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Post by skyship on Jan 24, 2014 18:30:07 GMT -5
HSP60: found in human skin? Gene Symbol: hsp60 Description: heat shock 60kDa protein 1 (chaperonin) Alias: CPN60, GROEL, HLD4, HSP-60, HSP60, HSP65, HuCHA60, SPG13, 60 kDa chaperonin, 60 kDa heat shock protein, mitochondrial, P60 lymphocyte protein, chaperonin 60, heat shock protein 65, mitochondrial matrix protein P1, short heat shock protein 60 Hsp60s1 Species: human www.labome.org/gene/human/hsp60-3329.html========== Phylogenetic analysis of gastric and enterohepatic Helicobacter species based on partial HSP60 gene sequences
... Conclusions In conclusion, we have shown that the 600 bp HSP60 gene sequence is a suitable phylogenetic marker for the genus Helicobacter. The degenerate primers used amplify DNA of several bacterial genera, offering the possibility of extending phylogenetic analysis of diverse bacterial species. New insight into the phylogeny of Helicobacter sp. flexispira taxa was achieved, but further studies are needed to describe the taxonomy of taxa 2 and 3 and taxon 8, H. bilis and canine flexispiras.
The rather high level of interspecies sequence divergence in the genus Helicobacter suggests that development of species-specific PCR or DNA–DNA hybridization tests is also possible for species other than H. salomonis. .... ijs.sgmjournals.org/content/54/3/753.full
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Post by skyship on Jan 26, 2014 16:38:57 GMT -5
Gene Structure Venner et al. (1990) claimed that HSP60 is intronless. Hansen et al. (2003) presented the full sequence of the HSP60 and HSP10 genes. They found that both genes are linked head to head, comprising approximately 17 kb and consisting of 12 and 4 exons, respectively. The first exon of HSP60 is noncoding, and the first exon of HSP10 ends with the start codon. www.omim.org/entry/118190#0002so there is more to this than we know.
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Post by skyship on Jan 26, 2014 16:45:35 GMT -5
Us old timers are finding tiny knobs on ends of these filaments. These are the coding ends that adhere to DNA, thereby making this a DNA issue. Lets look at Venner and Hansen. Remember Hansens Disease? Here is what Venner said: Evidently though, there are 6 pseudogenes(false genes, not human?) in the human genome. Now it was 1987 this took effect, I think. Surmising here, but, this 87 nucleotide is near the 3' end of the shortend DNA, where telomeres could be attached. they say are nonfunctional genes, antisense, anticoding types. My question here is, if these are in the mitochondria genes, that means Mama's genes given to you, passed on to you, making the pseudogene, actually, a hereditary factor. If they are nonfunctional, does the hsp make them functional, thereby producing variation diseases that become DNA diseases. OMIM record these.That would be in Mitochondrial, means altering our given genes, without our knowledge, through the mechanism of heat shock proteins, again ,the sup35p and its affiliation with hsps and "evolutionary capacitance"~!or an "evolutionary conduit"~! Will get into that later.[/b] Now for what Hansen has to say: OMIM is showing this as new disease, it appears. HSP are new to the human genome, or presented as pseudogenes, and I believe Muscular Dystrophy in the past was one of the fallouts from genetic experiments as are the new ones being presented now. The idea is the fallout is the risk, and the new diseases are caused by these new "directed evolutionary projects", so to keep the "create the disease, by stray artefacts, make notes of the consequences, provide the new pharma product, for the new disease" which actually alters your genes, all in the drug. So find the drug, while taking the risk to institute new gene products, the risk: a new disease, then keep the pharma machine oiled~! The new Circle of Life: I prefer the Old One~1, the one we were given; Our native natural progression with no new altered intermediates, causing issues with natural healing, because those cannot be patented, however we know now, they can patent our artefacts~!
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Post by skyship on Jan 26, 2014 17:19:16 GMT -5
Going backwards here, it looks like GroEL and GroEs are subunits of some of these heat shock proteins. They are called "operons".... Remember the "walking dna" from Mendleson? It was made from B.Subtilis. What this informs me, is that this is a genetic operation using HSPs as the catalyst, and I do believe that is what Lindquist has said. A new Phenotype from S. Cerevisciae(Yeast). More on that later as well. Image: Image of phenotype with prions in the ring:
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Post by skyship on Feb 23, 2014 18:05:43 GMT -5
bump up
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