Dear Sung,

Very encouraging the discussion of the difficulties human perception poses
while trying to consolidate opposites.

The existence of the mental image is built on contrasts, so no wonder we
find it hard to get a good grip on the mechanisms at work consolidating
contradictions.

To the opposites we work on :

tree vs. forest,
top vs. bottom,
little vs. big,

could we also add:

background vs. foreground,
across the flow vs. along the flow of time,
commutative vs. sequenced?

If so, there appear some encouraging hints, that a rational methodology has
been found to consolidate opposites.

Karl

Sungchul Ji <s...@pharmacy.rutgers.edu> schrieb am Do., 3. Mai 2018 18:01:

> Hi Stan,
>
>
> True.  Our brain seems to have many limitations, one of which is our
> inability to see the forest and the trees simultaneously.
>
>
> It is interesting to note that we cannot measure (or at least not easy to
> measure) particles and waves of quons  (or quantum objects) simultaneously
> either,  although there are occasional claims asserting otherwise. Here we
> have two entities, A and B, that are not compositionally related (i.e., A
> is not a part of B) as are trees and the forest, but "complementarily"
> related (i.e., A^B, read A or B, depending on measurement) and hence does
> not involve any hierarchy.
>
>
> All the best.
>
>
> Sung
>
> ------------------------------
> *From:* Fis <fis-boun...@listas.unizar.es> on behalf of Stanley N Salthe <
> ssal...@binghamton.edu>
> *Sent:* Sunday, April 29, 2018 9:49 AM
> *To:* fis
> *Subject:* Re: [Fis] Fw: The 'Shirasawa phenomenon' or the 'Shirasawa
> effect"
>
> Sung -- regarding:
>
> The reason epigenetics (defined here as the process of inheritance without
> imlplicating any changes in the nucleotide sequences of DNA)  was not
> mentioned in my previous post is because I was mainly interested in the
> bottom-up (from micro to macro) mechanism of genetics, not the top-down
> (from macro to micro) mechanism.  It is interesting to note that our brain
> seems unable to handle both bottom-up and top-down mechanisms
> simultaneously, perhaps it may have something to do with the fact that we
> have two brain hemispheres (Yin and Yang) but only one vocal cord (the
> Dao).
>
> It is interesting that I early realized the difficulty many folks have
> with visualizing at one time both the top-down AND bottom-up aspects of the
> compositional hierarchy:
>                 [large scale constraints -> [activity in focus <- [small
> scale affordances]]]
>
> Perhaps your suggestion is involved here as well!
>
> STAN
>
> On Sat, Apr 28, 2018 at 5:17 PM, Sungchul Ji <s...@pharmacy.rutgers.edu>
> wrote:
>
> Hi Arthur and  FISers,
>
> Thank you for asking an important question. The reason epigenetics
> (defined here as the process of inheritance without imlplicating any
> changes in the nucleotide sequences of DNA)  was not mentioned in my
> previous post is because I was mainly interested in the bottom-up (from
> micro to macro) mechanism of genetics, not the top-down (from macro to
> micro) mechanism.  It is interesting to note that our brain seems unable to
> handle both bottom-up and top-down mechanisms simultaneously, perhaps it
> may have something to do with the fact that we have two brain hemispheres
> (Yin and Yang) but only one vocal cord (the Dao).
>
> One way to integrate the bottom-up and top-down mechanisms underlying
> genetic phenomenon may be to invoke the principle of vibrational resonance
> -- to view both the micro-scale DNA and  the macro-scale environment of
> organisms as vibrational systems or systems of oscillators that can
> exchange information and energy through the well-known mechanisms of
> resonance (e.g., the resonance between the oscillatory motions of the swing
> and the arms of the mother; both motions must have same
> frequencies. otherwise the child will not swing).  According to the
> Fourier theorem, any oscillatory motions of DNA including very low
> frequencies can be generated by linear combinations of  very fast
> covalent bond vibrations in  DNA and  hence can be coupled to slow
> oscillatory motions of the environment, e.g., musical sounds. If this view
> is correct, music can affect, DIRECTLY (i.e., unmediated by the auditory
> system of the brain), the molecular motions of DNA in every cell in our
> body.  In other words, we can hear music not only through our ears but also
> through our whole body including blood.  Because of the patent  issue, I
> cannot reveal the experimental evidence supporting this claim, but, indue
> course, I hope to share with you the scientific evidence we obtained
> recently.
>
> In conclusion, it may be that  the yin-yang doctrine of the Daoist
> philosophy (or any other equivalent principles) applies here, since
> molecular genetics and epigenetics may constitute  the
> irreconcilable opposites:
>
> "Genetics has two complementary aspects -- molecular genetics and
> epigenetics."
>
> "Molecular genetics and epigenetics are the complementary
> aspects of genetics."
>
> "Genetic phenomena can be accounted for in two irreconcilably opposite
> manner with equal validity -- through the bottom-up (or reductionistic) or
> the top-down  (or holistic) approaches."
>
> The last statement would help avoid many wasteful debates in the field of
> genetics.
>
>  If you have any questions or corrections, please let me know.
>
> Sung
>
>
>
>
>
>
>
>
>
>
>
> ------------------------------
> *From:* Arthur Wist <arthur.w...@gmail.com>
> *Sent:* Friday, April 27, 2018 6:48 PM
> *To:* Sungchul Ji; FIS FIS
> *Cc:* sbur...@proteomics.rutgers.edu; Sergey Petoukhov;
> ole2001@med.cornell; dani...@shirasawa-acl.net; Sungchul Ji;
> x...@chemistry.harvard.edu; n...@princeton.edu
> *Subject:* Re: [Fis] Fw: The 'Shirasawa phenomenon' or the 'Shirasawa
> effect"
>
> Hi,
>
> Just a short note to first of all say thank you, I've find this very
> helpful to know albeit I can't point to a direct application. Secondly
> however, I do wonder: Why & how come you neglected to - in either an
> inclusionary or exclusionary manner - address any potential epigenetic
> mechanisms?
>
> Kind regards,
>
>
> Arthur
>
> On 20 April 2018 at 19:32, Sungchul Ji <s...@pharmacy.rutgers.edu> wrote:
> > Hi,
> >
> >
> > I am forwarding a slightly modified version of my previous post with the
> > same title which was rejected by the FIS list due to the heavy
> attachments.
> > The most significant addition is written in green.  The removed
> attachments
> > are now replaced by their web addresses from which they can be downloaded
> > free of charge.
> >
> >
> > Best.
> >
> >
> > Sung
> >
> > ________________________________
> > From: Sungchul Ji
> > Sent: Thursday, April 19, 2018 11:02 AM
> > To: FIS FIS
> > Cc: Sergey Petoukhov; dani...@shirasawa-acl.net; John Stuart Reid;
> sayer ji;
> > sji.confor...@gmail.com; x...@chemistry.harvard.edu;
> > sbur...@proteomics.rutgers.edu; n...@princeton.edu
> > Subject: The 'Shirasawa phenomenon' or the 'Shirasawa effect"
> >
> >
> > Hi FISers,
> >
> >
> > In 2003, Takuji Shirasawa and his coworkers [1] found that mutating
> certain
> > amino acids in the hemoglobin molecule (Hb) in mice produced the
> following
> > effects:
> >
> > (1) increase O_2 consumption and CO_2 production,
> >
> > (2) the conversion of the muscle histology from a fast glycolytic to a
> fast
> > oxidative type,
> >
> > (3) a mild anemia, and
> >
> > (4) faster running speed.
> >
> >
> > In other words, Shirasawa et al provided a concrete example of molecular
> > changes (e.g., amino acid mutations in Hb)  leading to (or associated
> with)
> > macroscopic physiological changes in whole animals (e.g., anemia,
> running
> > behavior, etc.).  For the convenience of discussions, I am taking the
> > liberty of referring to this finding as the "Shirasawa et al.
> > phenomenon/effect" or, more briefly, the "Shirasawa phenomenon/effect"
> which
> > may be viewed as the macroscopic version of the Bohr effect [2].
> >
> >
> > The 'Shirasawa phenomenon/effect' is not limited to hemoglobin.  There
> are
> > now many similar phenomena found in the fields of voltage-gated ion
> > channels, i.e., molecular changes in the amino acid sequences of ion
> channel
> > proteins leading to (or associated with) macroscopic effects on the human
> > body called diseases [3].
> >
> >
> > Although the current tendency among practicing molecular biologists and
> > biophysicists would be to explain away what is here called the Shirasawa
> > phenomenon in terms of the microscopic changes "causing" the macroscopic
> > phenomenon in a 1:1 basis, another possibility is that the microscopic
> > changes "cause" a set of other microscopic changes at the DNA molecular
> > level which in turn cause a set of macroscopic changes", in a
> many-to-many
> > fashion.
> >
> >
> > Current trend:  Microscopic change (Hb mutation) --------->  Macroscopic
> > change 1 (Oxygen affinity change of blood) ---------> Macroscopic change
> 2
> > (O_2 metabolism, anemia, running behavior)
> >
> >
> >
> > Althernative mechanism:  Microscopic change 1 (Hb mutation) ------->
> > Microscopic change 2 (Changes in the standing waves in DNA) ------->
> > Multiple macroscopic changes (O_2 metabolism, anemia, muscle cell
> > histological changes).
> >
> >
> > The alternative mechanism proposed here seems to me to be more consistent
> > with the newly emerging models of molecular genetics [4] and
> single-molecule
> > enzymology [5, 6].
> >
> >
> >
> > Since the 'Shirasawa phenomenon/effect' evidently implicates information
> > transfer from the microscale to the macroscale, it may be of interest to
> > many information theoreticians in this group.   If you have any
> questions,
> > comments, or suggestions, please let me know.
> >
> >
> > All the best.
> >
> >
> > Sung
> >
> >
> >
> > References:
> >
> >    [1] Shirasawa, T., et al. (2003).  Oxygen Affinity of Hemoglboin
> > Regulaters O_2 Comsumtion, Metabolism, and Physical Activity.  J. Biol.
> > Chem. 278(7): 5035-5043.  PDF at
> >
> https://na01.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.jbc.org%2Fcontent%2F278%2F7%2F5035.full.pdf&data=02%7C01%7Csji%40pharmacy.rutgers.edu%7Cb134e6f0f18640a1578608d5ac911871%7Cb92d2b234d35447093ff69aca6632ffe%7C1%7C1%7C636604661553806634&sdata=sNOsN%2BTGxWSKHNzVWNJXDW3dU6tveVfKfNPaV%2Bcv3e4%3D&reserved=0
> >
> >    [2] The Bohr effect.
> https://na01.safelinks.protection.outlook.com/?url=https%3A%2F%2Fen.wikipedia.org%2Fwiki%2FBohr_effect&data=02%7C01%7Csji%40pharmacy.rutgers.edu%7Cb134e6f0f18640a1578608d5ac911871%7Cb92d2b234d35447093ff69aca6632ffe%7C1%7C1%7C636604661553806634&sdata=T%2Fl5fXUzb4RN0RUwpLBwASDExyceUPasgf%2BaJhmraJw%3D&reserved=0
> >    [3] Huang W, Liu M, S Yan F, Yan N. (2017).  Structure-based
> assessment
> > of disease-related mutations in human voltage-gated sodium channels.
> Protein
> > Cell. 8(6):401-438. PDF at
> https://na01.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.ncbi.nlm.nih.gov%2Fpubmed%2F28150151&data=02%7C01%7Csji%40pharmacy.rutgers.edu%7Cb134e6f0f18640a1578608d5ac911871%7Cb92d2b234d35447093ff69aca6632ffe%7C1%7C1%7C636604661553806634&sdata=QERnpZll0BGSz20njXkWQZaNzKCt1EenJx7X7O3Qak4%3D&reserved=0
> >
> >    [4] Petoukhov, S. V. (2016).  The system-resonance approach in
> modeling
> > genetic structures. BioSystems 139: 1–11. PDF at
> >
> https://na01.safelinks.protection.outlook.com/?url=https%3A%2F%2Fwww.sciencedirect.com%2Fscience%2Farticle%2Fpii%2FS0303264715001732&data=02%7C01%7Csji%40pharmacy.rutgers.edu%7Cb134e6f0f18640a1578608d5ac911871%7Cb92d2b234d35447093ff69aca6632ffe%7C1%7C1%7C636604661553806634&sdata=%2FzkdwHLVCa5ROQXJmhmEho7qNUNAky8L1gFjOuee%2B1Y%3D&reserved=0
> >
> >    [5] Lu, H. P., Xun, L. and Xie, X. S. (1998) Single-Molecule Enzymatic
> > Dynamics. Science 282:1877-1882.  PDF at
> >
> https://na01.safelinks.protection.outlook.com/?url=http%3A%2F%2Fwww.jbc.org%2Fcontent%2F274%2F23%2F15967.short&data=02%7C01%7Csji%40pharmacy.rutgers.edu%7Cb134e6f0f18640a1578608d5ac911871%7Cb92d2b234d35447093ff69aca6632ffe%7C1%7C1%7C636604661553806634&sdata=MiyaHdch%2B0%2BbaKVZ6xKGz1WJ22%2BKBlLrGpX2QkxvmXs%3D&reserved=0
> >    [6] Ji, S. (2017). RASER Model of Single-Molecule Enzyme Catalysis and
> > Its Application to the Ribosome Structure and Function. Arch Mol. Med &
> Gen
> > 1:104. PDF at
> https://na01.safelinks.protection.outlook.com/?url=http%3A%2F%2Fhendun.org%2Fjournals%2FAMMG%2FPDF%2FAMMG-18-1-104.pdf&data=02%7C01%7Csji%40pharmacy.rutgers.edu%7Cb134e6f0f18640a1578608d5ac911871%7Cb92d2b234d35447093ff69aca6632ffe%7C1%7C1%7C636604661553806634&sdata=uviYFoPZJ84kVeHTn6CorCcn1Z6mt6Va7Zni18AJ7o4%3D&reserved=0
> >
> >
> >
> >
> >
> >
> >
> >
> > _______________________________________________
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