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Z-DNA 结合的人类内源性逆转录病毒家族的长末端重复序列为人类功能基因提供了替代启动子。

Z-DNA-Containing Long Terminal Repeats of Human Endogenous Retrovirus Families Provide Alternative Promoters for Human Functional Genes.

机构信息

Department of Integrated Biological Sciences, Pusan National University, Busan 46241, Korea.

Institute of Systems Biology, Pusan National University, Busan 46241, Korea.

出版信息

Mol Cells. 2022 Aug 31;45(8):522-530. doi: 10.14348/molcells.2022.0060. Epub 2022 Aug 5.

DOI:10.14348/molcells.2022.0060
PMID:35950452
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9385571/
Abstract

Transposable elements (TEs) account for approximately 45% of the human genome. TEs have proliferated randomly and integrated into functional genes during hominoid radiation. They appear as right-handed B-DNA double helices and slightly elongated left-handed Z-DNAs. Human endogenous retrovirus (HERV) families are widely distributed in human chromosomes at a ratio of 8%. They contain a 5'-long terminal repeat (LTR)-gag-pol-env-3'-LTR structure. LTRs contain the U3 enhancer and promoter region, transcribed R region, and U5 region. LTRs can influence host gene expression by acting as regulatory elements. In this review, we describe the alternative promoters derived from LTR elements that overlap Z-DNA by comparing Z-hunt and DeepZ data for human functional genes. We also present evidence showing the regulatory activity of LTR elements containing Z-DNA in . Taken together, the regulatory activity of LTR elements with Z-DNA allows us to understand gene function in relation to various human diseases.

摘要

转座元件 (TEs) 约占人类基因组的 45%。TEs 在人科辐射过程中随机增殖并整合到功能基因中。它们呈现右手 B-DNA 双螺旋结构和略微拉长的左手 Z-DNA。人类内源性逆转录病毒 (HERV) 家族广泛分布于人类染色体上,比例为 8%。它们包含 5'-长末端重复 (LTR)-gag-pol-env-3'-LTR 结构。LTR 包含 U3 增强子和启动子区域、转录 R 区域和 U5 区域。LTR 可以通过作为调节元件来影响宿主基因表达。在这篇综述中,我们通过比较 Z-hunt 和 DeepZ 数据来描述来自 LTR 元件的替代启动子,这些启动子与 Z-DNA 重叠。我们还提供了含有 Z-DNA 的 LTR 元件具有调节活性的证据。综上所述,含有 Z-DNA 的 LTR 元件的调节活性使我们能够了解与各种人类疾病相关的基因功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13f2/9385571/851591416c59/molce-45-8-522-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13f2/9385571/e26cb31b03c7/molce-45-8-522-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13f2/9385571/5a457c4e0cc4/molce-45-8-522-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13f2/9385571/c716b40cd03b/molce-45-8-522-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13f2/9385571/851591416c59/molce-45-8-522-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13f2/9385571/e26cb31b03c7/molce-45-8-522-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13f2/9385571/5a457c4e0cc4/molce-45-8-522-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13f2/9385571/c716b40cd03b/molce-45-8-522-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13f2/9385571/851591416c59/molce-45-8-522-f4.jpg

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Identification of a Seven-lncRNA-mRNA Signature for Recurrence and Prognostic Prediction in Relapsed Acute Lymphoblastic Leukemia Based on WGCNA and LASSO Analyses.基于 WGCNA 和 LASSO 分析的复发急性淋巴细胞白血病复发和预后预测的七个长链非编码 RNA-mRNA 特征的鉴定。
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