Cargando…
Characterization of bacterial operons consisting of two tubulins and a kinesin-like gene by the novel Two-Step Gene Walking method
Tubulins are still considered as typical proteins of Eukaryotes. However, more recently they have been found in the unusual bacteria Prosthecobacter (btubAB). In this study, the genomic organization of the btub-genes and their genomic environment were characterized by using the newly developed Two-S...
Autores principales: | , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2007
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2175320/ https://www.ncbi.nlm.nih.gov/pubmed/17942428 http://dx.doi.org/10.1093/nar/gkm836 |
_version_ | 1782145460096466944 |
---|---|
author | Pilhofer, Martin Bauer, Andreas Peter Schrallhammer, Martina Richter, Lothar Ludwig, Wolfgang Schleifer, Karl-Heinz Petroni, Giulio |
author_facet | Pilhofer, Martin Bauer, Andreas Peter Schrallhammer, Martina Richter, Lothar Ludwig, Wolfgang Schleifer, Karl-Heinz Petroni, Giulio |
author_sort | Pilhofer, Martin |
collection | PubMed |
description | Tubulins are still considered as typical proteins of Eukaryotes. However, more recently they have been found in the unusual bacteria Prosthecobacter (btubAB). In this study, the genomic organization of the btub-genes and their genomic environment were characterized by using the newly developed Two-Step Gene Walking method. In all investigated Prosthecobacters, btubAB are organized in a typical bacterial operon. Strikingly, all btub-operons comprise a third gene with similarities to kinesin light chain sequences. The genomic environments of the characterized btub-operons are always different. This supports the hypothesis that this group of genes represents an independent functional unit, which was acquired by Prosthecobacter via horizontal gene transfer. The newly developed Two-Step Gene Walking method is based on randomly primed polymerase chain reaction (PCR). It presents a simple workflow, which comprises only two major steps—a Walking-PCR with a single specific outward pointing primer (step 1) and the direct sequencing of its product using a nested specific primer (step 2). Two-Step Gene Walking proved to be highly efficient and was successfully used to characterize over 20 kb of sequence not only in pure culture but even in complex non-pure culture samples. |
format | Text |
id | pubmed-2175320 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21753202008-01-07 Characterization of bacterial operons consisting of two tubulins and a kinesin-like gene by the novel Two-Step Gene Walking method Pilhofer, Martin Bauer, Andreas Peter Schrallhammer, Martina Richter, Lothar Ludwig, Wolfgang Schleifer, Karl-Heinz Petroni, Giulio Nucleic Acids Res Methods Online Tubulins are still considered as typical proteins of Eukaryotes. However, more recently they have been found in the unusual bacteria Prosthecobacter (btubAB). In this study, the genomic organization of the btub-genes and their genomic environment were characterized by using the newly developed Two-Step Gene Walking method. In all investigated Prosthecobacters, btubAB are organized in a typical bacterial operon. Strikingly, all btub-operons comprise a third gene with similarities to kinesin light chain sequences. The genomic environments of the characterized btub-operons are always different. This supports the hypothesis that this group of genes represents an independent functional unit, which was acquired by Prosthecobacter via horizontal gene transfer. The newly developed Two-Step Gene Walking method is based on randomly primed polymerase chain reaction (PCR). It presents a simple workflow, which comprises only two major steps—a Walking-PCR with a single specific outward pointing primer (step 1) and the direct sequencing of its product using a nested specific primer (step 2). Two-Step Gene Walking proved to be highly efficient and was successfully used to characterize over 20 kb of sequence not only in pure culture but even in complex non-pure culture samples. Oxford University Press 2007-11 2007-10-16 /pmc/articles/PMC2175320/ /pubmed/17942428 http://dx.doi.org/10.1093/nar/gkm836 Text en © 2007 The Author(s) http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Methods Online Pilhofer, Martin Bauer, Andreas Peter Schrallhammer, Martina Richter, Lothar Ludwig, Wolfgang Schleifer, Karl-Heinz Petroni, Giulio Characterization of bacterial operons consisting of two tubulins and a kinesin-like gene by the novel Two-Step Gene Walking method |
title | Characterization of bacterial operons consisting of two tubulins and a kinesin-like gene by the novel Two-Step Gene Walking method |
title_full | Characterization of bacterial operons consisting of two tubulins and a kinesin-like gene by the novel Two-Step Gene Walking method |
title_fullStr | Characterization of bacterial operons consisting of two tubulins and a kinesin-like gene by the novel Two-Step Gene Walking method |
title_full_unstemmed | Characterization of bacterial operons consisting of two tubulins and a kinesin-like gene by the novel Two-Step Gene Walking method |
title_short | Characterization of bacterial operons consisting of two tubulins and a kinesin-like gene by the novel Two-Step Gene Walking method |
title_sort | characterization of bacterial operons consisting of two tubulins and a kinesin-like gene by the novel two-step gene walking method |
topic | Methods Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2175320/ https://www.ncbi.nlm.nih.gov/pubmed/17942428 http://dx.doi.org/10.1093/nar/gkm836 |
work_keys_str_mv | AT pilhofermartin characterizationofbacterialoperonsconsistingoftwotubulinsandakinesinlikegenebythenoveltwostepgenewalkingmethod AT bauerandreaspeter characterizationofbacterialoperonsconsistingoftwotubulinsandakinesinlikegenebythenoveltwostepgenewalkingmethod AT schrallhammermartina characterizationofbacterialoperonsconsistingoftwotubulinsandakinesinlikegenebythenoveltwostepgenewalkingmethod AT richterlothar characterizationofbacterialoperonsconsistingoftwotubulinsandakinesinlikegenebythenoveltwostepgenewalkingmethod AT ludwigwolfgang characterizationofbacterialoperonsconsistingoftwotubulinsandakinesinlikegenebythenoveltwostepgenewalkingmethod AT schleiferkarlheinz characterizationofbacterialoperonsconsistingoftwotubulinsandakinesinlikegenebythenoveltwostepgenewalkingmethod AT petronigiulio characterizationofbacterialoperonsconsistingoftwotubulinsandakinesinlikegenebythenoveltwostepgenewalkingmethod |