A novel hypervariable variable number tandem repeat in the dopamine transporter gene (SLC6A3)

Author:

Apsley Abner T12ORCID,Domico Emma R1ORCID,Verbiest Max A345ORCID,Brogan Carly A1,Buck Evan R1ORCID,Burich Andrew J6,Cardone Kathleen M1,Stone Wesley J1,Anisimova Maria35ORCID,Vandenbergh David J1278ORCID

Affiliation:

1. Department of Biobehavioral Health, The Pennsylvania State University

2. The Molecular, Cellular and Integrative Biosciences Program, The Pennsylvania State University

3. Institute of Computational Life Science, School of Life Sciences and Facility Management, Zürich University of Applied Sciences

4. Department of Molecular Life Sciences, Faculty of Science, University of Zurich, Zurich, Switzerland

5. Swiss Institute of Bioinformatics, Lausanne, Switzerland

6. Department of Information Science and Technologies - Applied Data Sciences, The Pennsylvania State University

7. Institute of the Neurosciences, The Pennsylvania State University

8. The Bioinformatics and Genomics Program, The Pennsylvania State University

Abstract

The dopamine transporter gene,SLC6A3, has received substantial attention in genetic association studies of various phenotypes. Although some variable number tandem repeats (VNTRs) present inSLC6A3have been tested in genetic association studies, results have not been consistent. VNTRs inSLC6A3that have not been examined genetically were characterized. The Tandem Repeat Annotation Library was used to characterize the VNTRs of 64 unrelated long-read haplotype-phasedSLC6A3sequences. Sequence similarity of each repeat unit of the five VNTRs is reported, along with the correlations of SNP–SNP, SNP–VNTR, and VNTR–VNTR alleles across the gene. One of these VNTRs is a novel hyper-VNTR (hyVNTR) in intron 8 ofSLC6A3, which contains a range of 3.4–133.4 repeat copies and has a consensus sequence length of 38 bp, with 82% G+C content. The 38-base repeat was predicted to form G-quadruplexes in silico and was confirmed by circular dichroism spectroscopy. In addition, this hyVNTR contains multiple putative binding sites for PRDM9, which, in combination with low levels of linkage disequilibrium around the hyVNTR, suggests it might be a recombination hotspot.

Funder

Biobehavioral Health Department, Pennsylvania State University

HHS | NIH | National Institute on Aging

Publisher

Life Science Alliance, LLC

Subject

Health, Toxicology and Mutagenesis,Plant Science,Biochemistry, Genetics and Molecular Biology (miscellaneous),Ecology

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Advances in the discovery and analyses of human tandem repeats;Emerging Topics in Life Sciences;2023-10-31

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