Global versus Local Regulatory Roles for Lrp-Related Proteins: Haemophilus influenzae as a Case Study

Author:

Friedberg Devorah1,Midkiff Michael1,Calvo Joseph M.1

Affiliation:

1. Section of Biochemistry, Molecular and Cell Biology, Cornell University, Ithaca, New York 14853

Abstract

ABSTRACT Lrp (leucine-responsive regulatory protein) plays a global regulatory role in Escherichia coli , affecting expression of dozens of operons. Numerous lrp -related genes have been identified in different bacteria and archaea, including asnC , an E. coli gene that was the first reported member of this family. Pairwise comparisons of amino acid sequences of the corresponding proteins shows an average sequence identity of only 29% for the vast majority of comparisons. By contrast, Lrp-related proteins from enteric bacteria show more than 97% amino acid identity. Is the global regulatory role associated with E. coli Lrp limited to enteric bacteria? To probe this question we investigated LrfB, an Lrp-related protein from Haemophilus influenzae that shares 75% sequence identity with E. coli Lrp (highest sequence identity among 42 sequences compared). A strain of H. influenzae having an lrfB null allele grew at the wild-type growth rate but with a filamentous morphology. A comparison of two-dimensional (2D) electrophoretic patterns of proteins from parent and mutant strains showed only two differences (comparable studies with lrp + and lrp E. coli strains by others showed 20 differences). The abundance of LrfB in H. influenzae , estimated by Western blotting experiments, was about 130 dimers per cell (compared to 3,000 dimers per E. coli cell). LrfB expressed in E. coli replaced Lrp as a repressor of the lrp gene but acted only to a limited extent as an activator of the ilvIH operon. Thus, although LrfB resembles Lrp sufficiently to perform some of its functions, its low abundance is consonant with a more local role in regulating but a few genes, a view consistent with the results of the 2D electrophoretic analysis. We speculate that an Lrp having a global regulatory role evolved to help enteric bacteria adapt to their ecological niches and that it is unlikely that Lrp-related proteins in other organisms have a broad regulatory function.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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