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Multiple features contribute to efficient constitutive splicing of anunusually large exon

机译:多重特征有助于异常大外显子的有效本构拼接

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Vertebrate internal exons are usually between 50 and 400 nt long; exons outside this size range may require additional exonic and/or intronic sequences to be spliced into the mature mRNA, The mouse polymeric immunoglobulin receptor gene has a 654 nt exon that is efficiently spliced into the mRNA, We have examined this exon to identify features that contribute to its efficient splicing despite its large size; a large constitutive exon has not been studied previously. We found that a strong 5' splice site is necessary for this exon to be spliced intact, but the splice sites alone were not sufficient to efficiently splice a large exon, At least two exonic sequences and one evolutionarily conserved intronic sequence also contribute to recognition of this exon, However, these elements have redundant activities as they could only be detected in conjunction with other mutations that reduced splicing efficiency, Several mutations activated cryptic 5' splice sites that created smaller exons, Thus, the balance between use of these potential sites and the authentic 5' splice site must be modulated by sequences that repress or enhance use of these sites, respectively. Also, sequences that enhance cryptic splice site use must be absent from this large exon.
机译:脊椎动物内部外显子的长度通常在50至400 nt之间。超出此大小范围的外显子可能需要将其他外显子和/或内含子序列剪接到成熟的mRNA中。小鼠聚合免疫球蛋白受体基因具有一个654 nt的外显子,可以有效地剪接到该mRNA中。尽管尺寸很大,但仍有助于其高效拼接;先前尚未研究过大的本构外显子。我们发现强大的5'剪接位点是完整剪接此外显子所必需的,但是仅剪接位点不足以有效剪接大外显子,至少两个外显子序列和一个进化保守的内含子序列也有助于识别但是,这些元件具有多余的活性,因为它们只能与其他降低剪接效率的突变结合在一起才能检测到。一些突变激活了产生较小外显子的隐蔽5'剪接位点,因此,这些潜在位点和真实的5'剪接位点必须分别通过抑制或增强这些位点的序列进行调控。而且,该大外显子必须缺少增强隐蔽剪接位点使用的序列。

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