{"title":"mRNA translation from a unidirectional traffic perspective","authors":"Binil Shyam T V, Rati Sharma","doi":"arxiv-2312.12062","DOIUrl":null,"url":null,"abstract":"mRNA translation is a crucial process that leads to protein synthesis in\nliving cells. Therefore, it is a process that needs to work optimally for a\ncell to stay healthy and alive. With advancements in microscopy and novel\nexperimental techniques, a lot of the intricate details about the translation\nmechanism are now known. However, the why and how of this mechanism are still\nill understood, and therefore, is an active area of research. Theoretical\nstudies of mRNA translation typically view it in terms of the Totally\nAsymmetric Simple Exclusion Process or TASEP. Various works have used the TASEP\nmodel in order to study a wide range of phenomena and factors affecting\ntranslation, such as ribosome traffic on an mRNA under noisy (codon-dependent\nor otherwise) conditions, ribosome stalling, premature termination, ribosome\nreinitiation and dropoff, codon-dependent elongation and competition among mRNA\nfor ribosomes, among others. In this review, we relay the history and physics\nof the translation process in terms of the TASEP framework. In particular, we\ndiscuss the viability and evolution of this model and its limitations while\nalso formulating the reasons behind its success. Finally, we also identify gaps\nin the existing literature and suggest possible extensions and applications\nthat will lead to a better understanding of ribosome traffic on the mRNA.","PeriodicalId":501170,"journal":{"name":"arXiv - QuanBio - Subcellular Processes","volume":"12 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-12-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - QuanBio - Subcellular Processes","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2312.12062","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
mRNA translation is a crucial process that leads to protein synthesis in
living cells. Therefore, it is a process that needs to work optimally for a
cell to stay healthy and alive. With advancements in microscopy and novel
experimental techniques, a lot of the intricate details about the translation
mechanism are now known. However, the why and how of this mechanism are still
ill understood, and therefore, is an active area of research. Theoretical
studies of mRNA translation typically view it in terms of the Totally
Asymmetric Simple Exclusion Process or TASEP. Various works have used the TASEP
model in order to study a wide range of phenomena and factors affecting
translation, such as ribosome traffic on an mRNA under noisy (codon-dependent
or otherwise) conditions, ribosome stalling, premature termination, ribosome
reinitiation and dropoff, codon-dependent elongation and competition among mRNA
for ribosomes, among others. In this review, we relay the history and physics
of the translation process in terms of the TASEP framework. In particular, we
discuss the viability and evolution of this model and its limitations while
also formulating the reasons behind its success. Finally, we also identify gaps
in the existing literature and suggest possible extensions and applications
that will lead to a better understanding of ribosome traffic on the mRNA.