Comparative molecular evolution of chitinases in ascomycota with emphasis on mycoparasitism lifestyle.
Comparative molecular evolution of chitinases in ascomycota with emphasis on mycoparasitism lifestyle.
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子囊菌几丁质酶的比较分子进化,重点是真菌寄生生活方式
DOI:
10.1099/mgen.0.000646
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发表时间:
2021-09
影响因子:
3.9
通讯作者:
Zhuang WY
中科院分区:
文献类型:
--
作者:
Wang C;Zeng ZQ;Zhuang WY
Chitinases are involved in multiple aspects of fungal life cycle, such as cell wall remodelling, chitin degradation and mycoparasitism lifestyle. To improve our knowledge of the chitinase molecular evolution of Ascomycota, the gene family of 72 representatives of this phylum was identified and subjected to phylogenetic, evolution trajectory and selective pressure analyses. Phylogenetic analysis showed that the chitinase gene family size and enzyme types varied significantly, along with species evolution, especially for groups B and C. In addition, two new subgroups, C3 and C4, are recognized in group C chitinases. Random birth and death testing indicated that gene expansion and contraction occurred in most of the taxa, particularly for species in the order Hypocreales (class Sordariomycetes). From an enzyme function point of view, we speculate that group A chitinases are mainly involved in species growth and development, while the expansion of genes in group B chitinases is related to fungal mycoparasitic and entomopathogenic abilities, and, to a certain extent, the expansion of genes in group C chitinases seems to be correlated with the host range broadening of some plant-pathogenic fungi in Sordariomycetes. Further selection pressure testing revealed that chitinases and the related amino acid sites were under positive selection in the evolutionary history, especially at the nodes sharing common ancestors and the terminal branches of Hypocreales. These results give a reasonable explanation for the size and function differences of chitinase genes among ascomycetes, and provide a scientific basis for understanding the evolutionary trajectories of chitinases, particularly that towards a mycoparasitic lifestyle.
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影响因子:
12.3
作者:
Kubicek CP;Herrera-Estrella A;Seidl-Seiboth V;Martinez DA;Druzhinina IS;Thon M;Zeilinger S;Casas-Flores S;Horwitz BA;Mukherjee PK;Mukherjee M;Kredics L;Alcaraz LD;Aerts A;Antal Z;Atanasova L;Cervantes-Badillo MG;Challacombe J;Chertkov O;McCluskey K;Coulpier F;Deshpande N;von Döhren H;Ebbole DJ;Esquivel-Naranjo EU;Fekete E;Flipphi M;Glaser F;Gómez-Rodríguez EY;Gruber S;Han C;Henrissat B;Hermosa R;Hernández-Oñate M;Karaffa L;Kosti I;Le Crom S;Lindquist E;Lucas S;Lübeck M;Lübeck PS;Margeot A;Metz B;Misra M;Nevalainen H;Omann M;Packer N;Perrone G;Uresti-Rivera EE;Salamov A;Schmoll M;Seiboth B;Shapiro H;Sukno S;Tamayo-Ramos JA;Tisch D;Wiest A;Wilkinson HH;Zhang M;Coutinho PM;Kenerley CM;Monte E;Baker SE;Grigoriev IV
通讯作者:
Grigoriev IV
影响因子:
9.5
作者:
Katoh K;Rozewicki J;Yamada KD
通讯作者:
Yamada KD
影响因子:
3.2
作者:
Bolar, JP;Norelli, JL;Aldwinckle, HS
通讯作者:
Aldwinckle, HS
影响因子:
10.7
作者:
Janiak, Mareike C.;Chaney, Morgan E.;Tosi, Anthony J.
通讯作者:
Tosi, Anthony J.
DOI:
10.1073/pnas.91.23.10903
发表时间:
1994-11-08
影响因子:
11.1
作者:
CARSOLIO, C;GUTIERREZ, A;HERRERAESTRELLA, A
通讯作者:
HERRERAESTRELLA, A