z-logo
open-access-imgOpen Access
Analysis of cis-regulatory element distribution in gene promoters of Gossypium raimondii and Arabidopsis thaliana
Author(s) -
Gaofei Sun,
Shoupu He,
Xiongming Du
Publication year - 2013
Publication title -
yichuan
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.125
H-Index - 16
ISSN - 0253-9772
DOI - 10.3724/sp.j.1005.2013.01226
Subject(s) - biology , genome , gene , promoter , genetics , arabidopsis , gossypium , untranslated region , arabidopsis thaliana , transcription (linguistics) , regulatory sequence , transcription factor , rna , gene expression , mutant , linguistics , philosophy
Cotton genomic studies have boomed since the release of Gossypium raimondii draft genome. In this study, cis-regulatory element (CRE) in 1 kb length sequence upstream 5' UTR of annotated genes were selected and scanned in the Arabidopsis thaliana (At) and Gossypium raimondii (Gr) genomes, based on the database of PLACE (Plant cis-acting Regulatory DNA Elements). According to the definition of this study, 44 (12.3%) and 57 (15.5%) CREs presented "peak-like" distribution in the 1 kb selected sequences of both genomes, respectively. Thirty-four of them were peak-like distributed in both genomes, which could be further categorized into 4 types based on their core sequences. The coincidence of TATABOX peak position and their actual position ((-) -30 bp) indicated that the position of a common CRE was conservative in different genes, which suggested that the peak position of these CREs was their possible actual position of transcription factors. The position of a common CRE was also different between the two genomes due to stronger length variation of 5' UTR in Gr than At. Furthermore, most of the peak-like CREs were located in the region of -110 bp-0 bp, which suggested that concentrated distribution might be conductive to the interaction of transcription factors, and then regulate the gene expression in downstream.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here