Literature DB >> 25662462

ChIP-seq and RNA-seq methods to study circadian control of transcription in mammals.

Joseph S Takahashi1, Vivek Kumar2, Prachi Nakashe3, Nobuya Koike3, Hung-Chung Huang3, Carla B Green3, Tae-Kyung Kim3.   

Abstract

Genome-wide analyses have revolutionized our ability to study the transcriptional regulation of circadian rhythms. The advent of next-generation sequencing methods has facilitated the use of two such technologies, ChIP-seq and RNA-seq. In this chapter, we describe detailed methods and protocols for these two techniques, with emphasis on their usage in circadian rhythm experiments in the mouse liver, a major target organ of the circadian clock system. Critical factors for these methods are highlighted and issues arising with time series samples for ChIP-seq and RNA-seq are discussed. Finally, detailed protocols for library preparation suitable for Illumina sequencing platforms are presented.
© 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Acetylation; ChIP-seq; Chromatin; Circadian; Histone; Methylation; RNA polymerase II; RNA-seq; Sequencing; Transcription

Mesh:

Substances:

Year:  2014        PMID: 25662462      PMCID: PMC4402199          DOI: 10.1016/bs.mie.2014.10.059

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  44 in total

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  14 in total

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5.  Cycling Transcriptional Networks Optimize Energy Utilization on a Genome Scale.

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7.  Circadian alignment of early onset caloric restriction promotes longevity in male C57BL/6J mice.

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8.  Novel transcriptional networks regulated by CLOCK in human neurons.

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