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Prediction of bipartite transcriptional regulatory elements using transcriptome data of Arabidopsis.


ABSTRACT: In our previous study, a methodology was established to predict transcriptional regulatory elements in promoter sequences using transcriptome data based on a frequency comparison of octamers. Some transcription factors, including the NAC family, cannot be covered by this method because their binding sequences have non-specific spacers in the middle of the two binding sites. In order to remove this blind spot in promoter prediction, we have extended our analysis by including bipartite octamers that are composed of '4 bases-a spacer with a flexible length-4 bases'. 8,044 pre-selected bipartite octamers, which had an overrepresentation of specific spacer lengths in promoter sequences and sequences related to core elements removed, were subjected to frequency comparison analysis. Prediction of ER stress-responsive elements in the BiP/BiPL promoter and an ANAC017 target sequence resulted in precise detection of true positives, judged by functional analyses of a reported article and our own in vitro protein-DNA binding assays. These results demonstrate that incorporation of bipartite octamers with continuous ones improves promoter prediction significantly.

SUBMITTER: Yamamoto YY 

PROVIDER: S-EPMC5499772 | biostudies-literature | 2017 Jun

REPOSITORIES: biostudies-literature

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Prediction of bipartite transcriptional regulatory elements using transcriptome data of Arabidopsis.

Yamamoto Yoshiharu Y YY   Ichida Hiroyuki H   Hieno Ayaka A   Obata Daichi D   Tokizawa Mutsutomo M   Nomoto Mika M   Tada Yasuomi Y   Kusunoki Kazutaka K   Koyama Hiroyuki H   Hayami Natsuki N  

DNA research : an international journal for rapid publication of reports on genes and genomes 20170601 3


In our previous study, a methodology was established to predict transcriptional regulatory elements in promoter sequences using transcriptome data based on a frequency comparison of octamers. Some transcription factors, including the NAC family, cannot be covered by this method because their binding sequences have non-specific spacers in the middle of the two binding sites. In order to remove this blind spot in promoter prediction, we have extended our analysis by including bipartite octamers th  ...[more]

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