Gene Expression

Genetics as it applies to evolution, molecular biology, and medical aspects.

Moderators: Leonid, amiradm, BioTeam

Posts: 345
Joined: Thu Jun 25, 2009 3:15 am

Post by kolean » Sun Jan 31, 2010 12:59 am

JB: interesting argument. First I was not under the impression that we were talking about truncated alleles, or a mutation at all. Also I have a tough time with eukaryotic strong vs. weak promoters in the first place. I think enhancers and the chromatin modeling around each of the alleles is what really makes the alleles stronger than the other one.
You talk about the polypeptide being functional. Do you not need to look at the mRNA first? If the allele with the strong promoter has the mRNA being made into massive quantities, but the truncated form doesn't even get out of the nucleus to be translated into polypeptide (i.e. - no poly(A) site) then it is all for naught as you pointed out. But what if it has been truncated in a way that it can exit the nucleus saftely, but it is not regulated by miRNAs (i.e. - no let-7 miRNA regulatory sites in the 3'UTR), and so the mRNA is translated into massive amounts of polypeptide, while the weak one is regulated heavily due to feed-back loops?
Expression of an allele, in a eukaryote at least, is getting more and more complicated than just using Mendelian's genetic terms of co-dominance, dominance, and recessive. At least for me it is after studying epigenetics, genomic imprinting, and many other maternal influences (maternal miRNAs now? oocytes are getting to be some a heavy developmental influence).
I just have a habit of pointing out that one should not say a word like 'nothing' or especially 'never' (one of my personal pet peeves) when talking about anything in the universe.

User avatar
Inland Taipan
Inland Taipan
Posts: 5694
Joined: Mon Sep 14, 2009 7:12 pm

Post by JackBean » Sun Jan 31, 2010 3:25 pm

by truncated I meant some premature STOP codon, not truncated mRNA ;)

Well, my point was, that there can be but does not have to be a correlation between the strength of promotor and allele dominance. So I used an example taken ad absutio. But still, just take some polypeptide, which has low catalytic speed and other, which is very strong (no matter, which one is original and which mutated;), the first one has stronger promotor, but it catalyze basically nothing, whereas the other one is in the cell only in few copies, but still so strong, that it can override the more-expressed one ;)

The classical examples of dominance and reccessivity are usually based on one gene not working and thus interrupted pathway. In such a case, you can have as strong promotor as you wish, but it will be still reccessive. Or vice versa that can be accomplished by functional allele but non-functional promotor.

Cis or trans? That's what matters.

Post Reply

Who is online

Users browsing this forum: No registered users and 1 guest