Matthias Bernt

Dr. Matthias Bernt


Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

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

Representative Publications

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1 November 2013 in Molecular Phylogenetics and Evolution
Verified
Journal Article
Closed access
MBMatthias Bernt
Matthias Bernt
ADAlexander Donath
Alexander Donath
FJFrank Jühling
Frank Jühling
FEFabian Externbrink
Fabian Externbrink
CFCatherine Florentz
Catherine Florentz
Peter F. StadlerPeter F. Stadler
Peter F. Stadler

1 November 2013 in Molecular Phylogenetics and Evolution
Verified
Journal Article
Closed access
MBMatthias Bernt
Matthias Bernt
ABAnke Braband
Anke Braband
BSBernd Schierwater
Bernd Schierwater
Peter F. StadlerPeter F. Stadler
Peter F. Stadler

1 November 2013 in Molecular Phylogenetics and Evolution
Verified
Journal Article
Closed access
MBMatthias Bernt
Matthias Bernt
CBChristoph Bleidorn
Christoph Bleidorn
ABAnke Braband
Anke Braband
JDJohannes Dambach
Johannes Dambach
ADAlexander Donath
Alexander Donath
TSTorsten H. Struck
Torsten H. Struck

1 January 2017 in Molecular Phylogenetics and Evolution
Verified
Journal Article
Closed access
MAMarwa Al Arab
Marwa Al Arab
CSChristian Höner zu Siederdissen
Christian Höner zu Siederdissen
KTKifah Tout
Kifah Tout
ASAbdullah H. Sahyoun
Abdullah H. Sahyoun
Peter F. StadlerPeter F. Stadler
Peter F. Stadler
MBMatthias Bernt
Matthias Bernt

1 July 2014 in Mitochondrion
Verified
Journal Article
Closed access
ASAbdullah H. Sahyoun
Abdullah H. Sahyoun
MBMatthias Bernt
Matthias Bernt
Peter F. StadlerPeter F. Stadler
Peter F. Stadler
KTKifah Tout
Kifah Tout

4 May 2012 in BMC Genomics
Verified
Journal Article
Open access
PDF file
ADAngelo Duò
Angelo Duò
RBRémy Bruggmann
Rémy Bruggmann
SZStefan Zoller
Stefan Zoller
MBMatthias Bernt
Matthias Bernt
CGChristoph R Grünig
Christoph R Grünig
Background: Mitochondrial (mt) markers are successfully applied in evolutionary biology and systematics because mt genomes often evolve faster than the nuclear genomes. In addition, they allow robust phylogenetic analysis based on conserved proteins of the oxidative phosphorylation system. In the present study we sequenced and annotated the complete mt genome of P. subalpina, a member of the Phialocephala fortinii s.l. – Acephala applanata species complex (PAC). PAC belongs to the Helotiales, which is one of the most diverse groups of ascomycetes including more than 2,000 species. The gene order was compared to deduce the mt genome evolution in the Pezizomycotina. Genetic variation in coding and intergenic regions of the mtDNA was studied for PAC to assess the usefulness of mt DNA for species diagnosis. Results: The mt genome of P. subalpina is 43,742 bp long and codes for 14 mt genes associated with the oxidative phosphorylation. In addition, a GIY-YIG endonuclease, the ribosomal protein S3 (Rps3) and a putative N-acetyl-transferase were recognized. A complete set of tRNA genes as well as the large and small rRNA genes but no introns were found. All protein-coding genes were confirmed by EST sequences. The gene order in P. subalpina deviated from the gene order in Sclerotinia sclerotiorum, the only other helotialean species with a fully sequenced and annotated mt genome. Gene order analysis within Pezizomycotina suggests that the evolution of gene orders is mostly driven by transpositions. Furthermore, sequence diversity in coding and non-coding mtDNA regions in seven additional PAC species was pronounced and allowed for unequivocal species diagnosis in PAC. Conclusions: The combination of non-interrupted ORFs and EST sequences resulted in a high quality annotation of the mt genome of P. subalpina, which can be used as a reference for the annotation of other mt genomes in the Helotiales. In addition, our analyses show that mtDNA loci will be the marker of choice for future analysis of PAC communities.