Mullen R T, Gifford D J
Department of Biological Sciences, University of Alberta, Edmonton, Canada.
Plant Mol Biol. 1997 Mar;33(4):593-604. doi: 10.1023/a:1005770724644.
Two full-length cDNAs encoding the glyoxysomal enzyme isocitrate lyase (ICL) were isolated from a lambda ZAP cDNA library prepared from megagametophyte mRNAs extracted from seeds imbibed at 30 degrees C for 8 days. The cDNAs, designated Ptbs ICL 8 and Ptbs ICL 12, have open reading frames of 1740 and 1719 bp, with deduced amino acid sequences of 580 and 573 residues, respectively. The predicted amino acid sequences of Ptbs ICL 8 and Ptbs ICL 12 exhibit a 79% identity with each other, and have a greater than 75% identity with ICLs from various angiosperm species. The C-termini of Ptbs ICL 8 and Ptbs ICL 12 terminate with the tripeptide Ser-Arg-Met and Ala-Arg-Met, respectively, both being conserved variants of the type 1 peroxisomal targeting signal. RNA blot and slot analysis revealed that Ptbs ICL 8 and Ptbs ICL 12 mRNAs were present at low levels in the megagametophyte of the mature and stratified seeds, and that the level of both transcripts increased markedly upon seed germination. Protein blot analysis indicated that the steady-state level of ICL was low in the mature and stratified seed, then increased rapidly upon seed germination, peaking at around 8-10 days after imbibition (DAI). Changes in the level of ICL activity in cell-free extracts was similar to the steady-state protein content with the exception that ICL activity was not detected in megagametophyte extracts of mature or stratified seeds. From 10-12 DAI when the megagametophyte tissue senesced, ICL activity decreased rapidly to near undetectable levels. In contrast, steady-state levels of ICL protein and mRNA remained relatively constant during megagametophyte senescence. In vivo synthesis of ICL protein was measured to shed light on these differences. ICL immunoselected from [(35)S]-methionine labelled proteins indicated that ICL was synthesized at very low levels during megagametophyte senescence. Together, the results show that loblolly pine ICL gene expression is complex. While temporal regulation appears to be primarily transcriptional, it also involves a number of post-transcriptional processes including at least one translational and/or post-translational mechanism.
从一个λZAP cDNA文库中分离出了两个编码乙醛酸循环体酶异柠檬酸裂解酶(ICL)的全长cDNA,该文库是用从在30℃吸水8天的种子中提取的雌配子体mRNA构建的。这两个cDNA分别命名为Ptbs ICL 8和Ptbs ICL 12,开放阅读框分别为1740和1719 bp,推导的氨基酸序列分别为580和573个残基。Ptbs ICL 8和Ptbs ICL 12的预测氨基酸序列彼此间有79%的同一性,并且与来自各种被子植物物种的ICL有超过75%的同一性。Ptbs ICL 8和Ptbs ICL 12的C末端分别以三肽Ser-Arg-Met和Ala-Arg-Met终止,二者均为1型过氧化物酶体靶向信号的保守变体。RNA印迹和狭缝分析表明,Ptbs ICL 8和Ptbs ICL 12的mRNA在成熟和层积种子的雌配子体中含量较低,且在种子萌发时这两种转录本的水平均显著增加。蛋白质印迹分析表明,ICL的稳态水平在成熟和层积种子中较低,在种子萌发时迅速增加,在吸水后8 - 10天左右达到峰值。无细胞提取物中ICL活性水平的变化与稳态蛋白质含量相似,不同之处在于在成熟或层积种子的雌配子体提取物中未检测到ICL活性。从吸水后10 - 12天雌配子体组织衰老开始,ICL活性迅速下降至几乎检测不到的水平。相比之下,在雌配子体衰老过程中,ICL蛋白质和mRNA的稳态水平保持相对恒定。通过测量ICL蛋白质的体内合成来揭示这些差异。从[³⁵S]-甲硫氨酸标记的蛋白质中免疫选择的ICL表明,在雌配子体衰老期间ICL的合成水平非常低。总之,结果表明火炬松ICL基因的表达是复杂的。虽然时间调控似乎主要是转录水平的,但它也涉及许多转录后过程,包括至少一种翻译和/或翻译后机制。