Literature DB >> 31588338

Methods for the analysis of transcriptome dynamics.

Daniela F Rodrigues1, Vera M Costa1, Ricardo Silvestre2,3, Maria L Bastos1, Félix Carvalho1.   

Abstract

The transcriptome is the complete set of transcripts in a cell or tissue and includes ribosomal RNA (rRNA), messenger RNA (mRNA), transfer RNA (tRNA), and regulatory noncoding RNA. At steady-state, the transcriptome results from a compensatory variation of the transcription and decay rate to maintain the RNA concentration constant. RNA transcription constitutes the first stage in gene expression, and thus is a major and primary mode of gene expression control. Nevertheless, regulation of RNA decay is also a key factor in gene expression control, involving either selective RNA stabilization or enhanced degradation. Transcriptome analysis allows the identification of gene expression alterations, providing new insights regarding the pathways and mechanisms involved in physiological and pathological processes. Upon perturbation of cell homeostasis, rapid changes in gene expression are required to adapt to new conditions. Thus, to better understand the regulatory mechanisms associated with gene expression alterations, it is vital to acknowledge the relative contribution of RNA synthesis and decay to the transcriptome. To the toxicology field, the study of gene expression regulation mechanisms can help identify the early and mechanistic relevant cellular events associated with a particular response. This review aims to provide a critical comparison of the available methods used to analyze the contribution of RNA transcription and decay to gene expression dynamics. Notwithstanding, an integration of the data obtained is necessary to understand the entire repercussions of gene transcription changes at a system-level. Thus, a brief overview of the methods available for the integration and analysis of the data obtained from transcriptome analysis will also be provided. This journal is © The Royal Society of Chemistry 2019.

Year:  2019        PMID: 31588338      PMCID: PMC6764467          DOI: 10.1039/c9tx00088g

Source DB:  PubMed          Journal:  Toxicol Res (Camb)        ISSN: 2045-452X            Impact factor:   3.524


  111 in total

1.  Nuclear run-on assays: assessing transcription by measuring density of engaged RNA polymerases.

Authors:  K Hirayoshi; J T Lis
Journal:  Methods Enzymol       Date:  1999       Impact factor: 1.600

2.  The MIQE guidelines: minimum information for publication of quantitative real-time PCR experiments.

Authors:  Stephen A Bustin; Vladimir Benes; Jeremy A Garson; Jan Hellemans; Jim Huggett; Mikael Kubista; Reinhold Mueller; Tania Nolan; Michael W Pfaffl; Gregory L Shipley; Jo Vandesompele; Carl T Wittwer
Journal:  Clin Chem       Date:  2009-02-26       Impact factor: 8.327

3.  The CTD code.

Authors:  Stephen Buratowski
Journal:  Nat Struct Biol       Date:  2003-09

Review 4.  Structural basis of transcription elongation.

Authors:  Fuensanta W Martinez-Rucobo; Patrick Cramer
Journal:  Biochim Biophys Acta       Date:  2012-09-13

5.  Nucleosomes are context-specific, H2A.Z-modulated barriers to RNA polymerase.

Authors:  Christopher M Weber; Srinivas Ramachandran; Steven Henikoff
Journal:  Mol Cell       Date:  2014-03-06       Impact factor: 17.970

6.  Re-utilization of pyrimidine nucleotides during rat liver regeneration.

Authors:  E N Nikolov; M D Dabeva
Journal:  Biochem J       Date:  1985-05-15       Impact factor: 3.857

Review 7.  Defining mechanisms that regulate RNA polymerase II transcription in vivo.

Authors:  Nicholas J Fuda; M Behfar Ardehali; John T Lis
Journal:  Nature       Date:  2009-09-10       Impact factor: 49.962

8.  Genome-wide determination of RNA stability reveals hundreds of short-lived noncoding transcripts in mammals.

Authors:  Hidenori Tani; Rena Mizutani; Kazi Abdus Salam; Keiko Tano; Kenichi Ijiri; Ai Wakamatsu; Takao Isogai; Yutaka Suzuki; Nobuyoshi Akimitsu
Journal:  Genome Res       Date:  2012-02-27       Impact factor: 9.043

9.  Fluorescent-increase kinetics of different fluorescent reporters used for qPCR depend on monitoring chemistry, targeted sequence, type of DNA input and PCR efficiency.

Authors:  Jan M Ruijter; Peter Lorenz; Jari M Tuomi; Michael Hecker; Maurice J B van den Hoff
Journal:  Mikrochim Acta       Date:  2014-01-14       Impact factor: 5.833

10.  ChIP-nexus enables improved detection of in vivo transcription factor binding footprints.

Authors:  Qiye He; Jeff Johnston; Julia Zeitlinger
Journal:  Nat Biotechnol       Date:  2015-03-09       Impact factor: 54.908

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  1 in total

1.  Thioguanosine Conversion Enables mRNA-Lifetime Evaluation by RNA Sequencing Using Double Metabolic Labeling (TUC-seq DUAL).

Authors:  Catherina Gasser; Isabel Delazer; Eva Neuner; Katharina Pascher; Karl Brillet; Sarah Klotz; Lukas Trixl; Maximilian Himmelstoß; Eric Ennifar; Dietmar Rieder; Alexandra Lusser; Ronald Micura
Journal:  Angew Chem Int Ed Engl       Date:  2020-02-28       Impact factor: 15.336

  1 in total

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