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LIN28假基因家族的DNA甲基化

DNA methylation of the LIN28 pseudogene family.

作者信息

Davis Aaron P, Benninghoff Abby D, Thomas Aaron J, Sessions Benjamin R, White Kenneth L

机构信息

Department of Animal, Dairy and Veterinary Sciences, Utah State University, 4815 Old Main Hill, Logan, UT, 84322-4815, USA.

School of Veterinary Medicine, Utah State University, Logan, UT, USA.

出版信息

BMC Genomics. 2015 Apr 11;16(1):287. doi: 10.1186/s12864-015-1487-3.

Abstract

BACKGROUND

DNA methylation directs the epigenetic silencing of selected regions of DNA, including the regulation of pseudogenes, and is widespread throughout the genome. Pseudogenes are decayed copies of duplicated genes that have spread throughout the genome by transposition. Pseudogenes are transcriptionally silenced by DNA methylation, but little is known about how pseudogenes are targeted for methylation or how methylation levels are maintained in different tissues.

RESULTS

We employed bisulfite next generation sequencing to examine the methylation status of the LIN28 gene and four processed pseudogenes derived from LIN28. The objective was to determine whether LIN28 pseudogenes maintain the same pattern of methylation as the parental gene or acquire a methylation pattern independent of the gene of origin. In this study, we determined that the methylation status of LIN28 pseudogenes does not resemble the pattern evident for the LIN28 gene, but rather these pseudogenes appear to acquire methylation patterns independent of the parental gene. Furthermore, we observed that methylation levels of the examined pseudogenes correlate to the location of insertion within the genome. LIN28 pseudogenes inserted into gene bodies were highly methylated in all tissues examined. In contrast, pseudogenes inserted into genomic regions that are not proximal to genes were differentially methylated in various tissue types.

CONCLUSIONS

Our analysis suggests that Lin28 pseudogenes do not acquire patterns of tissue-specific methylation as for the parental gene, but rather are methylated in patterns specific to the local genomic environment into which they were inserted.

摘要

背景

DNA甲基化指导DNA特定区域的表观遗传沉默,包括假基因的调控,且在整个基因组中广泛存在。假基因是通过转座在基因组中扩散的重复基因的衰变拷贝。假基因通过DNA甲基化转录沉默,但对于假基因如何被靶向甲基化或甲基化水平如何在不同组织中维持知之甚少。

结果

我们采用亚硫酸氢盐下一代测序来检测LIN28基因以及源自LIN28的四个加工假基因的甲基化状态。目的是确定LIN28假基因是否维持与亲本基因相同的甲基化模式,或者是否获得独立于起源基因的甲基化模式。在本研究中,我们确定LIN28假基因的甲基化状态与LIN28基因明显的模式不同,而是这些假基因似乎获得了独立于亲本基因的甲基化模式。此外,我们观察到所检测假基因的甲基化水平与基因组内的插入位置相关。插入基因体内的LIN28假基因在所有检测组织中高度甲基化。相比之下,插入到与基因不相邻的基因组区域的假基因在各种组织类型中甲基化存在差异。

结论

我们的分析表明,Lin28假基因不像亲本基因那样获得组织特异性甲基化模式,而是以其插入的局部基因组环境特有的模式被甲基化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a230/4404226/1c51e848dc55/12864_2015_1487_Fig1_HTML.jpg

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