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Development of the light-harvesting chlorophyll antenna in the green alga Chlamydomonas reinhardtii is regulated by the novel Tla1 gene

机译:新型藻类Tla1基因调控绿藻衣藻衣藻捕光叶绿素触角的发育

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The Chlamydomonas reinhardtii tla1 (truncated light-harvesting chlorophyll antenna size) mutant was generated upon DNA insertional mutagenesis and shown to specifically possess a smaller than wild type (WT) chlorophyll antenna size in both photosystems. Molecular and genetic analysis revealed that the exogenous plasmid DNA was inserted at the end of the 5′ UTR and just prior to the ATG start codon of a hitherto unknown nuclear gene (termed Tla1), which encodes a protein of 213 amino acids. The Tla1 gene in the mutant is transcribed with a new 5′ UTR sequence, derived from the 3′ end of the transforming plasmid. This replacement of the native 5′ UTR and promoter regions resulted in enhanced transcription of the tla1 gene in the mutant but inhibition in the translation of the respective tla1 mRNA. Transformation of the tla1 mutant with WT Tla1 genomic DNA successfully rescued the mutant. These results are evidence that polymorphism in the 5′ UTR of the Tla1 transcripts resulted in the tla1 phenotype and that expression of the Tla1 gene is a prerequisite for the development/assembly of the Chl antenna in C. reinhardtii. A blast search with the Tla1 deduced amino acid sequence revealed that this protein is highly conserved in many eukaryotes. It showed homology to a protein of unknown function in Arabidopsis thaliana (73%), Oryza sativa (76%), Drosophila melanogaster (71%) and Homo sapiens (67%). The Tla1 gene apparently regulates genes that define the Chl antenna size in the photosynthetic apparatus of C. reinhardtii. Potential applications of the Tla1 gene in photosynthesis and biotechnology are discussed.
机译:DNA插入诱变后产生了衣藻衣藻tla1(截短的集光叶绿素天线大小)突变体,并且在两个光系统中都显示出比野生型(WT)叶绿素天线大小特别小。分子和遗传分析表明,外源质粒DNA插入了一个迄今未知的核基因(称为Tla1)的ATG起始密码子的5'UTR末端,该基因编码213个氨基酸。突变体中的Tla1基因转录有新的5'UTR序列,该序列来自转化质粒的3'末端。天然5'UTR和启动子区域的这种替换导致突变体中tla1基因的转录增强,但抑制了相应tla1 mRNA的翻译。用WT Tla1基因组DNA转化tla1突变体成功拯救了该突变体。这些结果证明了Tla1转录本的5'UTR中的多态性导致tla1表型,并且Tla1基因的表达是在莱茵衣藻中开发/装配Chl天线的前提。用Tla1推导的氨基酸序列进行blast搜索表明,该蛋白在许多真核生物中高度保守。它与拟南芥(73%),水稻(76%),果蝇(71%)和智人(67%)中功能未知的蛋白质显示出同源性。 Tla1基因显然调节在莱茵衣藻光合作用中定义Chl天线大小的基因。讨论了Tla1基因在光合作用和生物技术中的潜在应用。

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