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首页> 外文期刊>Journal of crop science and Biotechnology >In Silico Identification of Cis-Regulatory Elements of Phosphate Transporter Genes in Rice (Oryza sativa L.)
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In Silico Identification of Cis-Regulatory Elements of Phosphate Transporter Genes in Rice (Oryza sativa L.)

机译:在水稻中磷酸盐转运基因的顺式调节元素的硅鉴定(Oryza Sativa L.)

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摘要

Promoter sequences of 13 Phosphate Transporter genes of Oryza sativa L. (OsPTs) have been analyzed in silico to identify their eft-regulatory elements (CREs). The DNA sequences of these OsPT genes were mined from NCBI gene databases. MEGABLAST programwas used to align these sequences to Rice Genome Database in obtaining their complete sequences. The upstream region (-1 to -400) of the complete gene sequences were analyzed using SIGNALSCAN program provided by PLACE database of ds-regulato-ry elementmotives. From this procedure, 153 types of CRE were identified. Four of these CREs were found on all of the OsPT genes: ARR1AT, CAATBOX1, CACTFTPPCA1, and DOFCOREZM. Among these CREs, CACTFTPPCA1 was found with 3 to 15 duplications in each cw-regulatorysequence. In addition, each OsPT gene has typical CREs that can only be found in the respective genes. The total number of these typical CREs is 54, and one of them was a binding site for a bHLH-like protein, CACGTGMOTIF or the G-box. Moreover, several E-boxes which also functioned as a binding site for a bHLH-like protein were identified in all OsPTs except in OsPTl, OsPT6, and OsPT8. There were significant correlations (p < 0.05) between mRNA levels of OsPTl to OsPT 11 in rice root with or without inoculation of Glomus intradices reported by Paszkowskidagger et al. (2002) and the duplication numbers of ARR1AT, CAATBOX1, CACTFTPPCA1, CURECORECR, and WRKY710S.
机译:在硅藻中分析了13例磷酸盐转运蛋白基因的促进剂序列,以鉴定其EFT调节元素(CRE)。这些OSPT基因的DNA序列由NCBI基因数据库开采。 Megablast程序用于将这些序列对准到赖斯基因组数据库中获取完整序列。使用DS-Squarato-Ry元素元素的位置数据库提供的信号CAN程序分析完整基因序列的上游区域(-1至-400)。从该过程中,确定了153种CRE。在所有OSPT基因中发现了四个杂志:ARR1AT,CAATBOX1,CACTFTPPCA1和DOFCOREZM。在这些CRE中,在每个CW-incumetationsequency中发现CactftpPCA1 3至15个重复。此外,每个OSPT基因具有典型的CRE,其只能在各自的基因中发现。这些典型的CRE的总数为54,其中一个是BHLH样蛋白,CACGTGMOTIF或G箱的结合位点。此外,除了OSPT1,OSPT6和OSPT8之外,在所有OSPT中鉴定出几种作为BHLH样蛋白的结合位点的若干e盒。在稻草中的OSPT1至OSPT11的MRNA水平之间存在显着的相关性(P <0.05),或者没有接种Paszkowskidger等人报告的Glomus内部。 (2002)和ARR1AT,CAATBOX1,CACTFTPPCA1,CURECORECR和WRKY710S的重复编号。

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