The Fis protein: it's not just for DNA inversion anymore

Higher-order nucleoprotein complexes are associated with many biological processes. In bacteria the formation of these macromolecular structures for DNA recombination, replication, and transcription often requires not only the participation of specific enzymes and co-factors, but also a class of DNA-binding proteins collectively known as 'nucleoid-associated' or 'histone-like' proteins. Examples of this class of proteins are HU, Integration Host Factor, H-NS, and Fis. Fis was originally identified as the factor for inversion stimulation of the homologous Hin and Gin site-specific DNA recombinases of Salmonella and phage Mu, respectively. This small, basic, DNA-bending protein has recently been shown to function in many other reactions including phage lambda site-specific recombination, transcriptional activation of rRNA and tRNA operons, repression of its own synthesis, and oriC-directed DNA replication. Cellular concentrations of Fis vary tremendously under different growth conditions which may have important regulatory implications for the physiological role of Fis in these different reactions. The X-ray crystal structure of Fis has been determined and insights into its mode of DNA binding and mechanisms of action in these disparate systems are being made.

[1]  R. C. Johnson,et al.  Identification of two functional regions in Fis: the N‐terminus is required to promote Hin‐mediated DNA inversion but not lambda excision. , 1991, The EMBO journal.

[2]  R. Gourse,et al.  Involvement of Fis protein in replication of the Escherichia coli chromosome , 1992, Journal of bacteriology.

[3]  R. Gourse,et al.  DNA determinants of rRNA synthesis in E. coli: Growth rate dependent regulation, feedback inhibition, upstream activation, antitermination , 1986, Cell.

[4]  T. Bickle,et al.  Purification and DNA-binding properties of FIS and Cin, two proteins required for the bacteriophage P1 site-specific recombination system, cin. , 1987, Journal of molecular biology.

[5]  R. C. Johnson,et al.  Configuration of DNA strands and mechanism of strand exchange in the Hin invertasome as revealed by analysis of recombinant knots. , 1991, Genes & development.

[6]  M. Simon,et al.  Hin-mediated site-specific recombination requires two 26 by recombination sites and a 60 by recombinational enhancer , 1985, Cell.

[7]  The molecular structure of wild-type and a mutant Fis protein: relationship between mutational changes and recombinational enhancer function or DNA binding. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[8]  W. Saenger,et al.  Three-dimensional structure of the E. coli DMA-binding protein FIS , 1991, Nature.

[9]  R. Kahmann,et al.  G inversion in bacteriophage Mu DNA is stimulated by a site within the invertase gene and a host factor , 1985, Cell.

[10]  R. C. Johnson,et al.  The Hin invertasome: protein-mediated joining of distant recombination sites at the enhancer. , 1990, Science.

[11]  W. Arber,et al.  Mutational analysis of a prokaryotic recombinational enhancer element with two functions. , 1989, The EMBO journal.

[12]  W. Reznikoff Catabolite gene activator protein activation of lac transcription , 1992, Journal of bacteriology.

[13]  L. Bosch,et al.  FIS-induced bending of a region upstream of the promoter activates transcription of the E coli thrU(tufB) operon. , 1991, Biochimie.

[14]  M. Simon,et al.  DNA-binding properties of the Hin recombinase. , 1989, The Journal of biological chemistry.

[15]  A. Klippel,et al.  Isolation and characterization of unusual gin mutants. , 1988, The EMBO journal.

[16]  J. Vandekerckhove,et al.  Escherichia coli host factor for site-specific DNA inversion: cloning and characterization of the fis gene. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[17]  L. Bosch,et al.  FIS-dependent trans-activation of tRNA and rRNA operons of Escherichia coli. , 1990, Biochimica et biophysica acta.

[18]  R. C. Johnson Mechanism of site-specific DNA inversion in bacteria. , 1991, Current opinion in genetics & development.

[19]  L. Bosch,et al.  FIS-dependent trans activation of stable RNA operons of Escherichia coli under various growth conditions , 1992, Journal of bacteriology.

[20]  C. Ball,et al.  Efficient excision of phage lambda from the Escherichia coli chromosome requires the Fis protein , 1991, Journal of bacteriology.

[21]  W. Reznikoff,et al.  Fis plays a role in Tn5 and IS50 transposition , 1992, Journal of bacteriology.

[22]  T. Bickle,et al.  Enhancer‐independent mutants of the Cin recombinase have a relaxed topological specificity. , 1988, The EMBO journal.

[23]  T. Steitz,et al.  Cooperativity mutants of the γδ resolvase identify an essential interdimer interaction , 1990, Cell.

[24]  R. Gourse,et al.  Both fis-dependent and factor-independent upstream activation of the rrnB P1 promoter are face of the helix dependent. , 1992, Nucleic acids research.

[25]  C. Koch,et al.  The Escherichia coli protein, Fis: specific binding to the ends of phage Mu DNA and modulation of phage growth , 1989, Molecular microbiology.

[26]  W. Messer,et al.  The FIS protein binds and bends the origin of chromosomal DNA replication, oriC, of Escherichia coli. , 1991, Nucleic acids research.

[27]  J. F. Thompson,et al.  Empirical estimation of protein-induced DNA bending angles: applications to lambda site-specific recombination complexes. , 1988, Nucleic acids research.

[28]  Johnf . Thompson,et al.  Cellular factors couple recombination with growth phase: Characterization of a new component in the λ site-specific recombination pathway , 1987, Cell.

[29]  A. Landy Dynamic, structural, and regulatory aspects of lambda site-specific recombination. , 1989, Annual review of biochemistry.

[30]  Thomas E. Numrych,et al.  A genetic analysis of Xis and FIS interactions with their binding sites in bacteriophage lambda , 1991, Journal of bacteriology.

[31]  L. Bosch,et al.  Potential binding sites of the trans-activator FIS are present upstream of all rRNA operons and of many but not all tRNA operons. , 1990, Biochimica et biophysica acta.

[32]  R. Plasterk,et al.  The invertible P‐DNA segment in the chromosome of Escherichia coli. , 1985, The EMBO journal.

[33]  R Kahmann,et al.  The E.coli fis promoter is subject to stringent control and autoregulation. , 1992, The EMBO journal.

[34]  R. Gourse,et al.  E.coli Fis protein activates ribosomal RNA transcription in vitro and in vivo. , 1990, The EMBO journal.

[35]  N. Cozzarelli,et al.  Gin-mediated DNA inversion: product structure and the mechanism of strand exchange. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[36]  L. Bosch,et al.  The role of FIS in trans activation of stable RNA operons of E. coli. , 1990, The EMBO journal.

[37]  C. Ball,et al.  Dramatic changes in Fis levels upon nutrient upshift in Escherichia coli , 1992, Journal of bacteriology.

[38]  C. Ball,et al.  Multiple effects of Fis on integration and the control of lysogeny in phage lambda , 1991, Journal of bacteriology.

[39]  Thomas E. Numrych,et al.  Characterization of the bacteriophage lambda excisionase (Xis) protein: the C‐terminus is required for Xis‐integrase cooperativity but not for DNA binding. , 1992, The EMBO journal.

[40]  C. Ball,et al.  Isolation of the gene encoding the Hin recombinational enhancer binding protein. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[41]  M. Simon,et al.  Fis binding to the recombinational enhancer of the Hin DNA inversion system. , 1987, Genes & development.

[42]  N. Cozzarelli,et al.  Processive recombination by the phage Mu Gin system: Implications for the mechanisms of DNA strand exchange, DNA site alignment, and enhancer action , 1990, Cell.

[43]  R. Kahmann,et al.  The N-terminal part of the E.coli DNA binding protein FIS is essential for stimulating site-specific DNA inversion but is not required for specific DNA binding. , 1991, Nucleic acids research.