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Light-dependent expression of four cryptic archaeal circadian gene homologs

Circadian rhythms are important biological signals that have been found in almost all major groups of life from bacteria to man, yet it remains unclear if any members of the second major prokaryotic domain of life, the Archaea, also possess a biological clock. As an initial investigation of this que...

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Autores principales: Maniscalco, Michael, Nannen, Jennifer, Sodi, Valerie, Silver, Gillian, Lowrey, Phillip L., Bidle, Kelly A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941300/
https://www.ncbi.nlm.nih.gov/pubmed/24624125
http://dx.doi.org/10.3389/fmicb.2014.00079
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author Maniscalco, Michael
Nannen, Jennifer
Sodi, Valerie
Silver, Gillian
Lowrey, Phillip L.
Bidle, Kelly A.
author_facet Maniscalco, Michael
Nannen, Jennifer
Sodi, Valerie
Silver, Gillian
Lowrey, Phillip L.
Bidle, Kelly A.
author_sort Maniscalco, Michael
collection PubMed
description Circadian rhythms are important biological signals that have been found in almost all major groups of life from bacteria to man, yet it remains unclear if any members of the second major prokaryotic domain of life, the Archaea, also possess a biological clock. As an initial investigation of this question, we examined the regulation of four cyanobacterial-like circadian gene homologs present in the genome of the haloarchaeon Haloferax volcanii. These genes, designated cirA, cirB, cirC, and cirD, display similarity to the KaiC-family of cyanobacterial clock proteins, which act to regulate rhythmic gene expression and to control the timing of cell division. Quantitative RT-PCR analysis was used to examine the expression of each of the four cir genes in response to 12 h light/12 h dark cycles (LD 12:12) in H. volcanii during balanced growth. Our data reveal that there is an approximately two to sixteen-fold increase in cir gene expression when cells are shifted from light to constant darkness, and this pattern of gene expression oscillates with the light conditions in a rhythmic manner. Targeted single- and double-gene knockouts in the H. volcanii cir genes result in disruption of light-dependent, rhythmic gene expression, although it does not lead to any significant effect on growth under these conditions. Restoration of light-dependent, rhythmic gene expression was demonstrated by introducing, in trans, a wild-type copy of individual cir genes into knockout strains. These results are noteworthy as this is the first attempt to characterize the transcriptional expression and regulation of the ubiquitous kaiC homologs found among archaeal genomes.
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spelling pubmed-39413002014-03-12 Light-dependent expression of four cryptic archaeal circadian gene homologs Maniscalco, Michael Nannen, Jennifer Sodi, Valerie Silver, Gillian Lowrey, Phillip L. Bidle, Kelly A. Front Microbiol Microbiology Circadian rhythms are important biological signals that have been found in almost all major groups of life from bacteria to man, yet it remains unclear if any members of the second major prokaryotic domain of life, the Archaea, also possess a biological clock. As an initial investigation of this question, we examined the regulation of four cyanobacterial-like circadian gene homologs present in the genome of the haloarchaeon Haloferax volcanii. These genes, designated cirA, cirB, cirC, and cirD, display similarity to the KaiC-family of cyanobacterial clock proteins, which act to regulate rhythmic gene expression and to control the timing of cell division. Quantitative RT-PCR analysis was used to examine the expression of each of the four cir genes in response to 12 h light/12 h dark cycles (LD 12:12) in H. volcanii during balanced growth. Our data reveal that there is an approximately two to sixteen-fold increase in cir gene expression when cells are shifted from light to constant darkness, and this pattern of gene expression oscillates with the light conditions in a rhythmic manner. Targeted single- and double-gene knockouts in the H. volcanii cir genes result in disruption of light-dependent, rhythmic gene expression, although it does not lead to any significant effect on growth under these conditions. Restoration of light-dependent, rhythmic gene expression was demonstrated by introducing, in trans, a wild-type copy of individual cir genes into knockout strains. These results are noteworthy as this is the first attempt to characterize the transcriptional expression and regulation of the ubiquitous kaiC homologs found among archaeal genomes. Frontiers Media S.A. 2014-03-04 /pmc/articles/PMC3941300/ /pubmed/24624125 http://dx.doi.org/10.3389/fmicb.2014.00079 Text en Copyright © 2014 Maniscalco, Nannen, Sodi, Silver, Lowrey and Bidle. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Maniscalco, Michael
Nannen, Jennifer
Sodi, Valerie
Silver, Gillian
Lowrey, Phillip L.
Bidle, Kelly A.
Light-dependent expression of four cryptic archaeal circadian gene homologs
title Light-dependent expression of four cryptic archaeal circadian gene homologs
title_full Light-dependent expression of four cryptic archaeal circadian gene homologs
title_fullStr Light-dependent expression of four cryptic archaeal circadian gene homologs
title_full_unstemmed Light-dependent expression of four cryptic archaeal circadian gene homologs
title_short Light-dependent expression of four cryptic archaeal circadian gene homologs
title_sort light-dependent expression of four cryptic archaeal circadian gene homologs
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3941300/
https://www.ncbi.nlm.nih.gov/pubmed/24624125
http://dx.doi.org/10.3389/fmicb.2014.00079
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