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  • 1
    Online Resource
    Online Resource
    Proceedings of the National Academy of Sciences ; 2009
    In:  Proceedings of the National Academy of Sciences Vol. 106, No. 10 ( 2009-03-10), p. 3859-3864
    In: Proceedings of the National Academy of Sciences, Proceedings of the National Academy of Sciences, Vol. 106, No. 10 ( 2009-03-10), p. 3859-3864
    Abstract: Nearly all of eukaryotic diversity has been classified into 6 suprakingdom-level groups (supergroups) based on molecular and morphological/cell-biological evidence; these are Opisthokonta, Amoebozoa, Archaeplastida, Rhizaria, Chromalveolata, and Excavata. However, molecular phylogeny has not provided clear evidence that either Chromalveolata or Excavata is monophyletic, nor has it resolved the relationships among the supergroups. To establish the affinities of Excavata, which contains parasites of global importance and organisms regarded previously as primitive eukaryotes, we conducted a phylogenomic analysis of a dataset of 143 proteins and 48 taxa, including 19 excavates. Previous phylogenomic studies have not included all major subgroups of Excavata, and thus have not definitively addressed their interrelationships. The enigmatic flagellate Andalucia is sister to typical jakobids. Jakobids (including Andalucia ), Euglenozoa and Heterolobosea form a major clade that we name Discoba. Analyses of the complete dataset group Discoba with the mitochondrion-lacking excavates or “metamonads” (diplomonads, parabasalids, and Preaxostyla), but not with the final excavate group, Malawimonas . This separation likely results from a long-branch attraction artifact. Gradual removal of rapidly-evolving taxa from the dataset leads to moderate bootstrap support (69%) for the monophyly of all Excavata, and 90% support once all metamonads are removed. Most importantly, Excavata robustly emerges between unikonts (Amoebozoa + Opisthokonta) and “megagrouping” of Archaeplastida, Rhizaria, and chromalveolates. Our analyses indicate that Excavata forms a monophyletic suprakingdom-level group that is one of the 3 primary divisions within eukaryotes, along with unikonts and a megagroup of Archaeplastida, Rhizaria, and the chromalveolate lineages.
    Type of Medium: Online Resource
    ISSN: 0027-8424 , 1091-6490
    RVK:
    RVK:
    Language: English
    Publisher: Proceedings of the National Academy of Sciences
    Publication Date: 2009
    detail.hit.zdb_id: 209104-5
    detail.hit.zdb_id: 1461794-8
    SSG: 11
    SSG: 12
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  • 2
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 2005
    In:  Systematic Biology Vol. 54, No. 6 ( 2005-12-01), p. 900-915
    In: Systematic Biology, Oxford University Press (OUP), Vol. 54, No. 6 ( 2005-12-01), p. 900-915
    Type of Medium: Online Resource
    ISSN: 1076-836X , 1063-5157
    RVK:
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2005
    detail.hit.zdb_id: 1482572-7
    detail.hit.zdb_id: 1123455-6
    SSG: 12
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  • 3
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2005
    In:  BMC Bioinformatics Vol. 6, No. 1 ( 2005-12)
    In: BMC Bioinformatics, Springer Science and Business Media LLC, Vol. 6, No. 1 ( 2005-12)
    Abstract: Assignment of function to new molecular sequence data is an essential step in genomics projects. The usual process involves similarity searches of a given sequence against one or more databases, an arduous process for large datasets. Results We present AutoFACT, a fully automated and customizable annotation tool that assigns biologically informative functions to a sequence. Key features of this tool are that it (1) analyzes nucleotide and protein sequence data; (2) determines the most informative functional description by combining multiple BLAST reports from several user-selected databases; (3) assigns putative metabolic pathways, functional classes, enzyme classes, GeneOntology terms and locus names; and (4) generates output in HTML, text and GFF formats for the user's convenience. We have compared AutoFACT to four well-established annotation pipelines. The error rate of functional annotation is estimated to be only between 1–2%. Comparison of AutoFACT to the traditional top-BLAST-hit annotation method shows that our procedure increases the number of functionally informative annotations by approximately 50%. Conclusion AutoFACT will serve as a useful annotation tool for smaller sequencing groups lacking dedicated bioinformatics staff. It is implemented in PERL and runs on LINUX/UNIX platforms. AutoFACT is available at http://megasun.bch.umontreal.ca/Software/AutoFACT.htm .
    Type of Medium: Online Resource
    ISSN: 1471-2105
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2005
    detail.hit.zdb_id: 2041484-5
    SSG: 12
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  • 4
    Online Resource
    Online Resource
    Oxford University Press (OUP) ; 2007
    In:  Systematic Biology Vol. 56, No. 2 ( 2007-04-01), p. 194-205
    In: Systematic Biology, Oxford University Press (OUP), Vol. 56, No. 2 ( 2007-04-01), p. 194-205
    Type of Medium: Online Resource
    ISSN: 1076-836X , 1063-5157
    RVK:
    Language: English
    Publisher: Oxford University Press (OUP)
    Publication Date: 2007
    detail.hit.zdb_id: 1482572-7
    detail.hit.zdb_id: 1123455-6
    SSG: 12
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  • 5
    Online Resource
    Online Resource
    The Royal Society ; 2013
    In:  Proceedings of the Royal Society B: Biological Sciences Vol. 280, No. 1769 ( 2013-10-22), p. 20131755-
    In: Proceedings of the Royal Society B: Biological Sciences, The Royal Society, Vol. 280, No. 1769 ( 2013-10-22), p. 20131755-
    Abstract: Most eukaryotic lineages belong to one of a few major groups. However, several protistan lineages have not yet been robustly placed in any of these groups. Both the breviates and apusomonads are two such lineages that appear to be related to the Amoebozoa and Opisthokonta (i.e. the ‘unikonts’ or Amorphea); however, their precise phylogenetic positions remain unclear. Here, we describe a novel microaerophilic breviate, Pygsuia biforma gen. nov. sp. nov . , isolated from a hypoxic estuarine sediment. Ultrastructurally, this species resembles the breviate genera Breviata and Subulatomonas but has two cell morphologies, adherent and swimming. Phylogenetic analyses of the small sub-unit rRNA gene show that Pygsuia is the sister to the other breviates. We constructed a 159-protein supermatrix, including orthologues identified in RNA-seq data from Pygsuia . Phylogenomic analyses of this dataset show that breviates, apusomonads and Opisthokonta form a strongly supported major eukaryotic grouping we name the Obazoa. Although some phylogenetic methods disagree, the balance of evidence suggests that the breviate lineage forms the deepest branch within Obazoa. We also found transcripts encoding a nearly complete integrin adhesome from Pygsuia , indicating that this protein complex involved in metazoan multicellularity may have evolved earlier in eukaryote evolution than previously thought.
    Type of Medium: Online Resource
    ISSN: 0962-8452 , 1471-2954
    Language: English
    Publisher: The Royal Society
    Publication Date: 2013
    detail.hit.zdb_id: 1460975-7
    SSG: 12
    SSG: 25
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  • 6
    Online Resource
    Online Resource
    Springer Science and Business Media LLC ; 2010
    In:  Molecular Genetics and Genomics Vol. 283, No. 1 ( 2010-1)
    In: Molecular Genetics and Genomics, Springer Science and Business Media LLC, Vol. 283, No. 1 ( 2010-1)
    Type of Medium: Online Resource
    ISSN: 1617-4615 , 1617-4623
    Language: English
    Publisher: Springer Science and Business Media LLC
    Publication Date: 2010
    detail.hit.zdb_id: 1462070-4
    SSG: 12
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  • 7
    Online Resource
    Online Resource
    Cold Spring Harbor Laboratory ; 2004
    In:  RNA Vol. 10, No. 4 ( 2004-04), p. 615-621
    In: RNA, Cold Spring Harbor Laboratory, Vol. 10, No. 4 ( 2004-04), p. 615-621
    Abstract: The jakobid flagellates are bacteriovorus protists with mitochondrial genomes that are the most ancestral identified to date, in that they most resemble the genomes of the α-proteobacterial ancestors of the mitochondrion. Because of the bacterial character of jakobid mitochondrial genomes, it was expected that mechanisms for gene expression and RNA structures would be bacterial in nature. However, sequencing of the mitochondrial genome of the jakobid Seculamonas ecuadoriensis revealed several apparent mismatches in the acceptor stems of two predicted tRNAs. To investigate this observation, we determined the cDNA sequences of these tRNAs by RT-PCR. Our results show that the last three positions of the 3′ extremity, plus the discriminator position of seryl and glutamyl tRNAs, are altered posttranscriptionally, restoring orthodox base-pairing and replacing the discriminator with an adenosine residue, in an editing process that resembles that of the metazoan Lithobius forficatus . However, the most 5′ of the edited nucleotides is occasionally left unedited, indicating that the editing mechanism proceeds initially by exonucleolytic degradation, followed by repair of the degraded region. This 3′ tRNA editing mechanism is likely distinct from that of L. forficatus , despite the apparent similarities between the two systems.
    Type of Medium: Online Resource
    ISSN: 1355-8382 , 1469-9001
    Language: English
    Publisher: Cold Spring Harbor Laboratory
    Publication Date: 2004
    detail.hit.zdb_id: 1475737-0
    SSG: 12
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  • 8
    Online Resource
    Online Resource
    Cold Spring Harbor Laboratory ; 2004
    In:  RNA Vol. 10, No. 8 ( 2004-08), p. 1191-1199
    In: RNA, Cold Spring Harbor Laboratory, Vol. 10, No. 8 ( 2004-08), p. 1191-1199
    Abstract: 5′ tRNA editing has been demonstrated to occur in the mitochondria of the distantly related rhizopod amoeba Acanthamoeba castellanii and the chytridiomycete fungus Spizellomyces punctatus . In these organisms, canonical tRNA structures are restored by removing mismatched nucleotides at the first three 5′ positions and replacing them with nucleotides capable of forming Watson–Crick base pairs with their 3′ counterparts. This form of editing seems likely to occur in members of Amoebozoa other than A. castellanii , as well as in members of Heterolobosea. Evidence for 5′ tRNA editing has not been found to date, however, in any other fungus including the deeply branching chytridiomycete Allomyces macrogynus . We predicted that a similar form of tRNA editing would occur in members of the chytridiomycete order Monoblepharidales based on the analysis of complete mitochondrial tRNA complements. This prediction was confirmed by analysis of tRNA sequences using a tRNA circularization/ RT-PCR-based approach. The presence of partially and completely unedited tRNAs in members of the Monoblepharidales suggests the involvement of a 5′-to-3′ exonuclease rather than an endonuclease in removing the three 5′ nucleotides from a tRNA substrate. Surprisingly, analysis of the mtDNA of the chytridiomycete Rhizophydium brooksianum , which branches as a sister group to S. punctatus in molecular phylogenies, did not suggest the presence of editing. This prediction was also confirmed experimentally. The absence of tRNA editing in R. brooksianum raises the possibility that 5′ tRNA editing may have evolved twice independently within Chytridiomycota, once in the lineage leading to S. punctatus and once in the lineage leading to the Monoblepharidales.
    Type of Medium: Online Resource
    ISSN: 1355-8382 , 1469-9001
    Language: English
    Publisher: Cold Spring Harbor Laboratory
    Publication Date: 2004
    detail.hit.zdb_id: 1475737-0
    SSG: 12
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  • 9
    Online Resource
    Online Resource
    Cold Spring Harbor Laboratory ; 2005
    In:  RNA Vol. 11, No. 5 ( 2005-05), p. 785-795
    In: RNA, Cold Spring Harbor Laboratory, Vol. 11, No. 5 ( 2005-05), p. 785-795
    Abstract: We systematically examined transcription and RNA-processing in mitochondria of the petite-negative fission yeast Schizosaccharomyces pombe . Two presumptive transcription initiation sites at opposite positions on the circular-mapping mtDNA were confirmed by in vitro capping of primary transcripts with guanylyl-transferase. The major promoter (P ma ) is located adjacent to the 5′-end of the rnl gene, and a second, minor promoter (P mi ) upstream from cox3 . The primary 5′-termini of the mature rnl and cox3 transcripts remain unmodified. A third predicted accessory transcription initiation site is within the group IIA1 intron of the cob gene ( cob I1). The consensus promoter motif of S. pombe closely resembles the nonanucleotide promoter motifs of various yeast mtDNAs. We further characterized all mRNAs and the two ribosomal RNAs by Northern hybridization, and precisely mapped their 5′- and 3′-ends. The mRNAs have leader sequences with a length of 38 up to 220 nt and, in most instances, are created by removal of tRNAs from large precursor RNAs. Like cox2 and rnl , cox1 and cox3 are not separated by tRNA genes; instead, transcription initiation from the promoters upstream from rnl and cox3 compensates for the lack of tRNA-mediated 5′-processing. The 3′-termini of mRNAs and of SSU rRNA are processed at distinct, C-rich motifs that are located at a variable distance (1–15 nt) downstream from mRNA and SSU-rRNA coding regions. The accuracy of RNA-processing at these sites is sequence-dependent. Similar 3′-RNA-processing motifs are present in species of the genus Schizosaccharomyces , but not in budding yeasts that have functionally analogous A+T-rich dodecamer processing signals.
    Type of Medium: Online Resource
    ISSN: 1355-8382 , 1469-9001
    Language: English
    Publisher: Cold Spring Harbor Laboratory
    Publication Date: 2005
    detail.hit.zdb_id: 1475737-0
    SSG: 12
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  • 10
    Online Resource
    Online Resource
    Elsevier BV ; 2012
    In:  Protist Vol. 163, No. 5 ( 2012-09), p. 746-754
    In: Protist, Elsevier BV, Vol. 163, No. 5 ( 2012-09), p. 746-754
    Type of Medium: Online Resource
    ISSN: 1434-4610
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2012
    detail.hit.zdb_id: 1419415-6
    detail.hit.zdb_id: 2036014-9
    detail.hit.zdb_id: 3033701-X
    SSG: 12
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