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小鼠的常染色体单等位基因表达。

Autosomal monoallelic expression in the mouse.

机构信息

Center for Human Genetic Research, Massachusetts General Hospital, Boston, MA 02114, USA.

出版信息

Genome Biol. 2012 Feb 20;13(2):R10. doi: 10.1186/gb-2012-13-2-r10.

Abstract

BACKGROUND

Random monoallelic expression defines an unusual class of genes displaying random choice for expression between the maternal and paternal alleles. Once established, the allele-specific expression pattern is stably maintained and mitotically inherited. Examples of random monoallelic genes include those found on the X-chromosome and a subset of autosomal genes, which have been most extensively studied in humans. Here, we report a genome-wide analysis of random monoallelic expression in the mouse. We used high density mouse genome polymorphism mapping arrays to assess allele-specific expression in clonal cell lines derived from heterozygous mouse strains.

RESULTS

Over 1,300 autosomal genes were assessed for allele-specific expression, and greater than 10% of them showed random monoallelic expression. When comparing mouse and human, the number of autosomal orthologs demonstrating random monoallelic expression in both organisms was greater than would be expected by chance. Random monoallelic expression on the mouse autosomes is broadly similar to that in human cells: it is widespread throughout the genome, lacks chromosome-wide coordination, and varies between cell types. However, for some mouse genes, there appears to be skewing, in some ways resembling skewed X-inactivation, wherein one allele is more frequently active.

CONCLUSIONS

These data suggest that autosomal random monoallelic expression was present at least as far back as the last common ancestor of rodents and primates. Random monoallelic expression can lead to phenotypic variation beyond the phenotypic variation dictated by genotypic variation. Thus, it is important to take into account random monoallelic expression when examining genotype-phenotype correlation.

摘要

背景

随机单等位基因表达定义了一类不寻常的基因,它们在母源和父源等位基因之间表现出随机选择表达。一旦建立,等位基因特异性表达模式就会稳定维持并通过有丝分裂遗传。随机单等位基因基因的例子包括 X 染色体上的基因和一部分常染色体基因,这些基因在人类中得到了最广泛的研究。在这里,我们报告了在小鼠中进行的全基因组随机单等位基因表达分析。我们使用高密度小鼠基因组多态性映射阵列来评估来自杂合小鼠品系的克隆细胞系中的等位基因特异性表达。

结果

超过 1300 个常染色体基因被评估为等位基因特异性表达,其中超过 10%表现出随机单等位基因表达。当比较小鼠和人类时,在这两种生物体中表现出随机单等位基因表达的常染色体同源基因数量超过了随机预期。小鼠常染色体上的随机单等位基因表达与人类细胞中的表达大致相似:它广泛分布于整个基因组,缺乏染色体级别的协调,并且在细胞类型之间存在差异。然而,对于一些小鼠基因,似乎存在偏倚,在某些方面类似于偏倚的 X 染色体失活,其中一个等位基因更频繁地活跃。

结论

这些数据表明,至少在啮齿动物和灵长类动物的最后共同祖先时期,常染色体上就存在随机单等位基因表达。随机单等位基因表达可以导致除由基因型变异决定的表型变异之外的表型变异。因此,在检查基因型-表型相关性时,考虑随机单等位基因表达是很重要的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be63/3334567/3c8210b506ab/gb-2012-13-2-r10-1.jpg

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