Literature DB >> 22169356

Screening for yeast mutants defective in recipient ability for transkingdom conjugation with Escherichia coli revealed importance of vacuolar ATPase activity in the horizontal DNA transfer phenomenon.

Mami Mizuta1, Emi Satoh, Chika Katoh, Katsuyuki Tanaka, Kazuki Moriguchi, Katsunori Suzuki.   

Abstract

Proteobacterium Escherichia coli strains harboring wide-transfer-range conjugative plasmids are able to transfer these plasmids to several yeast species. Whole plasmid DNA is mobilizable in the transkingdom conjugation phenomenon. Owing to the availability of various conjugative plasmids in bacteria, the horizontal DNA transfer has potential to occur between various bacteria and eukaryotes. In order to know host factor genes involved in such conjugation, we systematically tested the conjugability of strains among a yeast library comprising single-gene-knockout mutants in this study. This genome-wide screen identified 26 host chromosomal genes whose absence reduced the efficiency of the transkingdom conjugation. Among the 26 genes, 20 are responsible for vacuolar ATPase activity, while 5 genes (SHP1, CSG2, CCR4, NOT5, and HOF1) seem to play a role in maintaining the cell surface. Lack of either ZUO1 gene or SSZ1 gene, each of which encodes a component of the ribosome-associated cytoplasmic molecular chaperone, also strongly affected transkingdom conjugation.
Copyright © 2011 Elsevier GmbH. All rights reserved.

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Year:  2011        PMID: 22169356     DOI: 10.1016/j.micres.2011.10.001

Source DB:  PubMed          Journal:  Microbiol Res        ISSN: 0944-5013            Impact factor:   5.415


  4 in total

1.  Transkingdom genetic transfer from Escherichia coli to Saccharomyces cerevisiae as a simple gene introduction tool.

Authors:  Kazuki Moriguchi; Noritaka Edahiro; Shinji Yamamoto; Katsuyuki Tanaka; Nori Kurata; Katsunori Suzuki
Journal:  Appl Environ Microbiol       Date:  2013-05-10       Impact factor: 4.792

2.  Trans-kingdom horizontal DNA transfer from bacteria to yeast is highly plastic due to natural polymorphisms in auxiliary nonessential recipient genes.

Authors:  Kazuki Moriguchi; Shinji Yamamoto; Katsuyuki Tanaka; Nori Kurata; Katsunori Suzuki
Journal:  PLoS One       Date:  2013-09-13       Impact factor: 3.240

3.  DNA repair genes RAD52 and SRS2, a cell wall synthesis regulator gene SMI1, and the membrane sterol synthesis scaffold gene ERG28 are important in efficient Agrobacterium-mediated yeast transformation with chromosomal T-DNA.

Authors:  Yuta Ohmine; Yukari Satoh; Kazuya Kiyokawa; Shinji Yamamoto; Kazuki Moriguchi; Katsunori Suzuki
Journal:  BMC Microbiol       Date:  2016-04-02       Impact factor: 3.605

4.  A Fast and Practical Yeast Transformation Method Mediated by Escherichia coli Based on a Trans-Kingdom Conjugal Transfer System: Just Mix Two Cultures and Wait One Hour.

Authors:  Kazuki Moriguchi; Shinji Yamamoto; Yuta Ohmine; Katsunori Suzuki
Journal:  PLoS One       Date:  2016-02-05       Impact factor: 3.240

  4 in total

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