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Sequence and transcription analysis of the Petunia mitochondrial gene for the ATP synthase proteolipid subunil

机译:矮牵牛线粒体ATP合酶蛋白脂亚基的基因序列和转录分析

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We have sequenoed the Petunia hybrida gene that specifies the proteolipid subunit of the mitochondrial Fo ATP synthase and have used this gene to investigate plant mitochondrial gene transcription. The Petunia atp 9 gene contains a single open-reading frame capable of specifying a 77 amino acid-polypeptide that is homologous to bovine, fungal and maize proteolipid subunits. S1 protection identified 3 transcripts in a ratio of 1: 5: 100 in the Petunia tissues tested. The transcripts share a common 3′ terminus but have 5′ termini that map 528, 266, and 121 nucleotides upstream of the translation start site. The 5′ terminus of the longest transcript maps to the sequence ATATAGTA, which is nearly identical to the yeast mitochondrial transcription initiation site ATATAAGTA. Primer extension analysis indicates that these two shorter transcripts are not due to splicing. The two shorter transcripts originate at sequences homologous to sites at 5′ termini of two pea and maize genes. These consensus sequences may signal processing events other than splicing.
机译:我们已经隔离了矮牵牛杂交基因,该基因指定了线粒体F o ATP合酶的蛋白脂亚基,并已使用该基因研究植物线粒体基因的转录。矮牵牛atp 9基因包含一个单一的开放阅读框,该框能够指定与牛,真菌和玉米蛋白脂质亚基同源的77个氨基酸的多肽。 S1保护在测试的矮牵牛组织中鉴定出3个转录本,比例为1:5:100。转录本共享一个公共的3'末端,但具有5'末端,该末端将528、266和121个核苷酸映射到翻译起始位点的上游。最长的转录物的5'末端映射到序列ATATAGTA,该序列与酵母线粒体转录起始位点ATATAAGTA几乎相同。引物延伸分析表明这两个较短的转录本不是由于剪接引起的。这两个较短的转录物起源于与两个豌豆和玉米基因的5'末端的位点同源的序列。这些共有序列可能表示除拼接以外的处理事件。

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