Massive mitochondrial gene transfer in a parasitic flowering plant clade.
Recent studies have suggested that plant genomes have undergone potentially rampant horizontal gene transfer (HGT), especially in the mitochondrial genome. Parasitic plants have provided the strongest evidence of HGT, which appears to be facilitated by the intimate physical association between the p...
Main Authors: | , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2013-01-01
|
Series: | PLoS Genetics |
Online Access: | http://europepmc.org/articles/PMC3573108?pdf=render |
id |
doaj-c69de62fd80d47de8c21ff6c40d82f60 |
---|---|
record_format |
Article |
spelling |
doaj-c69de62fd80d47de8c21ff6c40d82f602020-11-25T00:24:49ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042013-01-0192e100326510.1371/journal.pgen.1003265Massive mitochondrial gene transfer in a parasitic flowering plant clade.Zhenxiang XiYuguo WangRobert K BradleyM SugumaranChristopher J MarxJoshua S RestCharles C DavisRecent studies have suggested that plant genomes have undergone potentially rampant horizontal gene transfer (HGT), especially in the mitochondrial genome. Parasitic plants have provided the strongest evidence of HGT, which appears to be facilitated by the intimate physical association between the parasites and their hosts. A recent phylogenomic study demonstrated that in the holoparasite Rafflesia cantleyi (Rafflesiaceae), whose close relatives possess the world's largest flowers, about 2.1% of nuclear gene transcripts were likely acquired from its obligate host. Here, we used next-generation sequencing to obtain the 38 protein-coding and ribosomal RNA genes common to the mitochondrial genomes of angiosperms from R. cantleyi and five additional species, including two of its closest relatives and two host species. Strikingly, our phylogenetic analyses conservatively indicate that 24%-41% of these gene sequences show evidence of HGT in Rafflesiaceae, depending on the species. Most of these transgenic sequences possess intact reading frames and are actively transcribed, indicating that they are potentially functional. Additionally, some of these transgenes maintain synteny with their donor and recipient lineages, suggesting that native genes have likely been displaced via homologous recombination. Our study is the first to comprehensively assess the magnitude of HGT in plants involving a genome (i.e., mitochondria) and a species interaction (i.e., parasitism) where it has been hypothesized to be potentially rampant. Our results establish for the first time that, although the magnitude of HGT involving nuclear genes is appreciable in these parasitic plants, HGT involving mitochondrial genes is substantially higher. This may represent a more general pattern for other parasitic plant clades and perhaps more broadly for angiosperms.http://europepmc.org/articles/PMC3573108?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Zhenxiang Xi Yuguo Wang Robert K Bradley M Sugumaran Christopher J Marx Joshua S Rest Charles C Davis |
spellingShingle |
Zhenxiang Xi Yuguo Wang Robert K Bradley M Sugumaran Christopher J Marx Joshua S Rest Charles C Davis Massive mitochondrial gene transfer in a parasitic flowering plant clade. PLoS Genetics |
author_facet |
Zhenxiang Xi Yuguo Wang Robert K Bradley M Sugumaran Christopher J Marx Joshua S Rest Charles C Davis |
author_sort |
Zhenxiang Xi |
title |
Massive mitochondrial gene transfer in a parasitic flowering plant clade. |
title_short |
Massive mitochondrial gene transfer in a parasitic flowering plant clade. |
title_full |
Massive mitochondrial gene transfer in a parasitic flowering plant clade. |
title_fullStr |
Massive mitochondrial gene transfer in a parasitic flowering plant clade. |
title_full_unstemmed |
Massive mitochondrial gene transfer in a parasitic flowering plant clade. |
title_sort |
massive mitochondrial gene transfer in a parasitic flowering plant clade. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS Genetics |
issn |
1553-7390 1553-7404 |
publishDate |
2013-01-01 |
description |
Recent studies have suggested that plant genomes have undergone potentially rampant horizontal gene transfer (HGT), especially in the mitochondrial genome. Parasitic plants have provided the strongest evidence of HGT, which appears to be facilitated by the intimate physical association between the parasites and their hosts. A recent phylogenomic study demonstrated that in the holoparasite Rafflesia cantleyi (Rafflesiaceae), whose close relatives possess the world's largest flowers, about 2.1% of nuclear gene transcripts were likely acquired from its obligate host. Here, we used next-generation sequencing to obtain the 38 protein-coding and ribosomal RNA genes common to the mitochondrial genomes of angiosperms from R. cantleyi and five additional species, including two of its closest relatives and two host species. Strikingly, our phylogenetic analyses conservatively indicate that 24%-41% of these gene sequences show evidence of HGT in Rafflesiaceae, depending on the species. Most of these transgenic sequences possess intact reading frames and are actively transcribed, indicating that they are potentially functional. Additionally, some of these transgenes maintain synteny with their donor and recipient lineages, suggesting that native genes have likely been displaced via homologous recombination. Our study is the first to comprehensively assess the magnitude of HGT in plants involving a genome (i.e., mitochondria) and a species interaction (i.e., parasitism) where it has been hypothesized to be potentially rampant. Our results establish for the first time that, although the magnitude of HGT involving nuclear genes is appreciable in these parasitic plants, HGT involving mitochondrial genes is substantially higher. This may represent a more general pattern for other parasitic plant clades and perhaps more broadly for angiosperms. |
url |
http://europepmc.org/articles/PMC3573108?pdf=render |
work_keys_str_mv |
AT zhenxiangxi massivemitochondrialgenetransferinaparasiticfloweringplantclade AT yuguowang massivemitochondrialgenetransferinaparasiticfloweringplantclade AT robertkbradley massivemitochondrialgenetransferinaparasiticfloweringplantclade AT msugumaran massivemitochondrialgenetransferinaparasiticfloweringplantclade AT christopherjmarx massivemitochondrialgenetransferinaparasiticfloweringplantclade AT joshuasrest massivemitochondrialgenetransferinaparasiticfloweringplantclade AT charlescdavis massivemitochondrialgenetransferinaparasiticfloweringplantclade |
_version_ |
1725351372981796864 |