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Can Large MPAs Protect Tuna and Sharks?

Thu, 04 Jun 2015 14:04:29 +0000

a guest blog by David Curnick, written for the 2015 Write About Research Competition. With a global human population of over 7 billion it is becoming ever more important to manage our natural resources effectively. For centuries, the oceans have been seen as an endless bounty, ripe for harvesting. However, this simply isn’t the case […]

The post Can Large MPAs Protect Tuna and Sharks? appeared first on GEE Research.

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13 May 2013

"Why does selection care about codon usage (or what really determines ribosome velocity)"


Speaker:

Laurence Hurst
(Bath)
Date & Time:
Wednesday, 22 May at 5pm
Venue: Medical Sciences AV Hill Lecture Theatre (map)
Host: Jurg Bahler (51602)


Abstract
Owing to the structure of the genetic code more than one codon can specify the same amino acid.  At first sight natural selection should not care which of the multiple synonymous codons is employed as the translated protein will be the same regardless.  That we see selection on codon usage is thus intruiging.  Understanding why selection cares about codon usage is important for understanding how cells work and, in turn, for understanding how to intelligently engineer transgenes.  I provide evidence that selection cares about codon usage because it minimizes errors: it ensures translation is accurate and, in mammals, it ensures splicing is accurate. It is also commonly assumed that, because common codons match common tRNAs, codon usage must affect ribosomal velocity. Using ribosome protection data I find no evidence that in normal conditions codon usage has any effect on ribosomal velocity.  In retrospect this result makes sense as the original logic was flawed - it considered only tRNA supply, not codon driven tRNA demand.  We expect evolution to drive towards supply:demand equilibrium at which point rare codons specified by rare tRNAs wait as long to be translated as common codons specified by common tRNAs.  More generally, we see little or no evidence for RNA mediated effects on translational velocity (either codon usage or mRNA structure). This leaves the problem of what does actually determine ribosomal velocity.  I show that positively charged amino acids entering into the negatively charged ribosome exit tunnel have a profound effect on ribosome velocity.   This can explain the evolution of the polyA tail.  Methods to improve transgenes are suggested by these results.

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