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Retroviral sequences located within an intron of the dilute gene alter dilute expression in a tissue-specific manner.

机译:位于稀释基因内含子内的逆转录病毒序列以组织特异性方式改变稀释表达。

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摘要

The murine dilute coat color locus encodes an unconventional myosin heavy chain that is thought to be required for the elaboration or maintenance of dendrites or organelle transport in melanocytes and neurons. In previous studies we showed that the d mutation carried by many inbred strains of mice (now referred to as dilute viral, dv), is caused by the integration of an ecotropic murine leukemia virus (Emv-3) into the dilute gene and that phenotypic revertants of dv (termed d+) result from viral excision; a solo viral long terminal repeat (LTR) is all that remains in revertant DNA. In the studies described here we show that Emv-3 sequences are located within an intron of the dilute gene in a region of the C-terminal tail that is differentially spliced. We also show that these Emv-3 sequences result in the production of shortened and abnormally spliced dilute transcripts and that the level of this effect varies among tissues. This tissue-specific effect on dilute expression likely accounts for the absence of neurological abnormalities observed in dv mice. Surprisingly, we also found that the solo viral LTR present in revertant d+ DNA produces a tissue-specific effect on dilute expression, although this effect is less dramatic than with the full-length provirus and produces no obvious mutant phenotype. These findings have important implications for understanding the effects of viral sequences on mammalian gene expression.
机译:鼠的稀薄外套色基因座编码一条非常规的肌球蛋白重链,据认为对于黑素细胞和神经元中树突的形成或维持或细胞器的运输是必需的。在以前的研究中,我们证明了许多近交系小鼠携带的d突变(现在称为稀病毒dv),是由向嗜性小鼠白血病病毒(Emv-3)整合到稀有基因中并造成了表型dv的回复子(称为d +)是由于病毒切除而产生的;病毒DNA的长末端重复序列(LTR)就是全部。在此处描述的研究中,我们显示Emv-3序列位于差异剪接的C末端尾部区域中的稀释基因的内含子内。我们还表明,这些Emv-3序列导致缩短和异常剪接的稀释转录物的产生,并且这种效应的水平在组织之间有所不同。这种对稀疏表达的组织特异性作用可能是在dv小鼠中观察不到神经异常的原因。出人意料的是,我们还发现存在于回复性d + DNA中的病毒LTR对稀释表达产生组织特异性作用,尽管这种作用不如全长原病毒显着,并且不产生明显的突变表型。这些发现对于理解病毒序列对哺乳动物基因表达的影响具有重要意义。

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