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数量:15 (7)

核糖体RNA的修改Intersubunit桥

短剑聚酯薄膜1*

1编辑部、生物化学:一个印度日报,印度

*通信:
短剑聚酯薄膜、编辑部、生物化学:一个印度日报》电子邮件::chemicalinformatics@chemjournals.org

收到:2021年11月10日;接受:2021年11月12日;发表:2021年11月30日

引用:聚酯薄膜c的核糖体RNA修改Intersubunit桥。印第安纳州j . 2021;15 (11):169。

文摘

核苷酸的变化中发现rRNA大约40年了,没有什么是有一些重要的意识的能力。消除的影响变化从一个巨大核糖体亚基intersubunit跨度(螺旋69)酵母的描绘。螺旋69有五个修改和连接一个和P网站图示。妨碍一到两个调整并不影响细胞改善,在任何情况下,失去三到五缓解背部的电池的发展和变化引起最广泛的违规行为在任何核糖体区域直到这一点。降低体内氨基酸腐蚀性融合率(25 - 60%),停止扩展密码子readthrough行动,更加突出对ribosome-based抗菌,减少rRNA水平(20-half),主要是由于快速的周转;并且改变了核糖体核糖体rna结构部分的显著影响。综上所述,发现建议这个子集rRNA的变化可以影响核糖体融合和协同能力。

关键词:

多功能核糖体;真核生物;结晶学;核苷酸;酿酒酵母

文摘:

核苷酸的变化中发现rRNA大约40年了,没有什么是有一些重要的意识的能力。消除的影响变化从一个巨大核糖体亚基intersubunit跨度(螺旋69)酵母的描绘。螺旋69有五个修改和连接一个和P网站图示。妨碍一到两个调整并不影响细胞改善,在任何情况下,失去三到五缓解背部的电池的发展和变化引起最广泛的违规行为在任何核糖体区域直到这一点。降低体内氨基酸腐蚀性融合率(25 - 60%),停止扩展密码子readthrough行动,更加突出对ribosome-based抗菌,减少rRNA水平(20-half),主要是由于快速的周转;并且改变了核糖体核糖体rna结构部分的显著影响。综上所述,发现建议这个子集rRNA的变化可以影响核糖体融合和协同能力。

作品简介:

有用的调查真核核糖体rna的核苷酸改变有了巨大的变化,因为核糖体科学的两个重要飞跃向前。一个是观察的两种主要类型rRNA调整假尿苷和2′-O-methylation (Nm)——是由site-explicit RNP机器叫做小核仁的RNP建筑(snRNPs)在真核生物和古菌。The snoRNA gives site-explicitness to the two sorts of adjustment by baseblending with the objective region. In a hereditarily manageable living resembling yeast, guide snoRNA articulation can be effectively hindered to forestall the improvement of a particular change (s). A guide of the rRNA alteration destinations, as well as the characters of the matching aide RNAs, are expected for the successful execution of this procedure. For Saccharomyces cerevisiae, the two essentials have been met.The accessibility of high-goal gem constructions of the ribosome, which permit relationship of adjustment maps with useful segments of the ribosome, is another key advancement that permits more powerful investigations of rRNA alterations. These progressions have made it conceivable to lead more precise rRNA alteration consumption examinations. The flow paper is important for another rush of examination that spotlights on changes to a multifunctional ribosomal span space. The altering snRNPs have a place with one of two major groups of snRNPs: the H/ACA box and the C/D box families. H/ACA snRNPs produce s, while C/D snRNPs produce Nm changes. The handling of rRNA forerunners is supported by a couple of snoRNAs. Each changing snoRNP has four center proteins that are shared by all individuals from the family, as well as a solitary, particular directing snoRNA. Exclusively, virtually all of the yeast guide snoRNAs have been decreased with no perceptible impact on cell development. These discoveries support the hypothesis that feasibility is free of rRNA changes. Notwithstanding, an enormous assemblage of examination recommends that the and Nm changes are very important on a worldwide scale, as seen underneath. They give off an impression of being found in each of the three realms of life's rRNAs, and their substance increments as phylogenetic intricacy increments. The practically significant rRNA areas of the ribosome are wealthy in changes. This state applies to the connection surfaces of both the little and enormous subunits, as well as the Peptidyl Transferase Center (PTC), the polypeptide leave burrow, and the regions that cooperate with mRNA and tRNA. This exploration centers around changes to a basic intersubunit span. At long last, overall interruption of and Nm development in rRNA has come about in close deadly development irregularities. Dynamic site transformations in the yeast snoRNP proteins that catalyze the alteration responses shut down these cycles.核磁共振安排考试已经展出,同时和纳米能解决RNA崩溃空间基础水平。假尿苷凝固的糖磷酸脊椎和进一步发展基础叠加在一个小巨大的方式。此外,给后续的贡献者网站创造氢键,从而协助平衡RNA-RNA或rna蛋白质通信。2′-哦目的地给一个核苷酸的甲基化更大的疏水性,从而协助分子间和分子内的通信。假设的思想和微不足道的试验研究模型这些标准的rna促使进步。特定的潜在影响进展rRNA空格或实际的核糖体在这一点上不清楚。调查的影响显式纳米和变化对rRNA工作是同样地处于早期阶段。固体发展违规在只有两个实例的杰出阻碍纳米调整。损失的变化从大肠杆菌rRNA的PTC地区(Um2552)抑制细胞发展和降低体外解释率达65%一个模型。阻碍甲基化在同类地区酿酒酵母(Um2918),相邻的网站(Gm2919),或两个地区显著阻碍细胞发展在其他模型中。最实用的缺陷带来的消除一个孤独的变化被发现在酵母PTC是一个圆。我们收集跟踪修改保存循环变化(2920)了体内的解释率20%,阻碍多核糖体发展一个疲惫的调查从这个区域6秒。审查,确定混合各种消耗显示小协同发展的好处,展示各种混合的变化调整核糖体结构以不同的方式。核糖体亚基之间的交集,解释发生的地方,看到很多真核核糖体rna的变化。 Numerous rRNA sections in these areas are associated with the making of intersubunit spans. A portion of these spanning structures associate with tRNA or other interpretation factors, inferring that changes to these extension districts might affect the interpretation cycle. In this paper, we check out the impacts of nucleotide changes on helix 69 (H69) in the huge subunit's space IV. Threes in E. coli, fours and one Nm in yeast, and fives and one Nm in people give off an impression of being normal around here. Positional preservation is saved in a couple of the changes. H69 interfaces with helix 44 (h44) in the little subunit (SSU) to deliver the intersubunit span B2a, as per crystallography. H44 is essential for the deciphering focus, and its association with H69 has first found in an E. coli ribosome crosslinking examination. Without any tRNA, cancellation of E. coli H69 modifies subunit affiliation, which is reliable with a job in subunit joining. H69 is effectively noticeable in a 5.5 design of Thermos thermophiles' 70S ribosome, however is confused in a 2.4 construction of Haloarcula marismortui's 50S subunit, inferring that it assumes a powerful part in subunit joining. H69 communicates with tRNAs in the flawless ribosome, recommending that it plays a capacity in tRNA movement and interpretation devotion. To be sure, a change on top of it region (U1915A) produced significant +1 frameshifting and stop密码子readthrough在新的遗传检查,显示H69在解释工作的忠诚。同时,低温电子显微镜检查连接H69 EF-G-catalyzed tRNA发展。H69核糖体重用因子的关系,根据结晶学(RRF)。在微生物,消除H69带来了普遍致命的聚合和肽放电阻抗。Asa结果,H69,其品种已经连接到各式各样的核糖体的能力。stem-circle地区预计对普通解释运动体外,显示突变检测大肠杆菌H69。一个反常的减少运动错过了马克在2260年主持匹配酵母,提议,这种改变可能是实用的意义。与另一个比较酵母2258,这是一个最特别的监控中发现的微生物,酵母,和人。这两个年代,以及第三个H69中同样发现,是由一个基本的蛋白质(RluD);在任何情况下,点RluD动态区发现的变化不需要混合的工作。 A核磁共振评估H69部分从大肠杆菌和人发现的进展产生一个小品种适应和解决基层RNA双工。11-nucleotide区域内,在酵母H69空间有五个变化,都是受保护的。的擦除snoRNA指导两个最监控年代(snR191)带来了一个小开发缺陷在过去的报告。我们表明,消除特定的混合H69修改从根本上减少细胞增殖,解释,和核糖体积累,以及修改核糖体的结构。

结论:

氨酰停靠站点的微生物是无差别的区域,和迫在眉睫的是解释。Gm2922出现在后期处理阶段,在27日的发展年代pre-rRNA,相对于其他2′-O-methylriboses上产生必要的记录。因此,真核生物一直site-explicit催化剂,催化甲基化对核糖体的核苷酸重要联盟和解释。

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