Bacterial niche-specific genome expansion is coupled with highly frequent gene disruptions in deep-sea sediments.

The complexity and dynamics of microbial metagenomes may be evaluated by genome size, gene duplication and the disruption rate between lineages. In this study, we pyrosequenced the metagenomes of microbes obtained from the brine and sediment of a deep-sea brine pool in the Red Sea to explore the pos...

Full description

Bibliographic Details
Main Authors: Yong Wang, Jiang Ke Yang, On On Lee, Tie Gang Li, Abdulaziz Al-Suwailem, Antoine Danchin, Pei-Yuan Qian
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3244439?pdf=render
_version_ 1818562257755308032
author Yong Wang
Jiang Ke Yang
On On Lee
Tie Gang Li
Abdulaziz Al-Suwailem
Antoine Danchin
Pei-Yuan Qian
author_facet Yong Wang
Jiang Ke Yang
On On Lee
Tie Gang Li
Abdulaziz Al-Suwailem
Antoine Danchin
Pei-Yuan Qian
author_sort Yong Wang
collection DOAJ
description The complexity and dynamics of microbial metagenomes may be evaluated by genome size, gene duplication and the disruption rate between lineages. In this study, we pyrosequenced the metagenomes of microbes obtained from the brine and sediment of a deep-sea brine pool in the Red Sea to explore the possible genomic adaptations of the microbes in response to environmental changes. The microbes from the brine and sediments (both surface and deep layers) of the Atlantis II Deep brine pool had similar communities whereas the effective genome size varied from 7.4 Mb in the brine to more than 9 Mb in the sediment. This genome expansion in the sediment samples was due to gene duplication as evidenced by enrichment of the homologs. The duplicated genes were highly disrupted, on average by 47.6% and 70% for the surface and deep layers of the Atlantis II Deep sediment samples, respectively. The disruptive effects appeared to be mainly due to point mutations and frameshifts. In contrast, the homologs from the Atlantis II Deep brine sample were highly conserved and they maintained relatively small copy numbers. Likely, the adaptation of the microbes in the sediments was coupled with pseudogenizations and possibly functional diversifications of the paralogs in the expanded genomes. The maintenance of the pseudogenes in the large genomes is discussed.
first_indexed 2024-12-14T01:01:20Z
format Article
id doaj.art-050a55827d4c444b8b3ba3ac1c78272f
institution Directory Open Access Journal
issn 1932-6203
language English
last_indexed 2024-12-14T01:01:20Z
publishDate 2011-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj.art-050a55827d4c444b8b3ba3ac1c78272f2022-12-21T23:23:13ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-01612e2914910.1371/journal.pone.0029149Bacterial niche-specific genome expansion is coupled with highly frequent gene disruptions in deep-sea sediments.Yong WangJiang Ke YangOn On LeeTie Gang LiAbdulaziz Al-SuwailemAntoine DanchinPei-Yuan QianThe complexity and dynamics of microbial metagenomes may be evaluated by genome size, gene duplication and the disruption rate between lineages. In this study, we pyrosequenced the metagenomes of microbes obtained from the brine and sediment of a deep-sea brine pool in the Red Sea to explore the possible genomic adaptations of the microbes in response to environmental changes. The microbes from the brine and sediments (both surface and deep layers) of the Atlantis II Deep brine pool had similar communities whereas the effective genome size varied from 7.4 Mb in the brine to more than 9 Mb in the sediment. This genome expansion in the sediment samples was due to gene duplication as evidenced by enrichment of the homologs. The duplicated genes were highly disrupted, on average by 47.6% and 70% for the surface and deep layers of the Atlantis II Deep sediment samples, respectively. The disruptive effects appeared to be mainly due to point mutations and frameshifts. In contrast, the homologs from the Atlantis II Deep brine sample were highly conserved and they maintained relatively small copy numbers. Likely, the adaptation of the microbes in the sediments was coupled with pseudogenizations and possibly functional diversifications of the paralogs in the expanded genomes. The maintenance of the pseudogenes in the large genomes is discussed.http://europepmc.org/articles/PMC3244439?pdf=render
spellingShingle Yong Wang
Jiang Ke Yang
On On Lee
Tie Gang Li
Abdulaziz Al-Suwailem
Antoine Danchin
Pei-Yuan Qian
Bacterial niche-specific genome expansion is coupled with highly frequent gene disruptions in deep-sea sediments.
PLoS ONE
title Bacterial niche-specific genome expansion is coupled with highly frequent gene disruptions in deep-sea sediments.
title_full Bacterial niche-specific genome expansion is coupled with highly frequent gene disruptions in deep-sea sediments.
title_fullStr Bacterial niche-specific genome expansion is coupled with highly frequent gene disruptions in deep-sea sediments.
title_full_unstemmed Bacterial niche-specific genome expansion is coupled with highly frequent gene disruptions in deep-sea sediments.
title_short Bacterial niche-specific genome expansion is coupled with highly frequent gene disruptions in deep-sea sediments.
title_sort bacterial niche specific genome expansion is coupled with highly frequent gene disruptions in deep sea sediments
url http://europepmc.org/articles/PMC3244439?pdf=render
work_keys_str_mv AT yongwang bacterialnichespecificgenomeexpansioniscoupledwithhighlyfrequentgenedisruptionsindeepseasediments
AT jiangkeyang bacterialnichespecificgenomeexpansioniscoupledwithhighlyfrequentgenedisruptionsindeepseasediments
AT ononlee bacterialnichespecificgenomeexpansioniscoupledwithhighlyfrequentgenedisruptionsindeepseasediments
AT tiegangli bacterialnichespecificgenomeexpansioniscoupledwithhighlyfrequentgenedisruptionsindeepseasediments
AT abdulazizalsuwailem bacterialnichespecificgenomeexpansioniscoupledwithhighlyfrequentgenedisruptionsindeepseasediments
AT antoinedanchin bacterialnichespecificgenomeexpansioniscoupledwithhighlyfrequentgenedisruptionsindeepseasediments
AT peiyuanqian bacterialnichespecificgenomeexpansioniscoupledwithhighlyfrequentgenedisruptionsindeepseasediments