
Ask Biotech Questions!
#121
Posted 10 April 2006 - 05:00 PM
#122
Posted 10 April 2006 - 05:18 PM

#123
Posted 12 May 2006 - 06:45 PM
#124
Posted 13 May 2006 - 02:35 PM
Having seen that happen in High School biology classes, I've always suspected that cremation is not actually painless. Corpses sit up in fires and are ritually beaten down by relatives (in India) until their skulls explode.
Likewise, perhaps being cryonically suspended involves some sort of sensatory stimulation and/or awareness since the body's entire nervous system remains intact.
#125
Posted 13 May 2006 - 05:11 PM
How do organisms with no brain exibit stimulus-and-responce behaviour?
hhhm, do you mean "running like a chicken with its head cut off"? I'll let a real scientist go for a more nuanced response, but common sense would dictate that certain aspects of coordination and reflexive response are/can be stored in areas of the central nervous system outside of the brain. This would make sense both in terms of optimizing response time and distributing work load.
I'm not sure if this is germane, but my favorite childhood plant, the Venus Flytrap also comes to mind.
#126
Posted 14 May 2006 - 02:35 AM
I think the Venus Flytrap example is more akin to the twitching of a frog's leg. Doesn't it automatically close even when it is your finger touching it?
#127
Posted 14 May 2006 - 03:01 AM
common sense would dictate that certain aspects of coordination and reflexive response are/can be stored in areas of the central nervous system outside of the brain
On the money.
#128
Posted 14 May 2006 - 06:35 AM
common sense would dictate that certain aspects of coordination and reflexive response are/can be stored in areas of the central nervous system outside of the brain
and indeed they do. Try to consciously inhibit the patella reflex. You can't. Unless you tighten your hamstrings before the hammer hits
#129
Posted 14 May 2006 - 09:23 AM
Having seen that happen in High School biology classes, I've always suspected that cremation is not actually painless. Corpses sit up in fires and are ritually beaten down by relatives (in India) until their skulls explode.
Likewise, perhaps being cryonically suspended involves some sort of sensatory stimulation and/or awareness since the body's entire nervous system remains intact.
*screams in terror*
I don't think this would apply in cryonics, as allthough the CNS is intact it's kinda frozen and not doing anything.
#130
Posted 14 May 2006 - 05:10 PM
#131
Posted 14 May 2006 - 10:59 PM
Ok, thanks for the responses, but I didn't phrase the question quite right. I meant how does an organism with no central nervious system at all exhibit stimulus-and-response behavior. I'm thinking more of single celled organisms (especially preaditors), but it also applied to plants I suppose.
I had a feeling you were going for something different. As per my venus flytrap example, a CNS is not necessary for a cybernetic system to exist.
Cybernetics = The theoretical study of communication and control processes in biological, mechanical, and electronic systems, especially the comparison of these processes in biological and artificial systems.
These links may also be helpful:
en.wikipedia.org/wiki/Cybernetics
en.wikipedia.org/wiki/Feedback
and if mathematics is more to your taste...
en.wikipedia.org/wiki/Control_theory
#132
Posted 15 May 2006 - 06:09 PM
Having seen that happen in High School biology classes, I've always suspected that cremation is not actually painless. Corpses sit up in fires and are ritually beaten down by relatives (in India) until their skulls explode.
It is painless, because they've already died. The "sitting up" motion is purely a mechanical response. It is not an electrochemically-modulated reflex as in a healthy nervous system. The frog response exists because (presumably) the nerve cells have not shriveled up and died yet.
#133
Posted 23 May 2006 - 08:51 AM
2. Regardless of the pairs ("Adenine and Thymine" or "Guanine and Cytosine"); A particular pair can be associated to one precise instruction or perhaps it, the pair, is responsible for more than one instructions? Same question below, attempting to phrase better. A pair of one Adenine molecule and one Thymine molecule located at any given point on the chromosome; does it have multiple functions/instructions/characteristics?
#134
Posted 31 May 2006 - 05:52 AM
#135
Posted 31 May 2006 - 11:08 PM
1. Do each of the Deoxyribonucleic Acid bases (Adenine, Thymine, Guanine, Cytosine) have the ability to give instructions by themselves without pairing up with their counterpart/equal?
2. Regardless of the pairs ("Adenine and Thymine" or "Guanine and Cytosine"); A particular pair can be associated to one precise instruction or perhaps it, the pair, is responsible for more than one instructions? Same question below, attempting to phrase better. A pair of one Adenine molecule and one Thymine molecule located at any given point on the chromosome; does it have multiple functions/instructions/characteristics?
I'll try to answer your question as best I understand it. First of all it's important to realize that only one strand is transcribed into mRNA, this is called the template strand and it forms complementary base pairs with the mRNA. The mRNA itself is single stranded. Each base pair by itself, however, is meaningless. Three base pairs are actually needed to code for each amino acid. Three base pairs together is called a codon. So when you speak of instructions you must realize that they are only given in codons, or triplets. An easy answer to your first question however is that there are single stranded DNA viruses.
Regarding your second question, there are many genes that overlap, meaning that some of the base pairs in a gene also encode an adjacent gene. Do a search for overlapping genes and you'll get lots of info. Also there may be a gene on one strand and another gene on the other strand, both coding for different proteins but each serving as the non-template strand for the other. Hope this helps.
#136
Posted 01 June 2006 - 12:23 AM
A single base pair change alters a codon sequence and can change the amino acid the codon encodes for. When the mRNA is translated into an amino acid sequence this can result in a protein with altered properties (or when the mRNA is used to silence genes, in altered regulation of gene expression; and many other effects based on where the base is located). When the human genome was sequenced, millions of single base changes were found to be located at specific regions in the genome. They are called single nucleotide polymorphisms (SNPs) and they have been found to be important molecular signposts that aid in identifying altered gene function.Each base pair by itself, however, is meaningless.
#138
Posted 01 June 2006 - 06:41 AM
Why do senescent cells secrete factors that can promote tissue damage, including the malignant transformation of neighboring cells? (e.g. here)
You mean as in, is there a selective advantage for it?
There is a phenomenon known as the "bystander effect" where a damaged cell can signal surrounding cells to become apoptotic. This has been widely described in radiation-induced cell damage. It could be a fast-track strategy to cull cells that may be damaged due to their proximity.
#139
Posted 01 June 2006 - 08:17 AM
Yes, selective advantage, selection of something else that causes it, or basically anything that could help with rationalizing the phenomenon...?
#140
Posted 01 June 2006 - 08:57 AM
But Campisi there did not report killing, but rather making them malignant.
Malignancy is another word for proliferation which is associated with growth factors. If, for example, the senescent cell were secreting growth factors it could be a compensatory strategy but one that has carcinogenic consequences under the wrong circumstances. It all depends on what the secreted factors are and in Campisi's article their identity is not discussed or speculated on. It may be that this sort of thing is occuring all the time - when certain cells reach senescence they signal other cells around them to proliferate because they themselves cannot any longer - but in the aged context when cells are increasingly losing regulatory controls then the normally beneficial growth signals become carcinogenic.
#141
Posted 01 June 2006 - 04:21 PM
So if you are right, and the old explanation of senescence is wrong, then the question would become why does senescence exist in the first place, and why don't the damaged cells just apoptose and let normal healing mechanisms take care of it?
#142
Posted 12 June 2006 - 08:48 PM
It seems that looking for genes that affect aging from a bottom up approach is one method being pursued. Why not generate an assay for a various cell types on a periodic basis over the lifetime of different species and then evaluate the genes being expressed at the different ages? It seems that large samplings across species and within species would identify the guilty parties. From there work downstream on the proteomics to find the pathways that are being disrupted by the varied gene expression later in life and focus on drug therapies for those. Are there limiting factors to this approach?
#143
Posted 18 June 2006 - 02:25 AM
#144
Posted 18 June 2006 - 12:32 PM
As one ages the affects of this cycle increases exponentially which is fairly consistent with the data. Would restoring some level of an elderly person's gene expression to that of a young person have a significant impact on longevity? Regarless which of the various theories of aging are correct it would seem the research emphasis on fixing the physiological damage that is structurally inhibiting proper expression and then finding the genes that modulate aging gene expression and then finding ways to regulate them would be the highest priorities. I'm just thinking aloud here so I'm probably just coming to the same conclusions that others who have been studying this stuff for awhile.
1. GEIGL, J.B., S. LANGER, S. BARWISCH, et al. 2004. Analysis of gene expression
patterns and chromosomal changes associated with aging. Cancer Res. 64: 8550–
8557.
#145
Posted 23 June 2006 - 05:17 PM
Is there (existing or in development) virtual and or biological dna synthesizers?
#146
Posted 05 July 2006 - 05:25 PM
I ask in reguards to possible life extension and systems repair, not cosmetic.
#147
Posted 30 July 2006 - 10:30 AM
There is only one de-novo procedure in industrial use, which is the phosphoamitide chemistry. If you want to synthesize DNA, the way to go is most likely to outsource it. You get custom gene synthesis at about $1 per base pair. "Biological" synthesizers (pcr, cloning) are much cheaper, faster and better, but more or less confined to replicate pre-existing sequences. Not sure what you mean by virtual.What are the different types of DNA synthesizers?
#148
Posted 30 July 2006 - 10:33 AM
I had almost forgot about this question. By virtual I meant like a virtual PC. Ie you get some idea of how a dna synthesizer would work by using a simulated one on your PC.
#149
Posted 02 August 2006 - 04:19 PM
#150
Posted 25 August 2006 - 05:58 PM
Edited by maestro949, 25 August 2006 - 10:00 PM.
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