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Multiple tandem splicing silencer elements suppress aberrant splicing within the long exon 26 of the human Apolipoprotein B gene

机译:多个串联剪接沉默元件抑制人类载脂蛋白B基因长外显子26内的异常剪接

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摘要

Apolipoprotein B (APOB) is an integral component of the chylomicron and the atherogenic lipoproteins LDL and Lp(a). Exon 26 of the APOB pre-mRNA is unusually long at 7,572 nt and is constitutively spliced. It is also subject to RNA editing in the intestine, which generates a shortened isoform, APOB48, assembled exclusively into chylomicrons. Due to its length, exon 26 contains multiple pseudo splice sites which are not spliced, but which conform to the degenerate splice site consensus. We demonstrate that these pseudo splice sites are repressed by multiple, tandem splicing silencers distributed along the length of exon 26. The distribution of these elements appears to be heterogeneous, with a greater frequency in the middle 4,800 nt of the exon. Repression of these splice sites is key to maintaining the integrity of exon 26 during RNA splicing and therefore the correct expression of both isoforms of APOB.
机译:载脂蛋白B(APOB)是乳糜微粒和致动脉粥样硬化脂蛋白LDL和Lp(a)的组成部分。 APOB前mRNA的第26外显子异常长,长度为7,572 nt,并进行了结构性剪接。它还需要在肠道中进行RNA编辑,从而生成短的同种型APOB48,仅组装成乳糜微粒。由于其长度,外显子26包含多个未剪接但符合简并剪接位点共有的假剪接位点。我们证明,这些伪剪接位点受到沿着外显子26长度分布的多个串联剪接沉默子的抑制。这些元素的分布似乎是异质的,在外显子的中间4,800 nt处出现频率更高。抑制这些剪接位点是在RNA剪接过程中维持外显子26完整性以及因此正确表达APOB的两种同工型的关键。

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