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首页> 外文期刊>Plant Molecular Biology >The gene encoding T protein of the glycine decarboxylase complex involved in the mitochondrial step of the photorespiratory pathway in plants exhibits features of light-induced genes
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The gene encoding T protein of the glycine decarboxylase complex involved in the mitochondrial step of the photorespiratory pathway in plants exhibits features of light-induced genes

机译:参与植物光呼吸途径线粒体步骤的甘氨酸脱羧酶复合物T蛋白编码基因表现出光诱导基因的特征

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A genomic clone encoding the 41 kDa monomer T-protein was isolated from pea (Pisum sativum cv. Alaska) and characterized. This gene, called gdcT, spans approximately 3 kb and is composed of four exons interrupted by three introns (of 321, 691 and 114 bp). The splice sites for donor and acceptor are in agreement with the canonical GT/AG rule. Primer extension strongly suggests the presence of two major transcription start sites. The first transcription start site, around 43 bases downstream of a putative TATA box, was assigned the +1 position. The second (+31) is not correlated with a putative TATA box, but revealed a pyrimidine-rich region which similar to the initiator element. Sequence analysis of the 5'-upstream region of the gene revealed three consensus regions found in the nuclear genes encoding the chloroplastic proteins of ribulose-bisphosphate carboxylase (rbcS) and the chlorophyll a/b-binding protein (cab), such as an AT-rich sequence localized at -539 to -530, a box II core sequence GGTTAA (-123 to -118) and, between -364 and -354, a tandem GATA motif. These elements are known to be involved in the regulation of light-responsiveness and cell-type specificity expression of plant genes. Gel shift assays indicated that the box II core sequence could bind protein nuclear factors similar to the trans-acting factor which interacts with the corresponding promoter region of rbcS gene. Nucleotide sequence data have been submitted to the EMBL/GenBank/DDBJ databases under the accession number AJ222771.
机译:从豌豆(Pisum sativum cv。Alaska)中分离出编码41 kDa单体T蛋白的基因组克隆并进行了鉴定。该基因称为gdcT,跨度约为3 kb,由四个外显子组成,这些外显子被三个内含子(321、691和114 bp)打断。供体和受体的剪接位点符合规范的GT / AG规则。引物延伸强烈提示存在两个主要的转录起始位点。在假定的TATA盒下游43个碱基附近的第一个转录起始位点被指定为+1位。第二个(+31)与推定的TATA框不相关,但是显示了一个富含嘧啶的区域,该区域类似于引发剂元素。基因5'上游区域的序列分析显示,在编码核糖双磷酸羧化酶(r​​bcS)和叶绿素a / b结合蛋白(cab)的叶绿体蛋白的核基因中发现了三个共有区域,例如AT -富集的序列位于-539至-530,是框II的核心序列GGTTAA(-123至-118),以及在-364至-354之间的串联GATA基序。已知这些元素参与植物基因的光响应性和细胞类型特异性表达的调节。凝胶位移分析表明,box II核心序列可以结合类似于反式作用因子的蛋白质核因子,而反式作用因子与rbcS基因的相应启动子区域相互作用。核苷酸序列数据已以登录号AJ222771提交至EMBL / GenBank / DDBJ数据库。

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