New candidates for regulated gene integrity revealed through precise mapping of integrative genetic elements

Author:

Mageeney Catherine M1,Lau Britney Y1,Wagner Julian M1,Hudson Corey M1,Schoeniger Joseph S1,Krishnakumar Raga1,Williams Kelly P1ORCID

Affiliation:

1. Sandia National Laboratories, Systems Biology Department, Livermore, CA 94551-0969, USA

Abstract

Abstract Integrative genetic elements (IGEs) are mobile multigene DNA units that integrate into and excise from host bacterial genomes. Each IGE usually targets a specific site within a conserved host gene, integrating in a manner that preserves target gene function. However, a small number of bacterial genes are known to be inactivated upon IGE integration and reactivated upon excision, regulating phenotypes of virulence, mutation rate, and terminal differentiation in multicellular bacteria. The list of regulated gene integrity (RGI) cases has been slow-growing because IGEs have been challenging to precisely and comprehensively locate in genomes. We present software (TIGER) that maps IGEs with unprecedented precision and without attB site bias. TIGER uses a comparative genomic, ping-pong BLAST approach, based on the principle that the IGE integration module (i.e. its int-attP region) is cohesive. The resultant IGEs from 2168 genomes, along with integrase phylogenetic analysis and gene inactivation tests, revealed 19 new cases of genes whose integrity is regulated by IGEs (including dut, eccCa1, gntT, hrpB, merA, ompN, prkA, tqsA, traG, yifB, yfaT and ynfE), as well as recovering previously known cases (in sigK, spsM, comK, mlrA and hlb genes). It also recovered known clades of site-promiscuous integrases and identified possible new ones.

Funder

Sandia National Laboratories

National Technology and Engineering Solutions of Sandia LLC

U.S. Department of Energy's National Nuclear Security Administration

DARPA Safe Genes

Publisher

Oxford University Press (OUP)

Subject

Genetics

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