长度多态性作图,将 Css 基因定位于第 9 号染色体上,距离 Sh1 基因 32 个图谱单位。在幼苗组织中,Css mRNA 的含量高于 Sh1 mRNA。根组织中 Sh1 和 Css 的表达均受厌氧条件的增强,尽管 Css 的诱导程度低于 Sh1。因此,Css 似乎是组成型表达的,而 Sh1 仅在响应特定的发育和环境刺激时才高水平表达。