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Journal of Biomedical Research | Volume: 29

November 19-20, 2018 | Paris, France

Molecular Biology, Tissue Science and Regenerative Medicine

International Conference on

Joint Event

&

4

th

World Heart Congress

The centres of premeltons signal the beginning and ends of genes

Henry M Sobell

University of Rochester, USA

P

remeltons are examples of emergent structures (i.e.,

structural solitons) that arise spontaneously in DNA due

to the presence of nonlinear excitations in its structure. They

are of two kinds: B-B or A-A premeltons form at specific

DNA-regions to nucleate site-specific DNA melting. These are

stationary and being globally nontopological, undergo breather

motions that allow drugs and dyes to intercalate into DNA. B-A

or A-B premeltons, on the other hand, are mobile and being

globally topological, act as phase-boundaries transforming B-

into A- DNA during the structural phase-transition. They are

not expected to undergo breather-motions. A key feature of

both types of premeltons is the presence of an intermediate

structural-form in their central regions (proposed as being a

transition-state intermediate in DNA-melting and in the B-

to A- transition), which differs from either A- DNA or B- DNA

called beta-DNA, this is both metastable and hyperflexible

and contains an alternating sugar-puckering pattern along

the polymer-backbone combined with the partial-unstacking

(in its lower energy-forms) of every other base-pair. Beta-

DNA is connected to either B- or to A- DNA on either side by

boundaries possessing a gradation of nonlinear structural-

change, these being called the kink and the antikink regions.

The presence of premeltons in DNA leads to a unifying theory

to understand much of DNA physical-chemistry and molecular-

biology. The premeltons are predicted to define the 5’ and 3’

ends of genes in naked-DNA and DNA in active-chromatin,

this having important implications for understanding physical

aspects of the initiation, elongation and termination of RNA-

synthesis during transcription. For these and other reasons,

the model will be of broader interest to the general audience

working in these areas. The model explains a wide variety of

data and carries within it several experimental predictions all

readily testables as will be described in my talk.

e:

sobell@localnet.com

Molecular Biology & Heart Congress 2018, Volume 29

DOI: 10.4066/biomedicalresearch-C8-023