Dak Posted March 7, 2005 Posted March 7, 2005 hi everyone am currently wrighting my bacholorate dissertation, and was wondering if i could pick your brains on a subject? basiccally, i was wondering if anyone knows whether the prokaryotic genes encoding restriction enzymes will be properly expressed by eukaryotes, in particular humans i cannot find any published data on this subject, so if anyone has any idea -- anecdotal or otherwize -- i would very much appreciate it thanx all
Bluenoise Posted March 13, 2005 Posted March 13, 2005 Just a running thought here. Well microbes that produce REN's have thier REN sites methylated to protect themselves right? So wouldn't producing functional REN's in eukaryotes lacking these protection cut-up thier own DNA? Assuming the REN is capable of moving accross the nuclear membrane. There should be no reason why the ORF cannot be properly transcribed and translated. I guess It boils down to 1) if the protein produced will be functional (my guess yes). 2) What interaction said REN if functional will have with a eukaryotic cell. I think this second question is where the problem lies that either the cell will actively degrade the REN or that the REN will degrade your hosts DNA. So you'd either get no RENS, or a cell that dies once properly modified.
rakuenso Posted March 13, 2005 Posted March 13, 2005 hi everyone am currently wrighting my bacholorate dissertation' date=' and was wondering if i could pick your brains on a subject? basiccally, i was wondering if anyone knows whether the prokaryotic genes encoding restriction enzymes will be properly expressed by eukaryotes, in particular humans i cannot find any published data on this subject, so if anyone has any idea -- anecdotal or otherwize -- i would very much appreciate it thanx all[/quote'] Even if it was possible, I'm not sure exactly as how you can express it feasibly since it would require you to directly insert it into the gametes
Skye Posted March 13, 2005 Posted March 13, 2005 But that's quite possible, a good description: http://users.rcn.com/jkimball.ma.ultranet/BiologyPages/T/TransgenicAnimals.html
rakuenso Posted March 13, 2005 Posted March 13, 2005 Even if it was technically possible, crazy right wings and religious groups wouldnt allow it for the heck of it. But interesting read...
Dak Posted March 16, 2005 Author Posted March 16, 2005 hi there, cheers all for your replys the idea that im investigating in my dissertation is the potential use(s) of restriction enzymes to combat hiv infection, so to answre the issues that you rased: the gene would not be inserted into the gamete, but into the genome of the cd4+ cells (helper-T-cells, macrophages, dendrites) using a HIV vector the host genome would be protected from restriction by either: using a restriction enzyme that cannot re-enter the nucleus after being trannslated (which could restrict the HIV genes as they travel through the cytoplasm); using a restriction enzyme that is regulated by a HIV-tat promotor, ie upon hiv infection would create a restriction enzyme to completely distroy the cell; or introdusing both the restriction enzyme gene and the methylation enzyme gene aswell, There should be no reason why the ORF cannot be properly transcribed and translated. I guess It boils down to1) if the protein produced will be functional (my guess yes). 2) What interaction said REN if functional will have with a eukaryotic cell. I think this second question is where the problem lies that either the cell will actively degrade the REN or that the REN will degrade your hosts DNA. So you'd either get no RENS, or a cell that dies once properly modified. if it would be translated, then does anyone know whether or not the cell would degrade the res enzm? i cant find any published info on this anywhere (unsurprisingly). and what does ORF mean? cheers again for all your replys
Dak Posted March 16, 2005 Author Posted March 16, 2005 oh right, open reading frame. makes scence now
Bluenoise Posted March 16, 2005 Posted March 16, 2005 I think the main question you should ask is why do Eukaryotes not have restriction enzymes in the first place? They seem like a very valuable defense so there might be a good reason behind their absense. I'll ask molecular biology proff of mine and see what she has to say. Here's something you should think of. HIV is a retero virus, so it doesn't contain DNA. If the reverse transcription happens in a manner where the DNA might get into the nucleus before the REN can get to it then you might need a REN that has to be able to access the neucleus to remove it. Which would also require methylase activity to protect the host. hmm
Dak Posted March 16, 2005 Author Posted March 16, 2005 "hmm" indeed... alot of annoying hurdles to sort out in this idea hiv reverse-transcribes in the cytoplasm before transporting a DNA copy of its genome into the nucleus, so cytoplasmic ResNms could cut it up in the cytoplasm and leave the host genome intact, as long as the ResNms do not gain entry into the nucleus. i believe that eukaryotes probably ditched the bacterial Res-Mod system as we use methylations for other purposes -- cytosine methylation is used to deactivate genes and adenosine methylation performs an unknown function in eukaryotes, but it is thought to maybe be involved in binding long loops of dna to the nuclear membrane during dna synthesis (any imput on the role of A methylation would be appreciated), and C and A are the only two bases that can be methylased. i guess gene regulation is a more important function than cellular immunity, as we already have an immune system to protect us, and methylations cannot easaly perform both functions simultaniously.
Bluenoise Posted March 16, 2005 Posted March 16, 2005 If the reason we don't have restriction enzymes is because methylation is reserved for higher purposes, then it'd make sense that RENs are able to enter the nuclues. If they couldn't methylation wouldn't matter either way. So either evolution didn't create REN's that are not able to acess Eukaryotic DNA, or having REN'S not active towards the Host's Chromosome lowers their usefullness to the point where they wouldn't be maintained in an Eukaryotic population. If they can't cut out of the nucleus, some viral DNA might still slip by and infect it at which point it'd be safe from restriction enzymes. Maybe the metabolic load of maintaining enough REN to be usefull might also be too high, we have other imune defenses already. Yeah lots of questions.
nahid Posted April 27, 2006 Posted April 27, 2006 hi everyone am currently wrighting my bacholorate dissertation' date=' and was wondering if i could pick your brains on a subject? basiccally, i was wondering if anyone knows whether the prokaryotic genes encoding restriction enzymes will be properly expressed by eukaryotes, in particular humans i cannot find any published data on this subject, so if anyone has any idea -- anecdotal or otherwize -- i would very much appreciate it thanx all[/quote'] Hi, I have valuable information about your idea.PLZ give me your email adress. sincerely
mattbimbo Posted April 27, 2006 Posted April 27, 2006 hi dak, you may find it interesting to consider RNAinterference. and VDJ recombination.
Dak Posted April 27, 2006 Author Posted April 27, 2006 Weee, it's my first ever post Thanks guys, but I've handed my dissertation in now.
Nashyboyo Posted April 30, 2006 Posted April 30, 2006 Just out of interest Which restriction enzyme was it ? Why do you want to put it into a eukaryotic cell ? There are restriction enzyme properties in many proteins present in the eukaryotic nucleus!
Dak Posted April 30, 2006 Author Posted April 30, 2006 it was for my dissertation, disscussing the possible anti-viral uses of restrictases.
BioWizard Posted May 2, 2006 Posted May 2, 2006 For your purposes, you might be interested to look into interfering RNA (RNAi) instead of restriction enzymes, which as everyone has pointed out, might be a bit troublesome.
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