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The protease genes expression in Ulva fasciata (Ulvales, Chlorophyta) in relation to hypersalinity-induced oxidative stress and protein oxidation

This study has investigated the gene expression of ubiquitin¡B20S proteasome beta subunit type 1 (20s£]1)¡Bubiquitin-conjugating enzyme e2 (ucee2)¡BATP-dependent caseinolytic protease regulatory subunit (clpC) in the marine macroalga Ulva fasciata Delile in relation to the hypersalinity-induced oxidative stress and protein oxidation. During the early stage (0-1 h), the water contents and TTC (2,3,5-tripheny tetrazolium chloride) reduction ability maintained unchanged but recovery ability and photosynthetic ability (PS II activity as indicated by Fv/Fm) were decreased along with accumulated H2O2, suggesting the occurrence of oxidative stress. Only ubiquitin expressed at this stage. During 1-3 h, water lost (approximately 33% of the control) with a further decrease in recovery ability, TTC reduction ability¡BPS II activity but more H2O2 accumulation and protein carbonyl compound. The transcripts of 20s£]1 and clpC and caseinolytic protease activity increased at this stage with the maximum of clpC at hour 3. In the 6-48 h, water lost seriously with high accumulated free amino acid at 6-12 h but low recovery ability. The transcript amounts of ubiquitin¡B20s£]1 and ucee2 increased marked during this stage, in which these might be related to programmed cell death caused by long-term exposure to hypersalinity. Reactive oxygen species (ROS) scavengers inhibited H2O2 accumulation, caseinolytic proteolytic activity increase, carbonyl compound formation and gene expression of ubiquitin¡B20s£]1¡Bucee2¡BclpC, indicating a role of ROS in the regulation of protease genes. A role of polyamines in the regulation of protease gene expression was tested. Spermidine and spermine inhibited the gene expression of ubiquitin¡B20s£]1 and ucee2, the oxidation of proteins (carbonyl groups) and the induction of caseinolytic protease activity in 90‰-treated thalli, whereas putrescine inhibited clpC expression, the oxidation of proteins and caseinolytic protease activity but enhanced the gene expression of ubiquitin¡B20s£]1 and ucee2. In conclusion, the results of the present investigation show that the degradation of oxidatively damaged proteins under hypersalinity conditions by increased caseinolytic protease activity is driven by the up-regulation of clpC gene expression via ROS and polyamines. It seems likely that the induction of ubiquitin¡B20s£]1 and ucee2 gene expression might be associated with the hypersalinity-mediated programmed cell death.

Identiferoai:union.ndltd.org:NSYSU/oai:NSYSU:etd-0718106-000701
Date18 July 2006
CreatorsSung, Ming-Hsuan
ContributorsMing-Tsair Chan, Tse-Min Lee, Yaw-Huei Lin
PublisherNSYSU
Source SetsNSYSU Electronic Thesis and Dissertation Archive
LanguageCholon
Detected LanguageEnglish
Typetext
Formatapplication/pdf
Sourcehttp://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0718106-000701
Rightscampus_withheld, Copyright information available at source archive

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