Archimedes Plut
Reading up about Transposons, I find they exist in *all
cells*. But the transposons I am concerned about are what
*can cause* Alzheimers, Parkinsons and Prion diseases.
If my understanding is correct then these so called "jumping
genes of Transposons" replace the innate genes. So that when
the 20th century researchers were looking for Nucleic Acid
of viruses in connection with prion disease, if the culprit
is a Transposon, well, once it has replaced the innate gene
that sequences for PrP proteins, well, there are just no
Nucleic Acids to be found is there? Unless one looks for the
replaced genes that the Transposon discarded.
So, no wonder researchers seem to fail in finding the
foreign viruslike particle because it was a Transposon. And
now-a-days researchers in prion disease are more involved in
hero worship of Prusiner and the Prusiner Model that no-one
bothers to look for anything other than to bulwark the
Prusiner Model. The field is overrun by hero worshippers
that no scientist has the objectivity to look for
Transposons.
Transposons are viruslike particles but they are
different from the viruses that scientist thought of when
they were looking for viruses to cause Prion disease in
the 20th century.
Yeast is a fungus that has PrP prion proteins and Yeast has
Transposon elements. According to one book source the Ty
transposon elements in yeast involve an RNA intermediate
and that the Ty elements cause mutations. This book
(Genetic Analysis 6th ed) says that Ty elements in yeast
have about 35 copies in the Yeast genome. Now I wonder if
the known Varieties of PrP in human CJD have about 35
*variants*??? So that when we see variant of PrP in one CJD
victim compared to another CJD victim is because the
Transposon replaced one of the 35 spots different from the
other 34 spots on the genome.
So one can appreciate why variants in PrP occur is because
of Transposons.
Archimedes Plutonium www.archimedesplutonium.com
www.iw.net/~a_plutonium whole entire Universe is just one
big atom where dots of the electron-dot-cloud are galaxies
cells*. But the transposons I am concerned about are what
*can cause* Alzheimers, Parkinsons and Prion diseases.
If my understanding is correct then these so called "jumping
genes of Transposons" replace the innate genes. So that when
the 20th century researchers were looking for Nucleic Acid
of viruses in connection with prion disease, if the culprit
is a Transposon, well, once it has replaced the innate gene
that sequences for PrP proteins, well, there are just no
Nucleic Acids to be found is there? Unless one looks for the
replaced genes that the Transposon discarded.
So, no wonder researchers seem to fail in finding the
foreign viruslike particle because it was a Transposon. And
now-a-days researchers in prion disease are more involved in
hero worship of Prusiner and the Prusiner Model that no-one
bothers to look for anything other than to bulwark the
Prusiner Model. The field is overrun by hero worshippers
that no scientist has the objectivity to look for
Transposons.
Transposons are viruslike particles but they are
different from the viruses that scientist thought of when
they were looking for viruses to cause Prion disease in
the 20th century.
Yeast is a fungus that has PrP prion proteins and Yeast has
Transposon elements. According to one book source the Ty
transposon elements in yeast involve an RNA intermediate
and that the Ty elements cause mutations. This book
(Genetic Analysis 6th ed) says that Ty elements in yeast
have about 35 copies in the Yeast genome. Now I wonder if
the known Varieties of PrP in human CJD have about 35
*variants*??? So that when we see variant of PrP in one CJD
victim compared to another CJD victim is because the
Transposon replaced one of the 35 spots different from the
other 34 spots on the genome.
So one can appreciate why variants in PrP occur is because
of Transposons.
Archimedes Plutonium www.archimedesplutonium.com
www.iw.net/~a_plutonium whole entire Universe is just one
big atom where dots of the electron-dot-cloud are galaxies
