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对两个玉米(L.)品种中响应化学肥料和生物肥料而调控的丝氨酸/苏氨酸蛋白激酶编码基因的生物信息学和实证分析。

Bioinformatic and empirical analysis of a gene encoding serine/threonine protein kinase regulated in response to chemical and biological fertilizers in two maize ( L.) cultivars.

作者信息

Azad Ida, Alemzadeh Abbas

机构信息

Department of Crop Production and Plant Breeding, School of Agriculture, Shiraz University, Shiraz, Iran.

Plant Breeding and Biotechnology Department, Agricultural Sciences and Natural Resources University of Sari, Sari, Iran.

出版信息

Mol Biol Res Commun. 2017 Jun;6(2):65-75.

Abstract

Molecular structure of a gene, , encoding a serine/threonine protein kinase in maize was analyzed by bioinformatic tool and its expression pattern was studied under chemical biological fertilizers. Bioinformatic analysis cleared that is located on chromosome 10, from position 141015332 to 141017582. The full genomic sequence of the gene is 2251 bp in length and includes 2 exons. Its cDNA length is 1900 bp with a 5'-untranslated region of 311 bp and 3'-untranslated region of 341 bp, of which 1248 bp from open reading frame encoding 415 amino acid residues with a molecular weight of 46 kDa and an isoelectric point 7.2. Also, an upstream open reading frame contains 100 aa was found at -12 position from ATG initiation codon. ZmSTPK1 with a long half-life, 10 hours in , and instability index of 32.25 is classified as a stable protein. A calmodulin binding domain was found in ZmSTPK1 at position from 395 to 405 in C-terminal end. The helical wheel analysis showed that the stretch of residues Ile-395 to Asp-415 has the potential to form a charged amphiphilic -helix characteristic of a calmodulin-binding region. Two -like motifs, which are present in the promoter regions of Pi starvation-induced genes, were located at positions -48 and -867 from ATG initiation codon. The expression of responded to available phosphate, and its expression up-regulated under phosphate starvation.

摘要

利用生物信息学工具分析了玉米中一个编码丝氨酸/苏氨酸蛋白激酶的基因的分子结构,并研究了其在化学生物肥料作用下的表达模式。生物信息学分析表明,该基因位于第10号染色体上,位置为141015332至141017582。该基因的全基因组序列长度为2251 bp,包含2个外显子。其cDNA长度为1900 bp,5'非翻译区为311 bp,3'非翻译区为341 bp,其中1248 bp来自开放阅读框,编码415个氨基酸残基,分子量为46 kDa,等电点为7.2。此外,在距ATG起始密码子-12位处发现一个上游开放阅读框,包含100个氨基酸。ZmSTPK1半衰期较长,在[具体条件]下为10小时,不稳定指数为32.25,被归类为稳定蛋白。在ZmSTPK1的C末端395至405位发现一个钙调蛋白结合结构域。螺旋轮分析表明,从Ile-395到Asp-415的残基 stretch 有可能形成钙调蛋白结合区域特有的带电荷两亲性α-螺旋。在距ATG起始密码子-48和-867位发现了两个类似于Pi饥饿诱导基因启动子区域中的基序。该基因的表达对有效磷有响应,在磷饥饿条件下其表达上调。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1515/5534521/44b25f8afc78/mbrc-6-065-g001.jpg

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