Takahashi Y, Kusaba M, Hiraoka Y, Nagata T
Department of Biology, Faculty of Science, University of Tokyo, Japan.
Plant J. 1991 Nov;1(3):327-32. doi: 10.1046/j.1365-313x.1991.t01-2-00999.x.
The auxin-regulated par gene from tobacco mesophyll protoplasts was characterized in detail to deduce its possible function. An homology search of the par gene in the NBRF databases revealed that the par gene has homology to the stringent starvation protein (ssp) gene of Escherichia coli, which is induced under starved conditions and binds in an equimolar ratio to a holoenzyme of RNA polymerase. Hence, it is supposed that the par gene product could play a similar role to that of ssp. Although sequence homology of the par gene to the Gmhsp 26-A gene from soybean was observed, both genes were shown to respond differently to plant hormones and stresses. Gmhsp 26-A is induced by heat shock, 2,4-dichlorophenoxyacetic acid (2,4-D), cytokinin and abscisic acid (ABA), whereas the par gene was induced only by auxins. Furthermore, cycloheximide treatment prevents 2,4-D-mediated accumulation of Gmhsp 26-A mRNA, but not that of par mRNA. Both par and Gmhsp 26-A respond to CdCl2, but splicing of the par pre-mRNA proceeded in a normal way, whereas splicing off the Gmhsp 26-A pre-mRNA was inhibited. Hence, the par and Gmhsp 26-A genes should have a common ancestor, but have evolved in different directions. Detailed time-course experiments confirmed that the par gene was induced immediately after the addition of auxin and expressed upon the initiation of meristematic activity in tobacco mesophyll protoplasts. As the par gene was induced by the sole treatment of cycloheximide, it was proposed that the par gene belongs to a category of 'superinduction' genes.(ABSTRACT TRUNCATED AT 250 WORDS)
为了推断生长素调节的烟草叶肉原生质体par基因的可能功能,对其进行了详细表征。在NBRF数据库中对par基因进行同源性搜索发现,该par基因与大肠杆菌的严紧饥饿蛋白(ssp)基因具有同源性,后者在饥饿条件下被诱导,并以等摩尔比与RNA聚合酶全酶结合。因此,推测par基因产物可能发挥与ssp类似的作用。尽管观察到par基因与大豆的Gmhsp 26 - A基因有序列同源性,但这两个基因对植物激素和胁迫的反应不同。Gmhsp 26 - A受热激、2,4 -二氯苯氧乙酸(2,4 - D)、细胞分裂素和脱落酸(ABA)诱导,而par基因仅受生长素诱导。此外,环己酰亚胺处理可阻止2,4 - D介导的Gmhsp 26 - A mRNA积累,但不影响par mRNA的积累。par和Gmhsp 26 - A都对CdCl2有反应,但par前体mRNA的剪接正常进行,而Gmhsp 26 - A前体mRNA的剪接受到抑制。因此,par和Gmhsp 26 - A基因应有一个共同的祖先,但已朝着不同方向进化。详细的时间进程实验证实,在添加生长素后par基因立即被诱导,并在烟草叶肉原生质体分生组织活性开始时表达。由于par基因仅经环己酰亚胺处理就被诱导,因此推测par基因属于“超诱导”基因类别。(摘要截短至250字)