R. Thane Papke

Dr. R. Thane Papke


Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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18 July 2003 in Environmental Microbiology
Verified
Journal Article
Closed access
RPR. Thane Papke
R. Thane Papke
NRNiels B. Ramsing
Niels B. Ramsing
MBMary M. Bateson
Mary M. Bateson
DWDavid M. Ward
David M. Ward
WDWard Dm
Ward Dm

1 December 2003 in Annual Review of Genetics
Verified
Journal Article
Closed access
Yann F. BoucherYann F. Boucher
Yann F. Boucher
CDChristophe J. Douady
Christophe J. Douady
RPR. Thane Papke
R. Thane Papke
DWDavid Walsh
David Walsh
MBMary Ellen R. Boudreau
Mary Ellen R. Boudreau
WDW. Ford Doolittle
W. Ford Doolittle
▪ Abstract Lateral gene transfer (LGT) is now known to be a major force in the evolution of prokaryotic genomes. To date, most analyses have focused on either (a) verifying phylogenies of individual genes thought to have been transferred, or (b) estimating the fraction of individual genomes likely to have been introduced by transfer. Neither approach does justice to the ability of LGT to effect massive and complex transformations in basic biology. In some cases, such transformation will be manifested as the patchy distribution of a seemingly fundamental property (such as aerobiosis or nitrogen fixation) among the members of a group classically defined by the sharing of other properties (metabolic, morphological, or molecular, such as small subunit ribosomal RNA sequence). In other cases, the lineage of recipients so transformed may be seen to comprise a new group of high taxonomic rank (“class” or even “phylum”). Here we review evidence for an important role of LGT in the evolution of photosynthesis, aerobic respiration, nitrogen fixation, sulfate reduction, methylotrophy, isoprenoid biosynthesis, quorum sensing, flotation (gas vesicles), thermophily, and halophily. Sometimes transfer of complex gene clusters may have been involved, whereas other times separate exchanges of many genes must be invoked.

9 August 2006 in Genome Research
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Journal Article
Closed access
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OZOlga Zhaxybayeva
Olga Zhaxybayeva
JGJohann Peter Gogarten
Johann Peter Gogarten
RCRobert L. Charlebois
Robert L. Charlebois
WDW. Ford Doolittle
W. Ford Doolittle
RPR. Thane Papke
R. Thane Papke
Using 1128 protein-coding gene families from 11 completely sequenced cyanobacterial genomes, we attempt to quantify horizontal gene transfer events within cyanobacteria, as well as between cyanobacteria and other phyla. A novel method of detecting and enumerating potential horizontal gene transfer events within a group of organisms based on analyses of “embedded quartets” allows us to identify phylogenetic signal consistent with a plurality of gene families, as well as to delineate cases of conflict to the plurality signal, which include horizontally transferred genes. To infer horizontal gene transfer events between cyanobacteria and other phyla, we added homologs from 168 available genomes. We screened phylogenetic trees reconstructed for each of these extended gene families for highly supported monophyly of cyanobacteria (or lack of it). Cyanobacterial genomes reveal a complex evolutionary history, which cannot be represented by a single strictly bifurcating tree for all genes or even most genes, although a single completely resolved phylogeny was recovered from the quartets’ plurality signals. We find more conflicts within cyanobacteria than between cyanobacteria and other phyla. We also find that genes from all functional categories are subject to transfer. However, in interphylum as compared to intraphylum transfers, the proportion of metabolic (operational) gene transfers increases, while the proportion of informational gene transfers decreases.

5 December 2005 in Proceedings of the National Academy of Sciences
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Journal Article
Closed access
EME. F. Mongodin
E. F. Mongodin
KNK. E. Nelson
K. E. Nelson
SDS. Daugherty
S. Daugherty
RDR. T. DeBoy
R. T. DeBoy
JWJ. Wister
J. Wister
FRFrancisco Rodriguez-Valera
Francisco Rodriguez-Valera
Saturated thalassic brines are among the most physically demanding habitats on Earth: few microbes survive in them. Salinibacter ruber is among these organisms and has been found repeatedly in significant numbers in climax saltern crystallizer communities. The phenotype of this bacterium is remarkably similar to that of the hyperhalophilic Archaea (Haloarchaea). The genome sequence suggests that this resemblance has arisen through convergence at the physiological level (different genes producing similar overall phenotype) and the molecular level (independent mutations yielding similar sequences or structures). Several genes and gene clusters also derive by lateral transfer from (or may have been laterally transferred to) haloarchaea. S. ruber encodes four rhodopsins. One resembles bacterial proteorhodopsins and three are of the haloarchaeal type, previously uncharacterized in a bacterial genome. The impact of these modular adaptive elements on the cell biology and ecology of S. ruber is substantial, affecting salt adaptation, bioenergetics, and photobiology.

31 October 2011 in Scientific Reports
Verified
Journal Article
Open access
RGRohit Ghai
Rohit Ghai
LPLejla Pasic
Lejla Pasic
AFAna Beatriz Fernandez
Ana Beatriz Fernandez
AMAna-Belen Martin-Cuadrado
Ana-Belen Martin-Cuadrado
CMCarolina Megumi Mizuno
Carolina Megumi Mizuno
FRFrancisco Rodriguez-Valera
Francisco Rodriguez-Valera
We describe the microbiota of two hypersaline saltern ponds, one of intermediate salinity (19%) and a NaCl saturated crystallizer pond (37%) using pyrosequencing. The analyses of these metagenomes (nearly 784 Mb) reaffirmed the vast dominance of Haloquadratum walsbyi but also revealed novel, abundant and previously unsuspected microbial groups. We describe for the first time, a group of low GC Actinobacteria, related to freshwater Actinobacteria, abundant in low and intermediate salinities. Metagenomic assembly revealed three new abundant microbes: a low-GC euryarchaeon with the lowest GC content described for any euryarchaeon, a high-GC euryarchaeon and a gammaproteobacterium related to Alkalilimnicola and Nitrococcus. Multiple displacement amplification and sequencing of the genome from a single archaeal cell of the new low GC euryarchaeon suggest a photoheterotrophic and polysaccharide-degrading lifestyle and its relatedness to the recently described lineage of Nanohaloarchaea. These discoveries reveal the combined power of an unbiased metagenomic and single cell genomic approach.

25 January 2011 in Nature Communications
Verified
Journal Article
Open access
JBJustin Bahl
Justin Bahl
MVMaggie C.Y. Lau Vetter
Maggie C.Y. Lau Vetter
GSGavin Smith
Gavin Smith
DVDhanasekaran Vijaykrishna
Dhanasekaran Vijaykrishna
SCStephen Cary
Stephen Cary
SPStephen B. Pointing
Stephen B. Pointing
Factors governing large-scale spatio-temporal distribution of microorganisms remain unresolved, yet are pivotal to understanding ecosystem value and function. Molecular genetic analyses have focused on the influence of niche and neutral processes in determining spatial patterns without considering the temporal scale. Here, we use temporal phylogenetic analysis calibrated using microfossil data for a globally sampled desert cyanobacterium, Chroococcidiopsis, to investigate spatio-temporal patterns in microbial biogeography and evolution. Multilocus phylogenetic associations were dependent on contemporary climate with no evidence for distance-related patterns. Massively parallel pyrosequencing of environmental samples confirmed that Chroococcidiopsis variants were specific to either hot or cold deserts. Temporally scaled phylogenetic analyses showed no evidence of recent inter-regional gene flow, indicating populations have not shared common ancestry since before the formation of modern continents. These results indicate that global distribution of desert cyanobacteria has not resulted from widespread contemporary dispersal but is an ancient evolutionary legacy. This highlights the importance of considering temporal scales in microbial biogeography.