Original Research Open Access Logo

Study on predicting highy expressed genes for Escherichia coli based on mRNA microarray data

Nam Tri Vo 1
Nghia Trung Pham 1
Nhat Ha Minh Truong 1
Thuoc Linh Tran 2
Hoang Duc Nguyen 1, *
  1. Center for Bioscience and Biotechnology, University of Science, VNU-HCMC, Vietnam
  2. Faculty of Biology -Biotechnology, University of Science, VNU-HCMC, Vietnam
Correspondence to: Hoang Duc Nguyen, Center for Bioscience and Biotechnology, University of Science, VNU-HCMC, Vietnam. Email: ndhoang@hcmus.edu.vn.
Volume & Issue: Vol. 5 No. 2 (2021) | Page No.: 1068-1077 | DOI: 10.32508/stdjns.v5i2.945
Published: 2021-04-30

Online metrics


Statistics from the website

  • Abstract Views: 3229
  • Galley Views: 459

Statistics from Dimensions

This article is published with open access by Viet Nam National University Ho Chi Minh City, Viet Nam. This article is distributed under the terms of the Creative Commons Attribution License (CC-BY 4.0) which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.

Abstract

Highly expressed genes [HEG] are genes available in the organism, which carry the preferred codons for the expression system. Identifying HEG helps to find preferred codons and use them in the gene optimization to express target proteins. Currently, HEG-DB is the only database storing HEG data of many strains of microorganisms, but the data is not updated and maintained. Therefore, our research is carried out to predict HEG in the E. coli K-12 MG1655 strain based on reference sets that are the mostly used ribosomal protein coding genes and genes with high transcription levels from microarray data proposed by the research. Next, the results of HEG from the two above reference sets, HEG-RP and HEG-mRNA, were compared. Finally, we analyzed and compared the HEG that the project predicted with HEG from HEG-DB database. The results from RP and 100-mRNA reference sets were completely identical and were better than data from HEG-DB in the number of HEGs, CAI values and the number of genes contributing to important metabolic pathways. The results showed that it was possible to use reference sets from mRNA microarray data instead of ribosomal protein reference sets in HEG prediction.

Comments