Literature DB >> 24365110

A new microarray platform for whole-genome expression profiling of Mycobacterium tuberculosis.

Balaji Venkataraman1, Madavan Vasudevan2, Amita Gupta3.   

Abstract

Microarrays have allowed gene expression profiling to progress from the gene level to the genome level, and oligonucleotide microarrays have become the platform of choice for large-scale, targeted gene expression studies. cDNA arrays and spotted oligonucleotide arrays have gradually given way to in situ synthesized oligonucleotide-based DNA microarrays for whole-genome expression profiling. With the identification of new coding and regulatory sequences, it is imperative that microarrays be updated to enable more complete expression profiling of genomes. We report here a new in situ synthesized oligonucleotide-based microarray platform for Mycobacterium tuberculosis that has been updated for the latest genome information and incorporates hitherto unannotated genes with described biological functions. This microarray has greater coverage of mycobacterial genes than any other array reported to date. We have also evaluated different labeled-target preparation methods and hybridization conditions for this new microarray to obtain high quality data and reproducible results. The new design has been rigorously validated for its specificity and performance using samples isolated from mycobacteria grown under different environment conditions. Further, the quality of the generated data has been compared with published data and is superior to that obtained using spotted oligonucleotide microarrays.
Copyright © 2013 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  M. tuberculosis; Microarray; RNA amplification; Whole genome expression profiling

Mesh:

Year:  2013        PMID: 24365110     DOI: 10.1016/j.mimet.2013.12.009

Source DB:  PubMed          Journal:  J Microbiol Methods        ISSN: 0167-7012            Impact factor:   2.363


  5 in total

1.  HigB1 Toxin in Mycobacterium tuberculosis Is Upregulated During Stress and Required to Establish Infection in Guinea Pigs.

Authors:  Arun Sharma; Kalpana Sagar; Neeraj Kumar Chauhan; Balaji Venkataraman; Nidhi Gupta; Tannu Priya Gosain; Nikhil Bhalla; Ramandeep Singh; Amita Gupta
Journal:  Front Microbiol       Date:  2021-11-30       Impact factor: 5.640

2.  Mycobacterium tuberculosis WhiB3 Responds to Vacuolar pH-induced Changes in Mycothiol Redox Potential to Modulate Phagosomal Maturation and Virulence.

Authors:  Mansi Mehta; Raju S Rajmani; Amit Singh
Journal:  J Biol Chem       Date:  2015-12-04       Impact factor: 5.157

3.  Co-expression network analysis of toxin-antitoxin loci in Mycobacterium tuberculosis reveals key modulators of cellular stress.

Authors:  Amita Gupta; Balaji Venkataraman; Madavan Vasudevan; Kiran Gopinath Bankar
Journal:  Sci Rep       Date:  2017-07-19       Impact factor: 4.379

4.  Redox-dependent condensation of the mycobacterial nucleoid by WhiB4.

Authors:  Manbeena Chawla; Saurabh Mishra; Kushi Anand; Pankti Parikh; Mansi Mehta; Manika Vij; Taru Verma; Parul Singh; Kishor Jakkala; H N Verma; Parthasarathi AjitKumar; Munia Ganguli; Aswin Sai Narain Seshasayee; Amit Singh
Journal:  Redox Biol       Date:  2018-08-13       Impact factor: 10.787

5.  Identification of key candidate targets and pathways for the targeted treatment of leukemia stem cells of chronic myelogenous leukemia using bioinformatics analysis.

Authors:  Huayao Li; Lijuan Liu; Jing Zhuang; Cun Liu; Chao Zhou; Jing Yang; Chundi Gao; Gongxi Liu; Changgang Sun
Journal:  Mol Genet Genomic Med       Date:  2019-08-02       Impact factor: 2.183

  5 in total

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