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首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Lineage specific evolutionary events on SFTPB gene: Alu recombination-mediated deletion (ARMD), exonization, and alternative splicing events.
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Lineage specific evolutionary events on SFTPB gene: Alu recombination-mediated deletion (ARMD), exonization, and alternative splicing events.

机译:SFTPB基因的谱系特异性进化事件:ALU重组介导的缺失(ARMD),出口和替代剪接事件。

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摘要

SFTPB gene encoding pulmonary surfactant protein has been investigated to have transcript variants related with transposable elements (TEs). To investigate the alternative splicing event on SFTPB gene, various primate samples (tissue RNA and genomic DNA) were used. Two different transcript variants (T1-2 and T2-2) were newly identified by RT-PCR analysis. T1-1,-2 and T2-1,-2 are TE-related and original transcripts, respectively. T1-1 transcript was investigated to be a lung and human specific alternative transcript. T2-1 transcript shows dominant expression pattern in lung tissues. T1-related TEs (LTR7B and AluSx) were investigated by genomic PCR and sequencing procedure of different primate genomic DNAs. Sequencing analysis indicated that they had been integrated into our common ancestor genome before the divergence of simian and prosimian and Alu recombination-mediated deletion (ARMD) event had been occurred on our common ancestor genome after the divergence of New World monkeys and Old World monkeys in SFTPB gene 3' UTR region. Taken together, integration event of LTR7B and AluSx on SFTPB gene seem to cause lineage specific events via general exonization event (New World monkeys and prosimian), ARMD event (Old World monkeys and hominoids), and alternative splicing (human) during the primate evolution.
机译:已经研究了编码肺表面活性剂蛋白的SFTPB基因,具有与可转换元件(TES)相关的转录变体。为了研究SFTPB基因上的替代剪接事件,使用各种灵长类脉(组织RNA和基因组DNA)。通过RT-PCR分析新鉴定出两种不同的转录变体(T1-2和T2-2)。 T1-1,-2和T2-1,-2分别为TE相关和原始转录物。研究了T1-1转录物是肺和人的特异性替代转录物。 T2-1转录物在肺组织中显示出显性表达模式。通过基因组PCR和不同灵长类会基因组DNA的测序程序研究了T1相关的TES(LTR7B和ALUSX)。测序分析表明,在新世界猴子和老世界猴子的分歧之后,他们已经纳入了猿猴和潜水和尿尿的疾病和Alu重组介导的删除(ARMAD)事件之前纳入了我们共同的祖先基因组。 SFTPB基因3'UTR区域。在一起,LTR7B和Alusx的集成事件在SFTPB基因上似乎通过通用出口事件(新世界猴子和Prosimian),ARMAD活动(旧世界猴子和Hominoids),以及在灵长类动物演变期间的替代拼接(人类)造成血统特定事件。

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