NAD-seq for profiling the NAD+ capped transcriptome of Arabidopsis thaliana
Summary: Eukaryotic RNAs can be modified with a non-canonical 5′ nicotinamide adenine dinucleotide (NAD+) cap. NAD-seq identifies transcriptome-wide NAD+ capped RNAs. NAD-seq takes advantage of click chemistry to allow the capture of NAD+ capped RNAs. Unlike other approaches, NAD-seq does not requir...
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Elsevier
2021
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oai:doaj.org-article:e3b2951872f144749e381e62ce4ac6862021-11-14T04:35:35ZNAD-seq for profiling the NAD+ capped transcriptome of Arabidopsis thaliana2666-166710.1016/j.xpro.2021.100901https://doaj.org/article/e3b2951872f144749e381e62ce4ac6862021-12-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2666166721006079https://doaj.org/toc/2666-1667Summary: Eukaryotic RNAs can be modified with a non-canonical 5′ nicotinamide adenine dinucleotide (NAD+) cap. NAD-seq identifies transcriptome-wide NAD+ capped RNAs. NAD-seq takes advantage of click chemistry to allow the capture of NAD+ capped RNAs. Unlike other approaches, NAD-seq does not require DNA synthesis on beads, but this technique uses full NAD+ capped transcripts eluted from beads as the substrates for strand-specific RNA sequencing library preparation.For complete details on the use and execution of this protocol, please refer to Yu et al. (2021).Xiang YuLee E. VandivierBrian D. GregoryElsevierarticleGenomicsRNAseqModel OrganismsPlant sciencesMolecular BiologyGene ExpressionScience (General)Q1-390ENSTAR Protocols, Vol 2, Iss 4, Pp 100901- (2021) |
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DOAJ |
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Genomics RNAseq Model Organisms Plant sciences Molecular Biology Gene Expression Science (General) Q1-390 |
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Genomics RNAseq Model Organisms Plant sciences Molecular Biology Gene Expression Science (General) Q1-390 Xiang Yu Lee E. Vandivier Brian D. Gregory NAD-seq for profiling the NAD+ capped transcriptome of Arabidopsis thaliana |
description |
Summary: Eukaryotic RNAs can be modified with a non-canonical 5′ nicotinamide adenine dinucleotide (NAD+) cap. NAD-seq identifies transcriptome-wide NAD+ capped RNAs. NAD-seq takes advantage of click chemistry to allow the capture of NAD+ capped RNAs. Unlike other approaches, NAD-seq does not require DNA synthesis on beads, but this technique uses full NAD+ capped transcripts eluted from beads as the substrates for strand-specific RNA sequencing library preparation.For complete details on the use and execution of this protocol, please refer to Yu et al. (2021). |
format |
article |
author |
Xiang Yu Lee E. Vandivier Brian D. Gregory |
author_facet |
Xiang Yu Lee E. Vandivier Brian D. Gregory |
author_sort |
Xiang Yu |
title |
NAD-seq for profiling the NAD+ capped transcriptome of Arabidopsis thaliana |
title_short |
NAD-seq for profiling the NAD+ capped transcriptome of Arabidopsis thaliana |
title_full |
NAD-seq for profiling the NAD+ capped transcriptome of Arabidopsis thaliana |
title_fullStr |
NAD-seq for profiling the NAD+ capped transcriptome of Arabidopsis thaliana |
title_full_unstemmed |
NAD-seq for profiling the NAD+ capped transcriptome of Arabidopsis thaliana |
title_sort |
nad-seq for profiling the nad+ capped transcriptome of arabidopsis thaliana |
publisher |
Elsevier |
publishDate |
2021 |
url |
https://doaj.org/article/e3b2951872f144749e381e62ce4ac686 |
work_keys_str_mv |
AT xiangyu nadseqforprofilingthenadcappedtranscriptomeofarabidopsisthaliana AT leeevandivier nadseqforprofilingthenadcappedtranscriptomeofarabidopsisthaliana AT briandgregory nadseqforprofilingthenadcappedtranscriptomeofarabidopsisthaliana |
_version_ |
1718429929750659072 |