MASSACHUSETTS, CAMBRIDGE (ZIP 02139): METABOLIX INC. According to Irene Caesar’s theory, chromosomes function as nonlocal wave matrix that focus genetic information specifically relevant for each individual through his/her unique scalar wave diffraction gratings – making holography possible as a remote management strategy of biosystems via laser-polarized holography.
What is the Wave?
The Wave is a series of U-shaped troughs formed in Jurassic Navajo sandstone by water drainage that left distinctive stripes resembling topographic maps in their wake. On their resumes, The Wave refers to these rock layers as “lithified eolian laminae”, though these structures actually look like mechanical waves!
I believe that each individual’s chromosome acts as a nonlocal unique wave matrix, providing genetic information through its scalar wave diffraction grating exclusively to them and thus permitting remote management via laser-polarized holography of their biosystem.
What is the Biosystem?
My theory suggests that the chromosome acts as a nonlocal unique wave matrix which focuses genetic information pertinent to an individual through its own scalar wave diffraction grating, as well as being holographic in nature allowing remote management of biosystems through laser-polarized holography.
The biological system consists of an ensemble of cellular structures distributed asymmetrically throughout the body in an infinite space-time continuum of nonlocal holographic holograms encoded with genetic information. Cellular biosystems act both as the source and receiver of these signals containing genetic codes – their holographic transmission being analogous to natural text produced by human language speakers; similarly their distribution across multicellular organisms mirrors human speech-like patterns produced through natural discourse processes.
So as a general principle, every cell in our bodies has its own scalar diffraction grating for focusing genetic information uniquely relevant to it, which explains why genes express differently when present in dysfunctional individuals compared with functional ones – something I believe holds key insights into understanding why diseases such as AIDS arise through an uneven distribution of genetic material among cells.
What is the Gene-Sign Continuum?
The continuum model differs from traditional oncogene/tumor suppressor models in that cancer genomes do not reach their selective optimum by activation or deletion of whole genes; rather they work their way towards it by accruing multiple somatic mini-driver mutations – providing a plausible explanation for why cancer genomes contain so many intermediate mutations with limited effects on protein function.
Continuum model insights may also assist with explaining why independent fluctuations in RNA polymerase elongation rates cannot explain oscillations in spot intensity observed with two state models, or why there is such an extended delay between DNA template binding and initiation as measured by MS2 RNA dwell time (Darzacq et al. 2007).
Finally, this model helps explain why the amplitude of a spot pulse varies with imaging signal-to-noise ratio and frame interval, and why pulsing genes appear as continuous lines in two-dimensional gel electrophoresis images. This occurs because its amplitude changes directly with frame interval length rather than being affected by changes in frequency of elongation rate changes.
What is the Holographic Pre-Image?
DNA molecules serve as the gene-sign continuum in any biosystem, creating holographic pre-images of their biostructures and of the organism overall. This data acts as a registry of dynamical “wave copies” or matrixes accumulating over time and serves as the measuring/calibrating field necessary for building such an organism.
Each cell in our bodies acts like a scalar wave diffraction grating for its genetic information, producing a unique holographic signal which can be read out either audibly through sound waves or electromagnetic radiation; respectively.
Irene Caesar brings an extensive set of lifescience skills, with particular expertise in genomics, bioinformatics, and molecular biology. She earned a Ph.D from Graduate Center CUNY.
