نتایج جستجو برای: codon usage

تعداد نتایج: 114780  

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه علم و فرهنگ 1393

هورمون fsh ماهی عضوی از خانواده گنادوتروپین ها است که از غده هیپوفیز ماهی ترشح می شود. ساختمان این هورمون از دو زیرواحد ? و ? تشکیل شده است که به صورت غیرکووالان به یکدیگر متصل شده اند. این هورمون در تنظیم فرآیندهای ضروری تولیدمثل مانند گامتوژنز و رشد فولیکولار در ماهی نقش دارد. از مزایای تولید نوترکیب هورمون fsh می توان به اطمینان از عدم وجود آلودگی با سایر هورمون های گلیکوپروتئینی هیپوفیز و ه...

Journal: :The EMBO journal 2014
Dominique Chu Eleanna Kazana Noémie Bellanger Tarun Singh Mick F Tuite Tobias von der Haar

Synonymous codons encode the same amino acid, but differ in other biophysical properties. The evolutionary selection of codons whose properties are optimal for a cell generates the phenomenon of codon bias. Although recent studies have shown strong effects of codon usage changes on protein expression levels and cellular physiology, no translational control mechanism is known that links codon us...

Journal: :Molecular biology and evolution 2018
N Galtier C Roux M Rousselle J Romiguier E Figuet S Glémin N Bierne L Duret

Selection on codon usage bias is well documented in a number of microorganisms. Whether codon usage is also generally shaped by natural selection in large organisms, despite their relatively small effective population size (Ne), is unclear. In animals, the population genetics of codon usage bias has only been studied in a handful of model organisms so far, and can be affected by confounding, no...

2016
Sushanta Deb Surajit Basak

Paenibacillus sp. 32O-W, which is attributed for biodesulfurization of petroleum, has 56.34% genomic G+C content. Correspondence analysis on Relative Synonymous Codon Usage (RSCU) of the Paenibacillus sp. 32O-W genome has revealed the two different trends of codon usage variation. Two sets of genes have been identified representing the two distinct pattern of codon usage in this bacterial genom...

Journal: :Bioinformatics 2012
Paulo Gaspar José Luís Oliveira Jörg Frommlet Manuel A. S. Santos Gabriela R. Moura

UNLABELLED Numerous software applications exist to deal with synthetic gene design, granting the field of heterologous expression a significant support. However, their dispersion requires the access to different tools and online services in order to complete one single project. Analyzing codon usage, calculating codon adaptation index (CAI), aligning orthologs and optimizing genes are just a fe...

2012
Manoj Kumar Yadav D Swati

UNLABELLED Codon usage bias (CUB) is an omnipresent phenomenon, which occurs in nearly all organisms. Previous studies of codon bias in Plasmodium species were based on a limited dataset. This study uses whole genome datasets for comparative genome analysis of six Plasmodium species using CUB and other related methods for the first time. Codon usage bias, compositional variation in translated a...

2017
Paweł Błażej Dorota Mackiewicz Małgorzata Wnętrzak Paweł Mackiewicz

There are two main forces that affect usage of synonymous codons: directional mutational pressure and selection. The effectiveness of protein translation is usually considered as the main selectional factor. However, biased codon usage can also be a byproduct of a general selection at the amino acid level interacting with nucleotide replacements. To evaluate the validity and strength of such an...

Journal: :DNA Research: An International Journal for Rapid Publication of Reports on Genes and Genomes 2008
Haruo Suzuki Celeste J. Brown Larry J. Forney Eva M. Top

Synonymous codon usage varies both between organisms and among genes within a genome, and arises due to differences in G + C content, replication strand skew, or gene expression levels. Correspondence analysis (CA) is widely used to identify major sources of variation in synonymous codon usage among genes and provides a way to identify horizontally transferred or highly expressed genes. Four me...

2015
Arif Uddin Tarikul Huda Mazumder Monisha Nath Choudhury Supriyo Chakraborty

BACKGROUND Mitochondrial ND gene, which encodes NADH dehydrogenase, is the first enzyme of the mitochondrial electron transport chain. Leigh syndrome, a neurodegenerative disease caused by mutation in the ND2 gene (T4681C), is associated with bilateral symmetric lesions in basal ganglia and subcortical brain regions. Therefore, it is of interest to analyze mitochondrial DNA to glean information...

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