Differential expression of genes influenced by changing salinity using RNA arbitrarily primed PCR in the archaeal halophile Haloferax volcanii

被引:25
作者
Bidle, KA [1 ]
机构
[1] Univ Calif San Diego, Scripps Inst Oceanog, Div Marine Biol Res, La Jolla, CA 92093 USA
关键词
gene expression; Haloferax volcanii; halophile; RAP-PCR; sensor kinase;
D O I
10.1007/s00792-002-0289-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Extreme halophiles belonging to the domain Archaea require a minimum of similar to10% NaCl for growth. Many of these obligate halophiles will continue to grow even as NaCl concentrations approach saturation. The haloarchaeon Haloferax volcanii is a model organism in which to study the effects of changes in medium salinity on gene expression, as this organism grows over a wide range of NaCl concentrations, between 12% and 23%, with little effect on growth rate. An RNA arbitrarily primed PCR (RAP-PCR) approach has been applied to identify those genes that are differentially expressed in response to changing salinity. Differences in gene expression can be detected using this methodology, as each sample generates its own unique RNA fingerprint for each growth condition examined. RNA was prepared from H. volcanii cultures grown with two different NaCl concentrations in the medium, RAP-PCR was performed, and seven differentially expressed transcripts were identified. These fragments were cloned, sequenced, and subjected to transcript analysis to confirm their regulation. One of the sequences identified in this study displays homology to the eukaryotic Ser/Thr protein kinase Ire1p, a sensor of protein unfolding in yeast and mammalian cells: Evidence for serine phosphorylation in H. volcanii is also presented.
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页码:1 / 7
页数:7
相关论文
共 36 条
[1]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[2]   Structural and putative regulatory genes involved in cellulose synthesis in Rhizobium leguminosarum bv. trifolii [J].
Ausmees, N ;
Jonsson, H ;
Höglund, S ;
Ljunggren, H ;
Lindberg, M .
MICROBIOLOGY-UK, 1999, 145 :1253-1262
[3]  
Ausubel FM., 1993, Current Protocols in Molecular Biology
[4]   Analysis of the SOS response in Salmonella enterica serovar Typhimurium using RNA fingerprinting by arbitrarily primed PCR [J].
Benson, NR ;
Wong, RMY ;
McClelland, M .
JOURNAL OF BACTERIOLOGY, 2000, 182 (12) :3490-3497
[5]   RNA arbitrarily primed PCR survey of genes regulated by ToxR in the deep-sea bacterium Photobacterium profundum strain SS9 [J].
Bidle, KA ;
Bartlett, DH .
JOURNAL OF BACTERIOLOGY, 2001, 183 (05) :1688-1693
[6]   Use of RNA arbitrarily primed-PCR fingerprinting to identify Vibrio cholerae genes differentially expressed in the host following infection [J].
Chakrabortty, A ;
Das, S ;
Majumdar, S ;
Mukhopadhyay, K ;
Roychoudhury, S ;
Chaudhuri, K .
INFECTION AND IMMUNITY, 2000, 68 (07) :3878-3887
[7]   SOLUTE CONCENTRATIONS WITHIN CELLS OF HALOPHILIC AND NON-HALOPHILIC BACTERIA [J].
CHRISTIAN, JHB ;
WALTHO, JA .
BIOCHIMICA ET BIOPHYSICA ACTA, 1962, 65 (03) :506-&
[8]   TRANSCRIPTIONAL INDUCTION OF GENES ENCODING ENDOPLASMIC-RETICULUM RESIDENT PROTEINS REQUIRES A TRANSMEMBRANE PROTEIN-KINASE [J].
COX, JS ;
SHAMU, CE ;
WALTER, P .
CELL, 1993, 73 (06) :1197-1206
[9]   ARCHAEBACTERIAL HEAT-SHOCK PROTEINS [J].
DANIELS, CJ ;
MCKEE, AHZ ;
DOOLITTLE, WF .
EMBO JOURNAL, 1984, 3 (04) :745-749
[10]   Evolutionary divergence and salinity-mediated selection in halophilic archaea [J].
Dennis, PP ;
Shimmin, LC .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 1997, 61 (01) :90-&