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

Z-DNA gene function human diseases human endogenous retrovirus long terminal repeat elements

Journal

Molecules and cells
ISSN: 0219-1032
Titre abrégé: Mol Cells
Pays: Korea (South)
ID NLM: 9610936

Informations de publication

Date de publication:
31 Aug 2022
Historique:
received: 11 04 2022
revised: 16 05 2022
accepted: 31 05 2022
entrez: 11 8 2022
pubmed: 12 8 2022
medline: 13 8 2022
Statut: ppublish

Résumé

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

Identifiants

pubmed: 35950452
pii: molcells.2022.0060
doi: 10.14348/molcells.2022.0060
pmc: PMC9385571
doi:

Substances chimiques

DNA, Z-Form 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

522-530

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Auteurs

Du Hyeong Lee (DH)

Department of Integrated Biological Sciences, Pusan National University, Busan 46241, Korea.
Institute of Systems Biology, Pusan National University, Busan 46241, Korea.
These authors contributed equally to this work.

Woo Hyeon Bae (WH)

Department of Integrated Biological Sciences, Pusan National University, Busan 46241, Korea.
Institute of Systems Biology, Pusan National University, Busan 46241, Korea.
These authors contributed equally to this work.

Hongseok Ha (H)

Division of Life Sciences, Korea University, Seoul 02841, Korea.
These authors contributed equally to this work.

Eun Gyung Park (EG)

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

Yun Ju Lee (YJ)

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

Woo Ryung Kim (WR)

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

Heui-Soo Kim (HS)

Department of Biological Sciences, College of Natural Sciences, Pusan National University, Busan 46231, Korea.
Institute of Systems Biology, Pusan National University, Busan 46241, Korea.

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