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      Parity-dependent hairpin configurations of repetitive DNA sequence promote slippage associated with DNA expansion

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          Significance

          We found that TGGAA DNA repeats, which are involved in the neurological disease spinocerebellar ataxia 31, are capable of assuming two different hairpin structures depending on repeat number parity. We determined the interconversion kinetics by single-molecule spectroscopy and probed the interconversion mechanism through elucidation of the TGGAA repeat stem structure. Our results suggest that the two hairpin structures interconvert through motion slippage, and the process can be explained by the overall stem stability and local destabilization of the kinked GGA motif. Divalent cations and stem length affected the equilibrium and kinetics of slippage. Our findings suggest a mechanism by which a binary dynamic property of DNA repeats may affect repeat expansion and may be applicable to other repetitive DNA systems.

          Abstract

          Repetitive DNA sequences are ubiquitous in life, and changes in the number of repeats often have various physiological and pathological implications. DNA repeats are capable of interchanging between different noncanonical and canonical conformations in a dynamic fashion, causing configurational slippage that often leads to repeat expansion associated with neurological diseases. In this report, we used single-molecule spectroscopy together with biophysical analyses to demonstrate the parity-dependent hairpin structural polymorphism of TGGAA repeat DNA. We found that the DNA adopted two configurations depending on the repeat number parity (even or odd). Transitions between these two configurations were also observed for longer repeats. In addition, the ability to modulate this transition was found to be enhanced by divalent ions. Based on the atomic structure, we propose a local seeding model where the kinked GGA motifs in the stem region of TGGAA repeat DNA act as hot spots to facilitate the transition between the two configurations, which may give rise to disease-associated repeat expansion.

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          Mechanisms underlying structural variant formation in genomic disorders.

          With the recent burst of technological developments in genomics, and the clinical implementation of genome-wide assays, our understanding of the molecular basis of genomic disorders, specifically the contribution of structural variation to disease burden, is evolving quickly. Ongoing studies have revealed a ubiquitous role for genome architecture in the formation of structural variants at a given locus, both in DNA recombination-based processes and in replication-based processes. These reports showcase the influence of repeat sequences on genomic stability and structural variant complexity and also highlight the tremendous plasticity and dynamic nature of our genome in evolution, health and disease susceptibility.
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            Is Open Access

            Conformational analysis of nucleic acids revisited: Curves+

            We describe Curves+, a new nucleic acid conformational analysis program which is applicable to a wide range of nucleic acid structures, including those with up to four strands and with either canonical or modified bases and backbones. The program is algorithmically simpler and computationally much faster than the earlier Curves approach, although it still provides both helical and backbone parameters, including a curvilinear axis and parameters relating the position of the bases to this axis. It additionally provides a full analysis of groove widths and depths. Curves+ can also be used to analyse molecular dynamics trajectories. With the help of the accompanying program Canal, it is possible to produce a variety of graphical output including parameter variations along a given structure and time series or histograms of parameter variations during dynamics.
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              Repeat instability as the basis for human diseases and as a potential target for therapy.

              Expansions of repetitive DNA sequences cause numerous human neurological and neuromuscular diseases. Ongoing repeat expansions in patients can exacerbate disease progression and severity. As pathogenesis is connected to repeat length, a potential therapeutic avenue is to modulate disease by manipulating repeat expansion size--targeting DNA, the root-cause of symptoms. How repeat instability is mediated by DNA replication, repair, recombination, transcription and epigenetics may explain its contribution to pathogenesis and give insights into therapeutic strategies to block expansions or induce contractions.
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                Author and article information

                Journal
                Proc Natl Acad Sci U S A
                Proc. Natl. Acad. Sci. U.S.A
                pnas
                pnas
                PNAS
                Proceedings of the National Academy of Sciences of the United States of America
                National Academy of Sciences
                0027-8424
                1091-6490
                5 September 2017
                21 August 2017
                : 114
                : 36
                : 9535-9540
                Affiliations
                [1] aDepartment of Chemistry, National Taiwan Normal University , Taipei, Taiwan 116;
                [2] bInstitute of Genomics and Bioinformatics, National Chung Hsing University , Taichung, Taiwan 402;
                [3] cInstitute of Biomedical Sciences, Academia Sinica , Taipei, Taiwan 115;
                [4] dInstitute of Biochemistry, National Chung-Hsing University , Taichung, Taiwan 402
                Author notes
                2To whom correspondence may be addressed. Email: irenlee@ 123456ntnu.edu.tw or mhho@ 123456dragon.nchu.edu.tw .

                Edited by Taekjip Ha, Johns Hopkins University, Baltimore, MD, and approved July 31, 2017 (received for review May 26, 2017)

                Author contributions: I-R.L. and M.-H.H. designed research; T.-Y.H., Y.-F.K., C.-H.C., C.-W.N., and H.-Y.H. performed research; T.-Y.H., C.-k.C., Y.-F.K., C.-H.C., C.-W.N., H.-Y.H., N.-J.H., L.-C.H., S.-H.C., I-R.L., and M.-H.H. analyzed data; and C.-k.C., I-R.L., and M.-H.H. wrote the paper.

                1T.-Y.H. and C.-k.C. contributed equally to this work.

                Author information
                http://orcid.org/0000-0002-3864-1896
                http://orcid.org/0000-0001-5655-6049
                Article
                PMC5594692 PMC5594692 5594692 201708691
                10.1073/pnas.1708691114
                5594692
                28827328
                9cd8442b-2b23-4419-b258-bafda886c464
                History
                Page count
                Pages: 6
                Funding
                Funded by: Ministry of Science and Technology, Taiwan (MOST) 501100004663
                Award ID: 105-2113-M-003-009-MY2
                Funded by: Ministry of Science and Technology, Taiwan (MOST) 501100004663
                Award ID: 103-2113-M-005-007-MY3
                Categories
                Physical Sciences
                Biophysics and Computational Biology
                Biological Sciences
                Biophysics and Computational Biology

                DNA tandem repeats,single-molecule spectroscopy,DNA slippage,X-ray crystallography

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