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Welcome to the 31st IUBS General Assembly and Conference on ...

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<str<strong>on</strong>g>to</str<strong>on</strong>g> polluti<strong>on</strong> <str<strong>on</strong>g>and</str<strong>on</strong>g> can survive <strong>on</strong>ly in polluti<strong>on</strong> free<br />

envir<strong>on</strong>ments. From <str<strong>on</strong>g>the</str<strong>on</strong>g> presence <str<strong>on</strong>g>the</str<strong>on</strong>g>se species, we can<br />

know <str<strong>on</strong>g>the</str<strong>on</strong>g> water quality of a river.<br />

Natural Selecti<strong>on</strong> in Genome Evoluti<strong>on</strong><br />

Giorgio BERNARDI<br />

Department of Biology, Rome 3 University, Italy. Email:<br />

gbernardi@uniroma3.it<br />

“Most of <str<strong>on</strong>g>the</str<strong>on</strong>g> familiar features of living organisms show<br />

clear signs of adaptati<strong>on</strong> of structure <str<strong>on</strong>g>to</str<strong>on</strong>g> functi<strong>on</strong>. There is<br />

overwhelming evidence that this is <str<strong>on</strong>g>the</str<strong>on</strong>g> outcome of<br />

evoluti<strong>on</strong> by natural selecti<strong>on</strong>” (B Charlesworth). Whe<str<strong>on</strong>g>the</str<strong>on</strong>g>r<br />

<str<strong>on</strong>g>the</str<strong>on</strong>g> same applies <str<strong>on</strong>g>to</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g> genomes of vertebrates (<str<strong>on</strong>g>and</str<strong>on</strong>g><br />

o<str<strong>on</strong>g>the</str<strong>on</strong>g>r eukaryotes) with <str<strong>on</strong>g>the</str<strong>on</strong>g>ir overwhelming amount of<br />

n<strong>on</strong>‐protein‐coding DNA is, however, an open questi<strong>on</strong>.<br />

Many years ago, we developed a compositi<strong>on</strong>al strategy,<br />

which revealed that those genomes are mosaics of<br />

isochores. These are l<strong>on</strong>g DNA stretches fairly<br />

homogeneous in base compositi<strong>on</strong> that bel<strong>on</strong>g <str<strong>on</strong>g>to</str<strong>on</strong>g> a small<br />

number of families characterized by different GC levels<br />

<str<strong>on</strong>g>and</str<strong>on</strong>g> different short‐sequence patterns (i.e.different DNA<br />

structures <str<strong>on</strong>g>and</str<strong>on</strong>g> different DNA‐protein interacti<strong>on</strong>s). This<br />

genome organizati<strong>on</strong> led us <str<strong>on</strong>g>to</str<strong>on</strong>g> 2 discoveries: (i) <str<strong>on</strong>g>the</str<strong>on</strong>g><br />

genomic code, a collective definiti<strong>on</strong> for <str<strong>on</strong>g>the</str<strong>on</strong>g> correlati<strong>on</strong>s<br />

that hold between coding <str<strong>on</strong>g>and</str<strong>on</strong>g> n<strong>on</strong>‐coding sequences;<br />

between coding sequences <str<strong>on</strong>g>and</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g> structural properties<br />

of <str<strong>on</strong>g>the</str<strong>on</strong>g> encoded proteins; <str<strong>on</strong>g>and</str<strong>on</strong>g> between <str<strong>on</strong>g>the</str<strong>on</strong>g> frequencies of<br />

short sequences of isochore families <str<strong>on</strong>g>and</str<strong>on</strong>g> nucleosome<br />

positi<strong>on</strong>ing/transcripti<strong>on</strong> fac<str<strong>on</strong>g>to</str<strong>on</strong>g>r binding. (ii) The genome<br />

phenotypes, which corresp<strong>on</strong>d, at low resoluti<strong>on</strong>, <str<strong>on</strong>g>to</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g><br />

patterns of isochore families in <str<strong>on</strong>g>the</str<strong>on</strong>g> genome; at high<br />

resoluti<strong>on</strong>, <str<strong>on</strong>g>to</str<strong>on</strong>g> isochore maps <strong>on</strong> chromosomes. While <str<strong>on</strong>g>the</str<strong>on</strong>g><br />

latter may be used <str<strong>on</strong>g>to</str<strong>on</strong>g> study genomic variati<strong>on</strong> <str<strong>on</strong>g>and</str<strong>on</strong>g><br />

genomic diseases, <str<strong>on</strong>g>the</str<strong>on</strong>g> former showed that genome<br />

evoluti<strong>on</strong> may proceed according <str<strong>on</strong>g>to</str<strong>on</strong>g> a c<strong>on</strong>servative mode<br />

or <str<strong>on</strong>g>to</str<strong>on</strong>g> a transiti<strong>on</strong>al (shifting) mode. The c<strong>on</strong>servati<strong>on</strong> <str<strong>on</strong>g>and</str<strong>on</strong>g><br />

<str<strong>on</strong>g>the</str<strong>on</strong>g> changes of isochore patterns depend up<strong>on</strong> whe<str<strong>on</strong>g>the</str<strong>on</strong>g>r<br />

<str<strong>on</strong>g>the</str<strong>on</strong>g> envir<strong>on</strong>ment is c<strong>on</strong>stant or shifting. According <str<strong>on</strong>g>to</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g><br />

‘neo‐selecti<strong>on</strong>ist <str<strong>on</strong>g>the</str<strong>on</strong>g>ory’, natural selecti<strong>on</strong> is resp<strong>on</strong>sible<br />

for both modes <str<strong>on</strong>g>and</str<strong>on</strong>g> plays a dominant role in genome<br />

evoluti<strong>on</strong>.<br />

Neutral sphingomyelinase 2 <str<strong>on</strong>g>and</str<strong>on</strong>g> HA<br />

Department of Pediatrics, University of Chicago, Chicago, USA.<br />

Email: qjingd<strong>on</strong>g@peds.bsd.uchicago.edu. This is a recent<br />

study published in JBC.<br />

Fibroblasts from <str<strong>on</strong>g>the</str<strong>on</strong>g> fro/fro mouse, with a deleti<strong>on</strong> in<br />

<str<strong>on</strong>g>the</str<strong>on</strong>g> Smpd3 gene coding for <str<strong>on</strong>g>the</str<strong>on</strong>g> active site of neutral<br />

sphingomyelinase2 (NSMase2), secreted increased<br />

amounts of hyalur<strong>on</strong>an (HA). This was reversed by<br />

transfecti<strong>on</strong> with <str<strong>on</strong>g>the</str<strong>on</strong>g> Smpd3 gene, suggesting a<br />

c<strong>on</strong>necti<strong>on</strong> between sphingolipid <str<strong>on</strong>g>and</str<strong>on</strong>g><br />

glycosaminoglycan metabolism. The deficiency of<br />

NSMase2 resulted in s<str<strong>on</strong>g>to</str<strong>on</strong>g>rage of sphingomyelin (SM)<br />

<str<strong>on</strong>g>and</str<strong>on</strong>g> cholesterol with a 50% reducti<strong>on</strong> in ceramides<br />

(Cer). RT‐PCR <str<strong>on</strong>g>and</str<strong>on</strong>g> Western blot analysis showed that<br />

<str<strong>on</strong>g>the</str<strong>on</strong>g> increased HA secreti<strong>on</strong> resulted from increased<br />

hyalur<strong>on</strong>an synthase 2 (HAS2) activity localized <str<strong>on</strong>g>to</str<strong>on</strong>g><br />

sphingolipid‐enriched lipid rafts. Although cholesterol<br />

levels were also elevated in lipid rafts from mouse<br />

fibroblasts deficient in lysosomal acid SMase activity<br />

(deleti<strong>on</strong> of <str<strong>on</strong>g>the</str<strong>on</strong>g> Smpd1 ‐/‐ gene), <str<strong>on</strong>g>the</str<strong>on</strong>g>re was no increase in<br />

HA secreti<strong>on</strong>. We <str<strong>on</strong>g>the</str<strong>on</strong>g>n showed that in fro/fro fibroblasts,<br />

<str<strong>on</strong>g>the</str<strong>on</strong>g> reduced ceramide was associated with decreased<br />

phosphorylati<strong>on</strong> of protein phosphatase 2A (PP2A) <str<strong>on</strong>g>and</str<strong>on</strong>g><br />

increased phosphorylati<strong>on</strong> of its substrate Akt‐p,<br />

<str<strong>on</strong>g>to</str<strong>on</strong>g>ge<str<strong>on</strong>g>the</str<strong>on</strong>g>r with PI3K, PDK1, mTOR <str<strong>on</strong>g>and</str<strong>on</strong>g> p‐70S6K whereas<br />

PTEN was unaffected. Exogenous ceramide, as well as<br />

inhibi<str<strong>on</strong>g>to</str<strong>on</strong>g>rs of Akt (Akt inhibi<str<strong>on</strong>g>to</str<strong>on</strong>g>r VIII), PI3kinase<br />

(LY294002 <str<strong>on</strong>g>and</str<strong>on</strong>g> wortmannin) <str<strong>on</strong>g>and</str<strong>on</strong>g> mTOR (rapamycin)<br />

reduced secreti<strong>on</strong> of HA whereas <str<strong>on</strong>g>the</str<strong>on</strong>g> NSMase2<br />

inhibi<str<strong>on</strong>g>to</str<strong>on</strong>g>r GW4869 increased HA syn<str<strong>on</strong>g>the</str<strong>on</strong>g>sis <str<strong>on</strong>g>and</str<strong>on</strong>g><br />

secreti<strong>on</strong>. We propose that NSMase2/Cer are <str<strong>on</strong>g>the</str<strong>on</strong>g> key<br />

media<str<strong>on</strong>g>to</str<strong>on</strong>g>rs of <str<strong>on</strong>g>the</str<strong>on</strong>g> regulati<strong>on</strong> of HA syn<str<strong>on</strong>g>the</str<strong>on</strong>g>sis, via<br />

microdomains <str<strong>on</strong>g>and</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g> Akt /mTOR pathway.<br />

New au<str<strong>on</strong>g>to</str<strong>on</strong>g>matic methods for detecting<br />

quarantine pests <str<strong>on</strong>g>and</str<strong>on</strong>g> diseases<br />

M FACCOLI, F CHINELLATO, E PETRUCCO<br />

TOFFOLO, M SIMONATO <str<strong>on</strong>g>and</str<strong>on</strong>g> A BATTISTI<br />

Department of Agr<strong>on</strong>omy, Food, Natural Resources, Animals<br />

<str<strong>on</strong>g>and</str<strong>on</strong>g> Envir<strong>on</strong>ment, Università di Padova, Italy <str<strong>on</strong>g>and</str<strong>on</strong>g> Agripolis,<br />

Viale dell'Università, 16–35020 Legnaro (PD), Italy. Email:<br />

massimo.faccoli@unipd.it<br />

Jingd<strong>on</strong>g QIN<br />

68

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