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Sung,
your post is commendable, an advanced treatise to extend the narrowness of
the limited model-view even in the 'more advanced' version of the obsolete views
(definitions).
As usual: I have 2 questions.
1. Isn't there a chance for a 'reversed' Prigogine effect: to
'assipate'(!!) factors INTO the process from the ambience, maybe at least
not not yet recognised, or even discovered?
2. If there is 'mechanically' stored energy in the
(unassigned?) DNA stretches, is such energy capable of being put to
use from DEAD tissue? (I think of some answers: "dead" may mean that it
lost such capability together with other transformations, the other is the fact
that transplantations are feasible. I may be lay-wrong.)
Respects
John M
----- Original Message -----
Sent: Wednesday, July 09, 2008 11:54
PM
Subject: What is a gene? A dynamic &
triadic definition of a gene
(Yaneer, if it is not too late, please replace my previous post
with this one. Thanks. Sung)
The most widely accepted
definition of a gene during the past four decades has been a stretch of DNA
that codes for a protein. Although this simple definition of a gene served
well for the 20th-century molecular biology and genetics, the new data that
have been emerging since the mid-1990's (when DNA microarrays were
invented) have made the protein-centered definition of a gene obsolete
[1,2,3]. A new definition proposed by Gerstein and his coworkers at Yale
now includes as a gene those DNA regions that code for RNA as well
[2]:
"A gene is a union of genomic sequences
encoding a coherent set of potentially
overlapping functional
products."
. . . . . (1)
The important phrase here is "functional products", by
which the authors mean proteins and RNA molecules that are biologically
active.
The new definition of a gene given in (1) was motivated by the
recent unexpected finding [1,3] that a large portion of the human genome
(about 30% of the DNA mass), although not coding for any proteins,
nevertheless code for RNA molecules whose functions have not yet all been
characterized.
There are two aspects to the definition of a gene given
in (1) that I believe require revisions:
i) It is too
static, being based solely on gene "products", i.e., proteins and RNA,
which are "equilibrium structures". According to Prigogine
(917-2003)[4], there are two fundamental classes of structures in nature --
equilibrium (e.g., rocks, chairs, DNA double helix, nucleotide or amino
acid sequences) and dissipative structures (e.g., the flame of a candle,
all sorts of gradients, action potentials, gene expression profiles). One
convenient way to distinguish dissipative structures from equilibrium
structures is to remember that, when energy input is stopped, the former
disappears but the latter remains. For example, when a computer is turned
off, the primary memory (a dissipative structure) in CPU disappears but the
secondary memory (an equilibrium structure) in the hard disk
remains.
ii) It excludes those DNA regions that regulate gene
expression (called promoters, enhancers, silencers, etc.) without producing
any proteins or RNA. In other words, Gerstein et al's definition of a gene
excludes "dissipative structures" which would include all regulatory
processes in the living cell. This is what Gerstein et al state
[2]:
"Although regulatory regions are important for
gene expression, we suggest that they should not
be considered in deciding whether multiple
products belong to the same gene. . . .
" . . . . . . . . . . . (2)
To
remedy these perceived shortcomings, I suggest that the concept
of "dissipative structures" [4] be incorporated into the definition of a
gene itself. One way to do this is as follows:
"A
gene is a DISSIPATIVE STRUCTURE that embodies (or
stores) not only genetic information (in the form of
a nucleotide sequence of DNA regions) but also
mechanical energy (in the form of conformationally
strained DNA regions) generated from chemical
reactions catalyzed by
enzymes." . . . .
. . . . . . . . . . . . . . . (3)
The fact that active regions of DNA
carry mechanical energy, for example, in the form of DNA supercoils, has
been well established [5]. Such mechanical energy stored in DNA has
been variously referred to as conformons [6] and "Stress-Induced Duplex
Destabilizations" or SIDDS [5].
The definition of a gene given in (3)
is tantamount to postulating that a gene is a molecular machine composed of
DNA segments and associated proteins that stores mechanical energy
generated from chemical reactions and uses this energy to transcribe its
sequence information into RNA molecules whenever and wherever needed in the
cell for a right duration of time.
The definition of a gene given by
(1) can be made compatible with the definition given by (3) if we make the
following two postulates:
"The whole DNA
carries three kinds of genes -- p-genes
coding for proteins, r-genes coding for RNA,
and d-genes coding for DNA molecules."
. . . . . . (4)
The existence of d-genes is self-evident, since DNA
serves as the template for its own replication and this ability of DNA is
heritable from one cell generation to the
next.
"DNA carries not only
genetic/sequence information but also
the mechanical energy (called conformons or
SIDDS) to power gene
expression. . . . . . . . . . . . . .
. (5)
In other words, by combining the dissipative structure
concept of Prigogine [4] and the conformon concept introduced in molecular
biology more than three decades ago (reviewed in [6]), a new definition of
a gene can be formulated in two parts as
follows:
i) "DNA carries three kinds of genes, each
coding for proteins (p-genes), RNA
molecules (r-genes), and DNA molecules
(d-genes)." . . . . . . . . . . . . . . . .(6)
ii) "DNA
stores mechanical energy in the form
of conformons or SIDDS that
powers the spatiotemporally
organized motions of chromatins
in order to express p-, r- and d-genes
in response to the signals
received from the
cytosol."
. . . . . . . . . . . (7)
Statement (6) can be regarded as a definition
of terms that are compatible with facts, and what is original in the
proposed 'triadic' definition of a gene is contained in Statement (7) in
the concept of conformons [6] or SIDDS [5]. Conformons are defined as the
sequence-specific conformational strains of biopolymers that carry 'ordered
energy' to power goal-directed molecular motions [6]. The first
direct experimental evidence for conformons in DNA was provided by DNA
supercoils [5] and for conformons in proteins by the single-molecule
measurements of myosin motions along actin filament [7]. Also, Statement
(6) deals with the informational aspects of a gene, while Statement (7) is
concerned primarily with the energetic aspect of a gene, consistent with
the information-energy complementarity principle believed to underlie all
self-orgnaizng processes in nature [8].
With all the
best.
Sung
___________________________________________ Sungchul
Ji, Ph.D. Department of Pharmacology and Toxicology Rutgers
University Piscataway, N.J., 08855
References:
[1] Pearson, H. (20056). Genetics: What is a gene? Nature
441:398-401. [2] Gerstein, M. B. et al. (2007). What is a
gene, post-ENCODE? History and updated definition. Genome Research
17:669-681. [3] Greally, J. M. (2007). Genomics: Encyclopedia
of human DNA. Nature 447: 782-783. [4] Prigogine, I.
(1977). Dissipative Structures and Biological Order. Adv. Biol.
Med. Phys. 16:99-113. [5] Benham, C. J. (1996). Duplex
Destabilization in Supercoiled DNA is Predicted to Occur at Specific
Transcriptional Regulatory Regions. J. Mol. Biol.
255:425-434. [6] Ji, S. (2000). Free energy and
information content of Conformons in proteins and DNA. BioSystems 54:
107-130. [7] Ishijima, A., Kojima, H., Higuchi, H., Harada,
Y., Funatsu, T. and Yanagida, T. (1998). Simultaneous measurement of
chemical and mechanical reaction. Cell 70:161-171.
[8] Ji, S. (2002). The Bhopalator: An Information/Energy Dual Model of the
Living Cell (II). Fundamenta Informaticae 49(1-3),
147-165.
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