LOCALIZATION OF HISTONE-LIKE PROTEINS IN THERMOPHILIC ARCHAEA BY IMMUNOGOLD ELECTRON-MICROSCOPY

被引:25
作者
BOHRMANN, B
KELLENBERGER, E
ARNOLDSCHULZGAHMEN, B
SREENIVAS, K
SURYANARAYANA, T
STROUP, D
REEVE, JN
机构
[1] UNIV BASEL,BIOZENTRUM,DEPT MICROBIOL,CH-4056 BASEL,SWITZERLAND
[2] UNIV DORTMUND,INST ARBEITSPHYSIOL,D-44139 DORTMUND,GERMANY
[3] UNIV HYDERABAD,DEPT BIOCHEM,HYDERABAD 500134,ANDHRA PRADESH,INDIA
[4] OHIO STATE UNIV,DEPT MICROBIOL,COLUMBUS,OH 43210
关键词
D O I
10.1006/jsbi.1994.1008
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
Immunogold staining combined with heavy metal-based DNA immunostaining of ultrathin sections of cryofixed, freeze-substituted, and resin-embedded cells has revealed that in the hyperthermophilic archaeon, Sulfolobus acidocaldarius, the histone-like proteins HSNP-A and HSNP-C' are colocalized with DNA in the ribosome-free nucleoid, whereas DBNP-B is located exclusively in the ribosome-containing cytoplasm. Following chemical fixation and solvent dehydration the chromatin was resistant to aggregation, indicative of a high protein content. Immunogold labeling of chromatin released from isolated nucleoids of S. acidocaldarius demonstrated that the helix-stabilizing protein HSNP-C' was randomly distributed on both filamentous DNA and on more globular material present within distinct nucleoid subdomains. DNA-dependent RNA polymerase molecules were located by immunogold staining predominantly in the cytoplasmic region immediately surrounding the nucleoid in S. acidocaldarius, presumably at the locations of active transcription. Affinity-purified antibodies raised against HMf, a histone-like protein isolated from the hyperthermophilic and only distantly related methanogenic archaeon Methanothermus fervidus, were also found to be localized almost exclusively to the DNA-containing, ribosome-free nucleoid region. (C) 1994 Academic Press, Inc.
引用
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页码:70 / 78
页数:9
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