Abstract
The expression of two heat-responsive cct (chaperonin-containing Tcp-1) genes from the archaeon Haloferax volcanii was investigated at the transcription level. The cct1 and cct2 genes, which encode proteins of 560 and 557 amino acids, respectively, were identified on cosmid clones of an H. volcanii genomic library and subsequently sequenced. The deduced amino acid sequences of these genes exhibited a high degree of similarity to other archaeal and eucaryal cct family members. Expression of the cct genes was characterized in detail for the purpose of developing a model for studying transcription regulation in the domain Archaea. Northern (RNA) analysis demonstrated that the cct mRNAs were maximally induced after heat shock from 37 to 55 degrees C and showed significant heat inducibility after 30 min at 60 degrees C. Transcription of cct mRNAs was also stimulated in response to dilute salt concentrations. Transcriptional analysis of cct promoter regions coupled to a yeast tRNA reporter gene demonstrated that 5' flanking sequences up to position -233 (cct1) and position -170 (cct2) were sufficient for promoting heat-induced transcription. Transcript analysis indicated that both basal transcription and stress-induced transcription of the H. volcanii cct genes were directed by a conserved archaeal consensus TATA motif (5'-TTTATA-3') centered at -25 relative to the mapped initiation site. Comparison of the cct promoter regions also revealed a striking degree of sequence conservation immediately 5' and 3' of the TATA element.
Full Text
The Full Text of this article is available as a PDF (930.6 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Andrä S., Frey G., Nitsch M., Baumeister W., Stetter K. O. Purification and structural characterization of the thermosome from the hyperthermophilic archaeum Methanopyrus kandleri. FEBS Lett. 1996 Jan 29;379(2):127–131. doi: 10.1016/0014-5793(95)01493-4. [DOI] [PubMed] [Google Scholar]
- Baross J. A., Holden J. F. Overview of hyperthermophiles and their heat-shock proteins. Adv Protein Chem. 1996;48:1–34. doi: 10.1016/s0065-3233(08)60360-5. [DOI] [PubMed] [Google Scholar]
- Charlebois R. L., Lam W. L., Cline S. W., Doolittle W. F. Characterization of pHV2 from Halobacterium volcanii and its use in demonstrating transformation of an archaebacterium. Proc Natl Acad Sci U S A. 1987 Dec;84(23):8530–8534. doi: 10.1073/pnas.84.23.8530. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Charlebois R. L., Schalkwyk L. C., Hofman J. D., Doolittle W. F. Detailed physical map and set of overlapping clones covering the genome of the archaebacterium Haloferax volcanii DS2. J Mol Biol. 1991 Dec 5;222(3):509–524. doi: 10.1016/0022-2836(91)90493-p. [DOI] [PubMed] [Google Scholar]
- Chen X., Sullivan D. S., Huffaker T. C. Two yeast genes with similarity to TCP-1 are required for microtubule and actin function in vivo. Proc Natl Acad Sci U S A. 1994 Sep 13;91(19):9111–9115. doi: 10.1073/pnas.91.19.9111. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chitnis P. R., Nelson N. Molecular cloning of the genes encoding two chaperone proteins of the cyanobacterium Synechocystis sp. PCC 6803. J Biol Chem. 1991 Jan 5;266(1):58–65. [PubMed] [Google Scholar]
- Clarens M., Macario A. J., Conway de Macario E. The archaeal dnaK-dnaJ gene cluster: organization and expression in the methanogen Methanosarcina mazei. J Mol Biol. 1995 Jul 7;250(2):191–201. doi: 10.1006/jmbi.1995.0370. [DOI] [PubMed] [Google Scholar]
- Conway de Macario E., Dugan C. B., Macario A. J. Identification of a grpE heat-shock gene homolog in the archaeon Methanosarcina mazei. J Mol Biol. 1994 Jul 1;240(1):95–101. doi: 10.1006/jmbi.1994.1422. [DOI] [PubMed] [Google Scholar]
- Cowing D. W., Bardwell J. C., Craig E. A., Woolford C., Hendrix R. W., Gross C. A. Consensus sequence for Escherichia coli heat shock gene promoters. Proc Natl Acad Sci U S A. 1985 May;82(9):2679–2683. doi: 10.1073/pnas.82.9.2679. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Creti R., Londei P., Cammarano P. Complete nucleotide sequence of an archaeal (Pyrococcus woesei) gene encoding a homolog of eukaryotic transcription factor IIB (TFIIB). Nucleic Acids Res. 1993 Jun 25;21(12):2942–2942. doi: 10.1093/nar/21.12.2942. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Daniels C. J., McKee A. H., Doolittle W. F. Archaebacterial heat-shock proteins. EMBO J. 1984 Apr;3(4):745–749. doi: 10.1002/j.1460-2075.1984.tb01878.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dear S., Staden R. A sequence assembly and editing program for efficient management of large projects. Nucleic Acids Res. 1991 Jul 25;19(14):3907–3911. doi: 10.1093/nar/19.14.3907. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Frydman J., Nimmesgern E., Erdjument-Bromage H., Wall J. S., Tempst P., Hartl F. U. Function in protein folding of TRiC, a cytosolic ring complex containing TCP-1 and structurally related subunits. EMBO J. 1992 Dec;11(13):4767–4778. doi: 10.1002/j.1460-2075.1992.tb05582.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gupta R. S. Evolution of the chaperonin families (Hsp60, Hsp10 and Tcp-1) of proteins and the origin of eukaryotic cells. Mol Microbiol. 1995 Jan;15(1):1–11. doi: 10.1111/j.1365-2958.1995.tb02216.x. [DOI] [PubMed] [Google Scholar]
- Gupta R. S., Singh B. Cloning of the HSP70 gene from Halobacterium marismortui: relatedness of archaebacterial HSP70 to its eubacterial homologs and a model for the evolution of the HSP70 gene. J Bacteriol. 1992 Jul;174(14):4594–4605. doi: 10.1128/jb.174.14.4594-4605.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hain J., Reiter W. D., Hüdepohl U., Zillig W. Elements of an archaeal promoter defined by mutational analysis. Nucleic Acids Res. 1992 Oct 25;20(20):5423–5428. doi: 10.1093/nar/20.20.5423. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kagawa H. K., Osipiuk J., Maltsev N., Overbeek R., Quaite-Randall E., Joachimiak A., Trent J. D. The 60 kDa heat shock proteins in the hyperthermophilic archaeon Sulfolobus shibatae. J Mol Biol. 1995 Nov 10;253(5):712–725. doi: 10.1006/jmbi.1995.0585. [DOI] [PubMed] [Google Scholar]
- Kagawa Y., Ohta T., Abe Y., Endo H., Yohda M., Kato N., Endo I., Hamamoto T., Ichida M., Hoaki T. Gene of heat shock protein of sulfur-dependent archaeal hyperthermophile Desulfurococcus. Biochem Biophys Res Commun. 1995 Sep 14;214(2):730–736. doi: 10.1006/bbrc.1995.2346. [DOI] [PubMed] [Google Scholar]
- Kaine B. P., Mehr I. J., Woese C. R. The sequence, and its evolutionary implications, of a Thermococcus celer protein associated with transcription. Proc Natl Acad Sci U S A. 1994 Apr 26;91(9):3854–3856. doi: 10.1073/pnas.91.9.3854. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Keeling P. J., Doolittle W. F. Archaea: narrowing the gap between prokaryotes and eukaryotes. Proc Natl Acad Sci U S A. 1995 Jun 20;92(13):5761–5764. doi: 10.1073/pnas.92.13.5761. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kim S., Willison K. R., Horwich A. L. Cystosolic chaperonin subunits have a conserved ATPase domain but diverged polypeptide-binding domains. Trends Biochem Sci. 1994 Dec;19(12):543–548. doi: 10.1016/0968-0004(94)90058-2. [DOI] [PubMed] [Google Scholar]
- Klenk H. P., Palm P., Lottspeich F., Zillig W. Component H of the DNA-dependent RNA polymerases of Archaea is homologous to a subunit shared by the three eucaryal nuclear RNA polymerases. Proc Natl Acad Sci U S A. 1992 Jan 1;89(1):407–410. doi: 10.1073/pnas.89.1.407. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Knapp S., Schmidt-Krey I., Hebert H., Bergman T., Jörnvall H., Ladenstein R. The molecular chaperonin TF55 from the Thermophilic archaeon Sulfolobus solfataricus. A biochemical and structural characterization. J Mol Biol. 1994 Sep 30;242(4):397–407. doi: 10.1006/jmbi.1994.1590. [DOI] [PubMed] [Google Scholar]
- Kubota H., Hynes G., Willison K. The chaperonin containing t-complex polypeptide 1 (TCP-1). Multisubunit machinery assisting in protein folding and assembly in the eukaryotic cytosol. Eur J Biochem. 1995 May 15;230(1):3–16. doi: 10.1111/j.1432-1033.1995.tb20527.x. [DOI] [PubMed] [Google Scholar]
- Lam W. L., Doolittle W. F. Shuttle vectors for the archaebacterium Halobacterium volcanii. Proc Natl Acad Sci U S A. 1989 Jul;86(14):5478–5482. doi: 10.1073/pnas.86.14.5478. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Langer D., Hain J., Thuriaux P., Zillig W. Transcription in archaea: similarity to that in eucarya. Proc Natl Acad Sci U S A. 1995 Jun 20;92(13):5768–5772. doi: 10.1073/pnas.92.13.5768. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Langer D., Zillig W. Putative tfIIs gene of Sulfolobus acidocaldarius encoding an archaeal transcription elongation factor is situated directly downstream of the gene for a small subunit of DNA-dependent RNA polymerase. Nucleic Acids Res. 1993 May 11;21(9):2251–2251. doi: 10.1093/nar/21.9.2251. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lingappa J. R., Martin R. L., Wong M. L., Ganem D., Welch W. J., Lingappa V. R. A eukaryotic cytosolic chaperonin is associated with a high molecular weight intermediate in the assembly of hepatitis B virus capsid, a multimeric particle. J Cell Biol. 1994 Apr;125(1):99–111. doi: 10.1083/jcb.125.1.99. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Macario A. J., Dugan C. B., Conway de Macario E. A dnaK homolog in the archaebacterium Methanosarcina mazei S6. Gene. 1991 Dec 1;108(1):133–137. doi: 10.1016/0378-1119(91)90498-z. [DOI] [PubMed] [Google Scholar]
- Mager W. H., De Kruijff A. J. Stress-induced transcriptional activation. Microbiol Rev. 1995 Sep;59(3):506–531. doi: 10.1128/mr.59.3.506-531.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Marco S., Ureña D., Carrascosa J. L., Waldmann T., Peters J., Hegerl R., Pfeifer G., Sack-Kongehl H., Baumeister W. The molecular chaperone TF55. Assessment of symmetry. FEBS Lett. 1994 Mar 21;341(2-3):152–155. doi: 10.1016/0014-5793(94)80447-8. [DOI] [PubMed] [Google Scholar]
- Marsh T. L., Reich C. I., Whitelock R. B., Olsen G. J. Transcription factor IID in the Archaea: sequences in the Thermococcus celer genome would encode a product closely related to the TATA-binding protein of eukaryotes. Proc Natl Acad Sci U S A. 1994 May 10;91(10):4180–4184. doi: 10.1073/pnas.91.10.4180. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McLennan N. F., Girshovich A. S., Lissin N. M., Charters Y., Masters M. The strongly conserved carboxyl-terminus glycine-methionine motif of the Escherichia coli GroEL chaperonin is dispensable. Mol Microbiol. 1993 Jan;7(1):49–58. doi: 10.1111/j.1365-2958.1993.tb01096.x. [DOI] [PubMed] [Google Scholar]
- Nieuwlandt D. T., Daniels C. J. An expression vector for the archaebacterium Haloferax volcanii. J Bacteriol. 1990 Dec;172(12):7104–7110. doi: 10.1128/jb.172.12.7104-7110.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Palmer J. R., Daniels C. J. A transcriptional reporter for in vivo promoter analysis in the archaeon Haloferax volcanii. Appl Environ Microbiol. 1994 Oct;60(10):3867–3869. doi: 10.1128/aem.60.10.3867-3869.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Palmer J. R., Daniels C. J. In vivo definition of an archaeal promoter. J Bacteriol. 1995 Apr;177(7):1844–1849. doi: 10.1128/jb.177.7.1844-1849.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Palmer J. R., Nieuwlandt D. T., Daniels C. J. Expression of a yeast intron-containing tRNA in the archaeon Haloferax volcanii. J Bacteriol. 1994 Jun;176(12):3820–3823. doi: 10.1128/jb.176.12.3820-3823.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pelham H. R. A regulatory upstream promoter element in the Drosophila hsp 70 heat-shock gene. Cell. 1982 Sep;30(2):517–528. doi: 10.1016/0092-8674(82)90249-5. [DOI] [PubMed] [Google Scholar]
- Perisic O., Xiao H., Lis J. T. Stable binding of Drosophila heat shock factor to head-to-head and tail-to-tail repeats of a conserved 5 bp recognition unit. Cell. 1989 Dec 1;59(5):797–806. doi: 10.1016/0092-8674(89)90603-x. [DOI] [PubMed] [Google Scholar]
- Phipps B. M., Hoffmann A., Stetter K. O., Baumeister W. A novel ATPase complex selectively accumulated upon heat shock is a major cellular component of thermophilic archaebacteria. EMBO J. 1991 Jul;10(7):1711–1722. doi: 10.1002/j.1460-2075.1991.tb07695.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Picketts D. J., Mayanil C. S., Gupta R. S. Molecular cloning of a Chinese hamster mitochondrial protein related to the "chaperonin" family of bacterial and plant proteins. J Biol Chem. 1989 Jul 15;264(20):12001–12008. [PubMed] [Google Scholar]
- Qureshi S. A., Baumann P., Rowlands T., Khoo B., Jackson S. P. Cloning and functional analysis of the TATA binding protein from Sulfolobus shibatae. Nucleic Acids Res. 1995 May 25;23(10):1775–1781. doi: 10.1093/nar/23.10.1775. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Qureshi S. A., Khoo B., Baumann P., Jackson S. P. Molecular cloning of the transcription factor TFIIB homolog from Sulfolobus shibatae. Proc Natl Acad Sci U S A. 1995 Jun 20;92(13):6077–6081. doi: 10.1073/pnas.92.13.6077. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Reiter W. D., Palm P., Zillig W. Analysis of transcription in the archaebacterium Sulfolobus indicates that archaebacterial promoters are homologous to eukaryotic pol II promoters. Nucleic Acids Res. 1988 Jan 11;16(1):1–19. doi: 10.1093/nar/16.1.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rowlands T., Baumann P., Jackson S. P. The TATA-binding protein: a general transcription factor in eukaryotes and archaebacteria. Science. 1994 May 27;264(5163):1326–1329. doi: 10.1126/science.8191287. [DOI] [PubMed] [Google Scholar]
- Sanger F., Nicklen S., Coulson A. R. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463–5467. doi: 10.1073/pnas.74.12.5463. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thomm M., Wich G. An archaebacterial promoter element for stable RNA genes with homology to the TATA box of higher eukaryotes. Nucleic Acids Res. 1988 Jan 11;16(1):151–163. doi: 10.1093/nar/16.1.151. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Trent J. D., Nimmesgern E., Wall J. S., Hartl F. U., Horwich A. L. A molecular chaperone from a thermophilic archaebacterium is related to the eukaryotic protein t-complex polypeptide-1. Nature. 1991 Dec 12;354(6353):490–493. doi: 10.1038/354490a0. [DOI] [PubMed] [Google Scholar]
- Trieselmann B. A., Charlebois R. L. Transcriptionally active regions in the genome of the archaebacterium Haloferax volcanii. J Bacteriol. 1992 Jan;174(1):30–34. doi: 10.1128/jb.174.1.30-34.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vinh D. B., Drubin D. G. A yeast TCP-1-like protein is required for actin function in vivo. Proc Natl Acad Sci U S A. 1994 Sep 13;91(19):9116–9120. doi: 10.1073/pnas.91.19.9116. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vodkin M. H., Williams J. C. A heat shock operon in Coxiella burnetti produces a major antigen homologous to a protein in both mycobacteria and Escherichia coli. J Bacteriol. 1988 Mar;170(3):1227–1234. doi: 10.1128/jb.170.3.1227-1234.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Waldmann T., Lupas A., Kellermann J., Peters J., Baumeister W. Primary structure of the thermosome from Thermoplasma acidophilum. Biol Chem Hoppe Seyler. 1995 Feb;376(2):119–126. doi: 10.1515/bchm3.1995.376.2.119. [DOI] [PubMed] [Google Scholar]
- Waldmann T., Nimmesgern E., Nitsch M., Peters J., Pfeifer G., Müller S., Kellermann J., Engel A., Hartl F. U., Baumeister W. The thermosome of Thermoplasma acidophilum and its relationship to the eukaryotic chaperonin TRiC. Eur J Biochem. 1995 Feb 1;227(3):848–856. doi: 10.1111/j.1432-1033.1995.tb20210.x. [DOI] [PubMed] [Google Scholar]
- Waldmann T., Nitsch M., Klumpp M., Baumeister W. Expression of an archaeal chaperonin in E. coli: formation of homo- (alpha, beta) and hetero-oligomeric (alpha+beta) thermosome complexes. FEBS Lett. 1995 Nov 27;376(1-2):67–73. doi: 10.1016/0014-5793(95)01248-8. [DOI] [PubMed] [Google Scholar]
- Yaffe M. B., Farr G. W., Miklos D., Horwich A. L., Sternlicht M. L., Sternlicht H. TCP1 complex is a molecular chaperone in tubulin biogenesis. Nature. 1992 Jul 16;358(6383):245–248. doi: 10.1038/358245a0. [DOI] [PubMed] [Google Scholar]