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Program of the 2001 International Worm Meeting - Sternberg Lab ...

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891<br />

891. mab-21 expression is regulated<br />

by genes controlling anes<strong>the</strong>tic<br />

response.<br />

Angus S.K. Leung, K. Wah Chu,<br />

Stephen S.H. Ho, King L. Chow<br />

Department <strong>of</strong> Biology, Hong Kong University<br />

<strong>of</strong> Science and Technology, Clean Water Bay,<br />

Kowloon , HONG KONG.<br />

mab-21 gene encodes a novel protein that<br />

determines cell fate and cell identity in male tail<br />

development. Our previous study in Xenopus<br />

indicated that inhibition <strong>of</strong> frog mab-21<br />

homolog expression resulted in posterior body<br />

patterning defect similar to that in embryos with<br />

FGF signal depleted. This observation promoted<br />

us to examine if mab-21 is acting in <strong>the</strong> FGF<br />

pathway. Using a functional mab-21::gfp fusion<br />

transgene as a reporter, we examine if <strong>the</strong><br />

expression and subcellular localization <strong>of</strong> <strong>the</strong><br />

protein is regulated by worm FGF components,<br />

egl-17 and egl-15. It was noted that mutations in<br />

<strong>the</strong>se genes had no effect on mab-21 expression.<br />

Instead, we observed as enhanced expression <strong>of</strong><br />

mab-21::gfp particularly in <strong>the</strong> hypodermal<br />

tissue in unc-1 mutant, a linked mutation used in<br />

this FGF pathway analysis.<br />

The results suggest that strong expression <strong>of</strong><br />

mab-21::gfp transgene in hypodermis may be<br />

related to <strong>the</strong> functional pathway that controls<br />

sensitivity <strong>of</strong> C. elegans to volatile anaes<strong>the</strong>tic<br />

chemicals. To ascertain such possibility, <strong>the</strong><br />

same reporter transgene was crossed into a<br />

number <strong>of</strong> mutants known to be part <strong>of</strong> this<br />

functional complex. Our result showed that <strong>the</strong><br />

mab-21::gfp expression was up-regulated in<br />

unc-8 and mec-2 mutations, while it was<br />

repressed by unc-24 and unc-79 mutations.<br />

unc-1 encodes stomatin like protein and unc-8<br />

belongs to <strong>the</strong> degenerin family. Both <strong>of</strong> <strong>the</strong>se<br />

genes code for integral membrane proteins,<br />

arguing that MAB-21 expression level and its<br />

function may be regulated by <strong>the</strong> signaling<br />

process downstream <strong>of</strong> <strong>the</strong>se membrane<br />

proteins.<br />

Since <strong>the</strong> reporter was a fusion protein, <strong>the</strong><br />

strong expression may be due to ei<strong>the</strong>r enhanced<br />

transcriptional activity or protein stability.<br />

Experiments are underway to differentiate <strong>the</strong><br />

two possibilities and additional experiments<br />

addressing <strong>the</strong> functional role between <strong>the</strong>se<br />

891<br />

molecules as well as <strong>the</strong> biological significance<br />

<strong>of</strong> such relationship will be presented.

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