Department of Biological Sciences, Vanderbilt University, Nashville, Tennessee, United States of America.
PLoS One. 2012;7(3):e32500. doi: 10.1371/journal.pone.0032500. Epub 2012 Mar 5.
A major mechanism of translational regulation in response to a variety of stresses is mediated by phosphorylation of eIF2α to reduce delivery of initiator tRNAs to scanning ribosomes. For some mRNAs, often encoding a bZIP transcription factor, eIF2α phosphorylation leads to enhanced translation due to delayed reinitiation at upstream open reading frames. Dictyostelium cells possess at least three eIF2α kinases that regulate various portions of the starvation-induced developmental program. Cells possessing an eIF2α that cannot be phosphorylated (BS167) show abnormalities in growth and development. We sought to identify a bZIP protein in Dictyostelium whose production is controlled by the eIF2α regulatory system.
Cells disrupted in the bzpR gene had similar developmental defects as BS167 cells, including small entities, stalk defects, and reduced spore viability. β-galactosidase production was used to examine translation from mRNA containing the bzpR 5' UTR. While protein production was readily apparent and regulated temporally and spatially in wild type cells, essentially no β-galactosidase was produced in developing BS167 cells even though the lacZ mRNA levels were the same as those in wild type cells. Also, no protein production was observed in strains lacking IfkA or IfkB eIF2α kinases. GFP fusions, with appropriate internal controls, were used to directly demonstrate that the bzpR 5' UTR, possessing 7 uORFs, suppressed translation by 12 fold. Suppression occurred even when all but one uORF was deleted, and translational suppression was removed when the ATG of the single uORF was mutated.
The findings indicate that BzpR regulates aspects of the development program in Dictyostelium, serving as a downstream effector of eIF2α phosphorylation. Its production is temporally and spatially regulated by eIF2α phosphorylation by IfkA and IfkB and through the use of uORFs within the bzpR 5' UTR.
应对各种应激的翻译调控的一个主要机制是通过磷酸化 eIF2α 来减少起始 tRNA 向扫描核糖体的传递。对于某些 mRNA,通常编码 bZIP 转录因子,eIF2α 磷酸化会导致在上游开放阅读框处延迟重新起始,从而增强翻译。粘菌细胞至少拥有三种调节饥饿诱导发育程序各个部分的 eIF2α 激酶。细胞中存在不能被磷酸化的 eIF2α(BS167)会导致生长和发育异常。我们试图鉴定一种 bZIP 蛋白,该蛋白在粘菌中的产生受到 eIF2α 调节系统的控制。
bzpR 基因缺失的细胞具有与 BS167 细胞相似的发育缺陷,包括小实体、柄缺陷和孢子活力降低。β-半乳糖苷酶的产生用于检查含有 bzpR 5'UTR 的 mRNA 的翻译。虽然在野生型细胞中,蛋白质的产生很容易观察到,并在时间和空间上受到调节,但在发育中的 BS167 细胞中几乎没有产生β-半乳糖苷酶,尽管 lacZ mRNA 水平与野生型细胞相同。此外,在缺乏 IfkA 或 IfkB eIF2α 激酶的菌株中也没有观察到蛋白质的产生。带有适当内部对照的 GFP 融合物被用来直接证明 bzpR 5'UTR 具有 7 个 uORF,通过抑制翻译将其抑制 12 倍。即使删除了除一个 uORF 之外的所有 uORF,抑制作用仍然存在,并且当单个 uORF 的 ATG 发生突变时,翻译抑制作用被消除。
这些发现表明 BzpR 调节粘菌发育程序的各个方面,作为 eIF2α 磷酸化的下游效应物。它的产生受 IfkA 和 IfkB 的 eIF2α 磷酸化以及 bzpR 5'UTR 中 uORF 的时空调节。