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

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improve its website <str<strong>on</strong>g>and</str<strong>on</strong>g> database quality which will<br />

fur<str<strong>on</strong>g>the</str<strong>on</strong>g>r promote idea exchanges <str<strong>on</strong>g>and</str<strong>on</strong>g> accurate modeling<br />

studies. BCGC will also improve public awareness about<br />

its research output, which may help in <str<strong>on</strong>g>the</str<strong>on</strong>g> policy‐making<br />

of governments for managing our biological resources.<br />

Bio<strong>on</strong>Group<br />

Bio<strong>on</strong>Group was established in<br />

2001. Now it has become <str<strong>on</strong>g>the</str<strong>on</strong>g><br />

first Chinese media platform <str<strong>on</strong>g>and</str<strong>on</strong>g> professi<strong>on</strong>al service<br />

provider of biological medicine industry. Relying <strong>on</strong> <str<strong>on</strong>g>the</str<strong>on</strong>g><br />

Internet, Bio<strong>on</strong>Group can provide c<strong>on</strong>sulting research,<br />

industry analysis, br<str<strong>on</strong>g>and</str<strong>on</strong>g> packaging, product promoti<strong>on</strong>,<br />

human resources, c<strong>on</strong>ference planning <str<strong>on</strong>g>and</str<strong>on</strong>g><br />

comprehensive service system for enterprises,<br />

research <str<strong>on</strong>g>and</str<strong>on</strong>g> development instituti<strong>on</strong>s, universities,<br />

parks <str<strong>on</strong>g>and</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g> government of biological medicine<br />

industry. Bio<strong>on</strong>Group c<strong>on</strong>tains six websites (for<br />

example: www.bio<strong>on</strong>.com, www.bio<strong>on</strong>.com.cn,<br />

www.pharm<strong>on</strong>.com.cn,<br />

www.bio<strong>on</strong>job.com,<br />

www.bioinsight.com.cn, <str<strong>on</strong>g>and</str<strong>on</strong>g> www.bioevent.cn) <str<strong>on</strong>g>and</str<strong>on</strong>g><br />

core database of biological medicine industry, so we<br />

can provide <str<strong>on</strong>g>the</str<strong>on</strong>g> leading, accurate, efficient service<br />

systems <str<strong>on</strong>g>and</str<strong>on</strong>g> soluti<strong>on</strong>s.<br />

Ceramide regulati<strong>on</strong> of HA synthase<br />

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

University of Chicago, Rm C‐418, 5841 S Maryl<str<strong>on</strong>g>and</str<strong>on</strong>g> Ave, MC<br />

4068, USA. Email: qjingd<strong>on</strong>g@peds.bsd.uchicago.edu<br />

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

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> glycosaminoglycan<br />

metabolism. The deficiency of NSMase2 resulted in<br />

s<str<strong>on</strong>g>to</str<strong>on</strong>g>rage of sphingomyelin (SM) <str<strong>on</strong>g>and</str<strong>on</strong>g> cholesterol with a<br />

50% reducti<strong>on</strong> in ceramides (Cer). RT‐PCR <str<strong>on</strong>g>and</str<strong>on</strong>g> Western<br />

blot analysis showed that <str<strong>on</strong>g>the</str<strong>on</strong>g> increased HA secreti<strong>on</strong><br />

resulted from increased hyalur<strong>on</strong>an synthase 2 (HAS2)<br />

activity localized <str<strong>on</strong>g>to</str<strong>on</strong>g> sphingolipid‐enriched lipid rafts.<br />

Although cholesterol levels were also elevated in lipid rafts<br />

from mouse fibroblasts deficient in lysosomal acid SMase<br />

activity (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<br />

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

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

decreased phosphorylati<strong>on</strong> of protein phosphatase 2A<br />

(PP2A) <str<strong>on</strong>g>and</str<strong>on</strong>g> increased phosphorylati<strong>on</strong> of its substrate<br />

Akt‐p, <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<br />

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

well as 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 inhibi<str<strong>on</strong>g>to</str<strong>on</strong>g>r<br />

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> secreti<strong>on</strong>. We<br />

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

regulati<strong>on</strong> of HA syn<str<strong>on</strong>g>the</str<strong>on</strong>g>sis, via microdomains <str<strong>on</strong>g>and</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g><br />

Akt/mTOR pathway.<br />

Characterizati<strong>on</strong> <str<strong>on</strong>g>and</str<strong>on</strong>g> functi<strong>on</strong>al<br />

identificati<strong>on</strong> of vacuolar Na + /H + antiporter<br />

from Nitraria sibirica Pall<br />

Li WANG 1 ,Xiaofei LIN 1 , Huiping MAO 1<br />

<str<strong>on</strong>g>and</str<strong>on</strong>g>Wenbo ZHANG 2<br />

1College of Life Sciences, Inner M<strong>on</strong>golia University, Hohhot<br />

010021, China <str<strong>on</strong>g>and</str<strong>on</strong>g> 2College of Forestry, Inner M<strong>on</strong>golia<br />

Agricultural University, Hohhot 010019, China. Email:<br />

linxiaofei04@hotmail.com<br />

Vacuolar Na + /H + antiporters play an important role in<br />

plants salt <str<strong>on</strong>g>to</str<strong>on</strong>g>lerance, which can deliver Na + in<str<strong>on</strong>g>to</str<strong>on</strong>g> <str<strong>on</strong>g>the</str<strong>on</strong>g><br />

vacuoles against <str<strong>on</strong>g>the</str<strong>on</strong>g> electrochemical gradient. The<br />

compartmentati<strong>on</strong> of Na + provides an effective<br />

mechanism <str<strong>on</strong>g>to</str<strong>on</strong>g> avert <str<strong>on</strong>g>the</str<strong>on</strong>g> deleterious effects of Na + <strong>on</strong><br />

cy<str<strong>on</strong>g>to</str<strong>on</strong>g>sol, <str<strong>on</strong>g>and</str<strong>on</strong>g> maintain an osmotic potential by Na + in <str<strong>on</strong>g>the</str<strong>on</strong>g><br />

vacuoles. In this study, using <str<strong>on</strong>g>the</str<strong>on</strong>g> method of degenerate<br />

PCR <str<strong>on</strong>g>and</str<strong>on</strong>g> rapid amplificati<strong>on</strong> of cDNA ends (RACE), an<br />

ortholog of Na + /H + antiporter, referred <str<strong>on</strong>g>to</str<strong>on</strong>g> as NsNHX1,<br />

was isolated from Nitraria sibirica Pall.<br />

The cl<strong>on</strong>ed NsNHX1 cDNA c<strong>on</strong>tains 2182‐bp, with a<br />

predicted ORF of 1635‐bp. The predicted NsNHX1 ORF<br />

encodes a protein of 544 amino acids with 59.9 kDa of<br />

<str<strong>on</strong>g>the</str<strong>on</strong>g>oretical molecular mass <str<strong>on</strong>g>and</str<strong>on</strong>g> 8.15 of isoelectric point.<br />

The predicted amino acid sequence has an<br />

amiloride‐binding motif <str<strong>on</strong>g>and</str<strong>on</strong>g> c<strong>on</strong>served domains as kefB,<br />

CPA2, b‐cpa1, NhaP, etc. The phylogenetic analysis shows<br />

that NsNHX1 forms a clade with <str<strong>on</strong>g>the</str<strong>on</strong>g> most closely related<br />

plant NHX homologs, which was distinct from <str<strong>on</strong>g>the</str<strong>on</strong>g> cluster<br />

of plasma membrane Na + /H + antiporters such as AtSOS1,<br />

97

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