Page 42
allied
academies
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.comMolecular Biology & Heart Congress 2018, Volume 29
DOI: 10.4066/biomedicalresearch-C8-023