ライフサイエンスコーパス: Ascomycota

1 ary multicellularity is deeply rooted in the Ascomycota.

2 eiled a 13-residue sequence conserved across Ascomycota.

3 ely missing in two major phyla, nematoda and ascomycota.

4 e three functionally related networks in the Ascomycota.

5 ships between major groups within the phylum Ascomycota.

6 58%, respectively) fungal species within the Ascomycota.

7 including both yeast-forming and filamentous Ascomycota.

8 with different preferences for Basidio- and Ascomycota.

9 izontal gene transfer events, primarily from Ascomycota.

10 mpared gene repertoires to related groups in Ascomycota.

11 Among the Ascomycota, 65 genera were identified, and the abundant

12 Here we investigate the Teloschistales (Ascomycota), a group of >1,000 lichenized species with v

13 t a phylogenetic comparative analysis of the Ascomycota, a phylum that includes greater than 98% of k

14 Ascomycota account for about two-thirds of named fungal

15 trunk diseases (GTDs) are caused by diverse Ascomycota and Basidiomycota fungal pathogens in at leas

16 Our results showed that GH28 phylogeny of Ascomycota and Basidiomycota sequences was structured by

17 In fungal phyla, Ascomycota and Basidiomycota were significantly more abu

18 subkingdom of Fungi that includes the phyla Ascomycota and Basidiomycota) in this site is scant.

19 ities were dominated by members of the phyla Ascomycota and Basidiomycota, and also by Chytridiomycot

20 rse taxonomic and ecological groups from the Ascomycota and Basidiomycota, and furthermore, if those

21 erophilic fungi including taxa grouping into Ascomycota and Basidiomycota, capable of displacing salt

22 for respective sporocarps of ectomycorrhizal Ascomycota and Basidiomycota, however, with an offset to

23 orphic fungal isolates, representing diverse Ascomycota and Basidiomycota, to resist exposure to five

24 dividing budding yeasts of two major phyla: Ascomycota and Basidiomycota.

25 omycetota; fungal communities were primarily Ascomycota and Basidiomycota.

26 cteriota and Proteobacteria and fungal phyla Ascomycota and Basidiomycota.

27 ria, and Proteobacteria and the fungal phyla Ascomycota and genus Basidiobolus.

28 munity, which in both years was dominated by Ascomycota and Mortierellomycota.

29 profiles in 15 yeast species from the phylum Ascomycota and reconstruct the evolution of their modula

30 ingdom Fungi are contained in two phyla, the Ascomycota and the Basidiomycota (subkingdom Dikarya).

31 iomycota), symbiotrophism and saprotrophism (Ascomycota) and pathotrophism (Chytridiomycota) with ele

32 across multiple lineages of Mucoromycotina, Ascomycota, and Basidiomycota.

33 a minimum node age calibration point for the Ascomycota as a whole, or even the Dikarya crown group,

34 f largest subphylum of Fungi-Pezizomycotina (Ascomycota)-based on sequence alignments for six loci (n

35 Within the fungal community, Ascomycota, Basidiomycota and Chytridiomycota were the m

36 in of the major groups of terrestrial fungi (Ascomycota, Basidiomycota, and Glomales) around 600 mill

37 common ancestor of three major fungal phyla-Ascomycota, Basidiomycota, and Mucoromycota.

38 rom species across the fungal kingdom (e.g., Ascomycota, Basidiomycota, and non-Dikarya taxa), 36,399

39 hly enriched in moldy homes and 14 taxa from Ascomycota, Basidiomycota, and Zygomycota that were more

40 splicing mechanisms seen in the fungal phyla Ascomycota, Basidiomycota, and Zygomycota.

41 con sequence variants dominated by the phyla Ascomycota, Basidiomycota, Mortierellomycota and Chytrid

42 They were dominated by the phyla Ascomycota, Basidiomycota, Mortierellomycota and Mucorom

43 uence variants (ASVs) representing the phyla Ascomycota, Basidiomycota, Mortierellomycota, Chytridiom

44 uence variants (ASVs) dominated by the phyla Ascomycota, Basidiomycota, Mortierellomycota, Mucoromyco

45 ommunities in all lakes; however, members of Ascomycota, Basidiomycota, Zygomycota, and Blastocladiom

46 The ratio of Ascomycota/Basidiomycota significantly decreased along w

47 f named fungal species.(1) Over 98% of known Ascomycota belong to the Pezizomycotina, including many

48 cies within subphylum Pezizomycotina (phylum Ascomycota) but not early diverging ascomycetes, like Sa

49 studies are related to the G2/M phase of the Ascomycota cell cycle; the third is related to morphogen

50 anning several fungal classes, including the Ascomycota classes, Eurotiomycetes, Sordariomycetes, Sac

51 fic hybrid endophytes of the genus Epichloe (Ascomycota, Clavicipitaceae) are prevalent in wild grass

52 In the fungal Ascomycota, CM is based on hyphal filaments and arose in

53 The fungal phylum Ascomycota comprises three subphyla: Saccharomycotina, P

54 cormycota constituted 56% of infections, and Ascomycota constituted 37%.

55 stly belonging to wind dispersed, generalist Ascomycota, dominate soils globally.

56 of lichenization have been infrequent during Ascomycota evolution, but have been followed by multiple

57 in polar environments were the most abundant Ascomycota found and their occurrence in native wood sam

58 es that would target individual layers of an Ascomycota fungal cell wall.

59 l response to heat shock in eight species of Ascomycota fungi and to reconstruct modules of the ances

60 Our results show that Ascomycota fungi are causing extensive soft rot decay at

61 genome-wide nucleosome occupancy maps in 13 Ascomycota fungi to discover large-scale evolutionary re

62 d with them are surprisingly diverged across Ascomycota fungi.

63 s were also laterally transferred to certain Ascomycota, Glomeromycota, Viridiplantae, and Amoebozoa.

64 ifferent from other lichen-forming fungi and Ascomycota groups in general, which may reflect the evol

65 ctarius spp. dominated the endosphere, while Ascomycota, Hypocreales and Giberella spp. dominated the

66 ungest dune, transitioning to a dominance of Ascomycota in both soil horizons.

67 Cyanobacteria in bacteria and the phylum of Ascomycota in fungi.

68 gh melanin necromass of Hyaloscypha bicolor (Ascomycota) in liquid cultures and assessed T. reesei ge

69 that we attribute to Ascomycota incertae sedis (Dikarya).

70 c classification chosen, 15-18 orders of the Ascomycota include lichen-forming taxa, and 8-11 of thes

71 n members of the Pezizomycotina subphylum of Ascomycota, including the human pathogen Aspergillus fum

72 parasitic fungus in the genus Columnomyces (Ascomycota, Laboulbeniales), triggered an investigation

73 As a consequence, major Ascomycota lineages of exclusively non-lichen-forming sp

74 Fungal taxa belonging to Ascomycota, Mortierellomycota, Archaeorhizomycetes, Doth

75 istory of the Parmeliaceae (Lecanoromycetes, Ascomycota), one of the largest families of lichen-formi

76 ually exclusive presence of either the phyla Ascomycota or Basiodiomycota.

77 l development, and appressorium formation in Ascomycota pathogens, B. cinerea, M. oryzae, Sclerotinia

78 longing to the Chaetothyriales order and the Ascomycota phylum, are known for their capability to inh

79 , as Saccharomyces cerevisiae belongs to the ascomycota phylum.

80 Basidiomycota was lowest in winter, whereas Ascomycota predominated in the same season.

81 e Dikarya crown group, along with some other Ascomycota previously documented in the Rhynie Chert.

82 mmunity were found, and the Basidiomycota to Ascomycota ratio was related to mean temperature of the

83 these orders (representing about 60% of the Ascomycota species) contain both lichenized and non-lich

84 stinct mechanisms, conserved across multiple Ascomycota species, by which this molecular adaptation o

85 the Rhizoplaca melanophthalma (Lecanoraceae, Ascomycota) species complex.

86 ury ago but its precise placement within the Ascomycota still remains uncertain.

87 ingly, this site of methylation is unique to Ascomycota, suggesting a recent evolutionary innovation

88 ngal isolates obtained were identified as 29 Ascomycota taxa by sequencing different regions of DNA.

89 We identified 11 Ascomycota taxa that were more highly enriched in moldy

90 es represent distinct lineages of the phylum Ascomycota that independently evolved a "yeast" life cyc

91 One family within the Euascomycetes (Ascomycota), the lichen-forming Physciaceae, is particul

92 ylum Saccharomycotina (Kingdom Fungi, Phylum Ascomycota) to explore signatures of convergent evolutio

93 Most OTUs assignments corresponded to Ascomycota, unidentified fungi and Basidiomycota.

94 Among fungal communities, phylum Ascomycota was prevalent in the rhizosphere and endosphe

95 Phylum Ascomycota was significantly abundant in non-degraded so

96 The results showed that Ascomycota was the dominant fungal phylum in Chinese Cor

97 sociated with AT while Microbacteriaceae and Ascomycota were enriched in DT.

98 Eleven orders of the phylum Ascomycota were identified: Pleosporales (the largest gr

99 Members of the Ascomycota were most dominant, though the exact function

100 s have smaller genomes than most filamentous Ascomycota, with reduced arsenals of carbohydrate-degrad

101 oss each of the fungal phyla (Basidiomycota, Ascomycota, Zygomycota, Chytridomycota and Glomeromycota