Ni W., Trelease R. N.
Department of Botany, Arizona State University, Tempe, Arizona 85287-1601.
Plant Cell. 1991 Jul;3(7):737-744. doi: 10.1105/tpc.3.7.737.
We reported previously that expression of the five tetrameric catalase isozymes during postgerminative growth of cotton seedings was a consequence of interactions between two subunits (SU 1 and SU 2) temporally synthesized from two distinct catalase genes. In this study, we focused on the regulation of the expression of these two catalase subunits during the changeover from glyoxysomal to leaf-type peroxisomal metabolism. The steady-state level of glyoxysomal SU 1 protein (present in 12-hour-old seeds) increased through day 3 and then declined linearly through day 6, whereas SU 2 protein (first detected in 24-hour-old seeds) increased continuously through day 6. The time courses for steady-state levels of the mRNAs encoding these two subunits revealed two clearly separated peaks: the first at day 1 (SU 1) and the other at day 4 (SU 2). Accumulation of these mRNAs preceded the accumulation of their corresponding proteins by at least 24 hours, suggesting temporal, pretranslational regulation of synthesis of both subunits. Results from run-on transcriptional assays with isolated nuclei, however, revealed that transcripts encoding both subunits were synthesized together on days 1 through 5. Hence, it appears that the accumulations of SU 1 and SU 2 mRNAs are controlled primarily at the post-transcriptional level, which has not been reported for catalase or any other eukaryotic peroxisomal enzymes. The accumulation of SU 1 mRNA is not light dependent, whereas the accumulation of SU 2 mRNA, which directs synthesis of the predominant subunit comprising the leaf-type peroxisomal isozyme, occurs only after exposure of seedlings to light.
我们之前报道过,棉花幼苗发芽后生长过程中五种四聚体过氧化氢酶同工酶的表达是由两个亚基(SU 1和SU 2)之间相互作用的结果,这两个亚基是由两个不同的过氧化氢酶基因在不同时间合成的。在本研究中,我们聚焦于从乙醛酸循环体代谢转变为叶片型过氧化物酶体代谢过程中这两个过氧化氢酶亚基表达的调控。乙醛酸循环体SU 1蛋白(存在于12小时龄的种子中)的稳态水平在第3天之前升高,然后在第6天之前呈线性下降,而SU 2蛋白(首次在24小时龄的种子中检测到)在第6天之前持续增加。编码这两个亚基的mRNA稳态水平的时间进程显示出两个明显分开的峰值:第一个在第1天(SU 1),另一个在第4天(SU 2)。这些mRNA的积累比其相应蛋白质的积累至少提前24小时,这表明两个亚基的合成存在时间上的转录前调控。然而,用分离的细胞核进行的连续转录分析结果显示,编码这两个亚基的转录本在第1天至第5天一起合成。因此,似乎SU 1和SU 2 mRNA的积累主要在转录后水平受到控制,这在过氧化氢酶或任何其他真核过氧化物酶体酶中尚未有报道。SU 1 mRNA的积累不依赖于光,而指导叶片型过氧化物酶体同工酶主要亚基合成的SU 2 mRNA的积累仅在幼苗暴露于光后才发生。