TY - JOUR
T1 - DNA Looping Mediated by Site-Specific SfiI-DNA Interactions
AU - Vemulapalli, Sridhar
AU - Hashemi, Mohtadin
AU - Kolomeisky, Anatoly B.
AU - Lyubchenko, Yuri L.
N1 - Funding Information:
This work was supported by NSF grant MCB- 1941049/1941106 to Y.L.L. A.B.K. acknowledges the support from the Welch Foundation (C-1559), from the NSF (CHE-1953453 and MCB-1941106), and from the Center for Theoretical Biological Physics sponsored by the NSF (PHY-2019745). We thank L. Shlyakhtenko (University of Nebraska Medical Center) for useful insights and all of the Y.L.L lab members for their fruitful discussions. The authors thank Tommy D. Stormberg (University of Nebraska Medical Center) for proofreading the manuscript. The UNMC Genomics Core Facility receives partial support from the NIGMS INBRE - P20GM103427-19, as well as the NCI center grant for Fred & Pamela Buffett Cancer Center - P30CA036727.
Publisher Copyright:
© 2021 American Chemical Society.
PY - 2021/5/13
Y1 - 2021/5/13
N2 - Interactions between distant DNA segments play important roles in various biological processes, such as DNA recombination. Certain restriction enzymes create DNA loops when two sites are held together and then cleave the DNA. DNA looping is important during DNA synapsis. Here we investigated the mechanisms of DNA looping by restriction enzyme SfiI by measuring the properties of the system at various temperatures. Different sized loop complexes, mediated by SfiI-DNA interactions, were visualized with AFM. The experimental results revealed that small loops are more favorable compared to other loop sizes at all temperatures. Our theoretical model found that entropic cost dominates at all conditions, which explains the preference for short loops. Furthermore, specific loop sizes were predicted as favorable from an energetic point of view. These predictions were tested by experiments with transiently assembled SfiI loops on a substrate with a single SfiI site.
AB - Interactions between distant DNA segments play important roles in various biological processes, such as DNA recombination. Certain restriction enzymes create DNA loops when two sites are held together and then cleave the DNA. DNA looping is important during DNA synapsis. Here we investigated the mechanisms of DNA looping by restriction enzyme SfiI by measuring the properties of the system at various temperatures. Different sized loop complexes, mediated by SfiI-DNA interactions, were visualized with AFM. The experimental results revealed that small loops are more favorable compared to other loop sizes at all temperatures. Our theoretical model found that entropic cost dominates at all conditions, which explains the preference for short loops. Furthermore, specific loop sizes were predicted as favorable from an energetic point of view. These predictions were tested by experiments with transiently assembled SfiI loops on a substrate with a single SfiI site.
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U2 - 10.1021/acs.jpcb.1c00763
DO - 10.1021/acs.jpcb.1c00763
M3 - Article
C2 - 33914533
AN - SCOPUS:85106465781
SN - 1520-6106
VL - 125
SP - 4645
EP - 4653
JO - Journal of Physical Chemistry B
JF - Journal of Physical Chemistry B
IS - 18
ER -