Prosdocimi Francisco, Zamudio Gabriel S, Palacios-Pérez Miryam, Torres de Farias Sávio, V José Marco
Laboratório de Biologia Teórica e de Sistemas, Instituto de Bioquímica Médica Leopoldo de Meis, Universidade Federal do Rio de Janeiro, Rio de Janeiro 21.941-902, Brazil.
Theoretical Biology Group, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México, Ciudad Universitaria, CDMX 04510, Mexico.
Life (Basel). 2020 Aug 5;10(8):134. doi: 10.3390/life10080134.
The peptidyl transferase center (PTC) is the catalytic center of the ribosome and forms part of the 23S ribosomal RNA. The PTC has been recognized as the earliest ribosomal part and its origins embodied the First Universal Common Ancestor (FUCA). The PTC is frequently assumed to be highly conserved along all living beings. In this work, we posed the following questions: (i) How many 100% conserved bases can be found in the PTC? (ii) Is it possible to identify clusters of informationally linked nucleotides along its sequence? (iii) Can we propose how the PTC was formed? (iv) How does sequence conservation reflect on the secondary and tertiary structures of the PTC? Aiming to answer these questions, all available complete sequences of 23S ribosomal RNA from Bacteria and Archaea deposited on GenBank database were downloaded. Using a sequence bait of 179 bp from the PTC of , we performed an optimum pairwise alignment to retrieve the PTC region from 1424 filtered 23S rRNA sequences. These PTC sequences were multiply aligned, and the conserved regions were assigned and observed along the primary, secondary, and tertiary structures. The PTC structure was observed to be more highly conserved close to the adenine located at the catalytical site. Clusters of interrelated, co-evolving nucleotides reinforce previous assumptions that the PTC was formed by the concatenation of proto-tRNAs and important residues responsible for its assembly were identified. The observed sequence variation does not seem to significantly affect the 3D structure of the PTC ribozyme.
肽基转移酶中心(PTC)是核糖体的催化中心,是23S核糖体RNA的一部分。PTC被认为是最早的核糖体部分,其起源体现了第一个普遍共同祖先(FUCA)。人们通常认为PTC在所有生物中都高度保守。在这项工作中,我们提出了以下问题:(i)在PTC中可以发现多少个100%保守的碱基?(ii)是否有可能在其序列中识别出信息相连的核苷酸簇?(iii)我们能否提出PTC是如何形成的?(iv)序列保守性如何反映在PTC的二级和三级结构上?为了回答这些问题,我们下载了GenBank数据库中所有可用的细菌和古菌23S核糖体RNA的完整序列。使用来自[具体物种]PTC的179 bp序列诱饵,我们进行了最优成对比对,以从1424条经过筛选的23S rRNA序列中检索PTC区域。对这些PTC序列进行多重比对,并沿着一级、二级和三级结构确定和观察保守区域。观察到PTC结构在靠近催化位点的腺嘌呤处更为高度保守。相互关联、共同进化的核苷酸簇强化了先前的假设,即PTC是由原始tRNA连接形成的,并确定了负责其组装的重要残基。观察到的序列变异似乎并未显著影响PTC核酶的三维结构。