首页> 外文期刊>Plant physiology >Two Arabidopsis Loci Encode Novel Eukaryotic Initiation Factor 4E Isoforms That Are Functionally Distinct from the Conserved Plant Eukaryotic Initiation Factor 4E~(1[W][OPEN])
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Two Arabidopsis Loci Encode Novel Eukaryotic Initiation Factor 4E Isoforms That Are Functionally Distinct from the Conserved Plant Eukaryotic Initiation Factor 4E~(1[W][OPEN])

机译:两个拟南芥基因座编码新功能的真核生物起始因子4E同保守植物真核生物起始因子4E〜(1 [W] [OPEN])

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摘要

Canonical translation initiation in eukaryotes begins with the Eukaryotic Initiation Factor 4F (eIF4F) complex, made up of eIF4E, which recognizes the 7-methylguanosine cap of messenger RNA, and eIF4G, which serves as a scaffold to recruit other translation initiation factors that ultimately assemble the 80S ribosome. Many eukaryotes have secondary EIF4E genes with divergent properties. The model plant Arabidopsis (Arabidopsis thaliana) encodes two such genes in tandem loci on chromosome 1, EIF4E1B (At1g29550) and EIF4E1C (At1g29590). This work identifies EIF4E1B/EIF4E1C-type genes as a Brassicaceae-specific diverged form of EIF4E. There is little evidence for EIF4E1C gene expression; however, the EIF4E1B gene appears to be expressed at low levels in most tissues, though microarray and RNA Sequencing data support enrichment in reproductive tissue. Purified recombinant eIF4E1b and eIF4E1c proteins retain cap-binding ability and form functional complexes in vitro with eIF4G. The eIF4E1b/eIF4E1c-type proteins support translation in yeast (Saccharomyces cerevisiae) but promote translation initiation in vitro at a lower rate compared with eIF4E. Findings from surface plasmon resonance studies indicate that eIF4E1b and eIF4E1c are unlikely to bind eIF4G in vivo when in competition with eIF4E. This study concludes that eIF4E1b/eIF4E1c-type proteins, although bona fide cap-binding proteins, have divergent properties and, based on apparent limited tissue distribution in Arabidopsis, should be considered functionally distinct from the canonical plant eIF4E involved in translation initiation.
机译:真核生物的规范翻译起始始于真核起始因子4F(eIF4F)复合物,该复合物由识别信使RNA的7-甲基鸟苷帽的eIF4E和作为募集其他翻译起始因子的支架的eIF4G组成80S核糖体。许多真核生物具有具有不同特性的次要EIF4E基因。模型植物拟南芥(Arabidopsis thaliana)在1号染色体EIF4E1B(At1g29550)和EIF4E1C(At1g29590)的串联基因座中编码两个这样的基因。这项工作确定EIF4E1B / EIF4E1C型基因为十字花科特定的EIF4E发散形式。 EIF4E1C基因表达的证据很少。然而,尽管微阵列和RNA测序数据支持生殖组织中的富集,但EIF4E1B基因在大多数组织中似乎均以低水平表达。纯化的重组eIF4E1b和eIF4E1c蛋白保留了帽结合能力,并在体外与eIF4G形成功能性复合物。 eIF4E1b / eIF4E1c型蛋白支持酵母(Saccharomyces cerevisiae)中的翻译,但与eIF4E相比,在体外以较低的速率促进翻译起始。表面等离振子共振研究的结果表明,eIF4E1b和eIF4E1c与eIF4E竞争时,不太可能在体内结合eIF4G。这项研究得出的结论是,尽管真正的帽结合蛋白具有eIF4E1b / eIF4E1c型蛋白,但它们具有不同的性质,并且基于拟南芥中明显有限的组织分布,应将其视为功能上与参与翻译起始的规范植物eIF4E不同。

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