Ivanov Ivaylo P, Wei Jiajie, Caster Stephen Z, Smith Kristina M, Michel Audrey M, Zhang Ying, Firth Andrew E, Freitag Michael, Dunlap Jay C, Bell-Pedersen Deborah, Atkins John F, Sachs Matthew S
School of Biochemistry and Cell Biology, University College Cork, Cork, Ireland.
Department of Biology, Texas A&M University, College Station, Texas, USA.
mBio. 2017 Jun 27;8(3):e00844-17. doi: 10.1128/mBio.00844-17.
and are homologs specifying transcription activators that drive the transcriptional response to amino acid limitation. The mRNA contains two upstream open reading frames (uORFs) in its >700-nucleotide (nt) 5' leader, and its expression is controlled at the level of translation in response to amino acid starvation. We used cell extracts and obtained data indicating that uORF1 and uORF2 are functionally analogous to uORF1 and uORF4, respectively, in controlling translation. We also found that the 5' region upstream of the main coding sequence of the mRNA extends for more than 700 nucleotides without any in-frame stop codon. For 100 homologs from Pezizomycotina and from selected Basidiomycota, 5' conserved extensions of the CPC1 reading frame are also observed. Multiple non-AUG near-cognate codons (NCCs) in the CPC1 reading frame upstream of uORF2, some deeply conserved, could potentially initiate translation. At least four NCCs initiated translation data were consistent with initiation at NCCs to produce N-terminally extended CPC1 isoforms. The pivotal role played by CPC1, combined with its translational regulation by uORFs and NCC utilization, underscores the emerging significance of noncanonical initiation events in controlling gene expression. There is a deepening and widening appreciation of the diverse roles of translation in controlling gene expression. A central fungal transcription factor, the best-studied example of which is GCN4, is crucial for the response to amino acid limitation. Two upstream open reading frames (uORFs) in the GCN4 mRNA are critical for controlling GCN4 synthesis. We observed that two uORFs in the corresponding mRNA appear functionally analogous to the GCN4 uORFs. We also discovered that, surprisingly, unlike GCN4, the CPC1 coding sequence extends far upstream from the presumed AUG start codon with no other in-frame AUG codons. Similar extensions were seen in homologs from many filamentous fungi. We observed that multiple non-AUG near-cognate codons (NCCs) in this extended reading frame, some conserved, initiated translation to produce longer forms of CPC1, underscoring the significance of noncanonical initiation in controlling gene expression.
[基因名称1]和[基因名称2]是同源物,它们指定转录激活因子,驱动对氨基酸限制的转录反应。[基因名称1]的mRNA在其大于700个核苷酸(nt)的5'前导序列中包含两个上游开放阅读框(uORF),并且其表达在翻译水平上受到氨基酸饥饿的调控。我们使用[细胞名称]细胞提取物并获得数据,表明[基因名称1]的uORF1和uORF2在控制翻译方面分别与[另一基因名称]的uORF1和uORF4功能相似。我们还发现,[基因名称1]mRNA主要编码序列上游的5'区域延伸超过700个核苷酸,没有任何框内终止密码子。对于来自粪壳菌纲和选定担子菌纲的100个[基因名称1]同源物,也观察到CPC1阅读框的5'保守延伸。uORF2上游的CPC1阅读框中的多个非AUG近同源密码子(NCC),有些是高度保守的,可能启动翻译。至少四个NCC启动了翻译,[实验相关内容]数据与在NCC处起始以产生N端延伸的CPC1异构体一致。CPC1发挥的关键作用,连同其通过uORF和NCC利用的翻译调控,强调了非经典起始事件在控制基因表达中日益重要的意义。人们对翻译在控制基因表达中的多种作用的认识正在不断深化和扩展。一种核心真菌转录因子,其中研究得最透彻的例子是[基因名称3],对于对氨基酸限制的反应至关重要。[基因名称3]mRNA中的两个上游开放阅读框(uORF)对于控制[基因名称3]的合成至关重要。我们观察到相应的[基因名称1]mRNA中的两个uORF在功能上似乎与[基因名称3]的uORF相似。我们还惊讶地发现,与[基因名称3]不同,CPC1编码序列从假定的AUG起始密码子向上游延伸很远,没有其他框内AUG密码子。在许多丝状真菌的同源物中也观察到类似的延伸。我们观察到这个延伸阅读框中的多个非AUG近同源密码子(NCC),有些是保守的,启动翻译以产生更长形式的CPC1,强调了非经典起始在控制基因表达中的重要性。