Please use this identifier to cite or link to this item: https://doi.org/10.1038/ncomms14444
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dc.titleInnovation and constraint leading to complex multicellularity in the Ascomycota
dc.contributor.authorNguyen, T.A
dc.contributor.authorCissé, O.H
dc.contributor.authorYun Wong, J
dc.contributor.authorZheng, P
dc.contributor.authorHewitt, D
dc.contributor.authorNowrousian, M
dc.contributor.authorStajich, J.E
dc.contributor.authorJedd, G
dc.date.accessioned2020-09-04T03:42:25Z
dc.date.available2020-09-04T03:42:25Z
dc.date.issued2017
dc.identifier.citationNguyen, T.A, Cissé, O.H, Yun Wong, J, Zheng, P, Hewitt, D, Nowrousian, M, Stajich, J.E, Jedd, G (2017). Innovation and constraint leading to complex multicellularity in the Ascomycota. Nature Communications 8 : 14444. ScholarBank@NUS Repository. https://doi.org/10.1038/ncomms14444
dc.identifier.issn2041-1723
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/174433
dc.description.abstractThe advent of complex multicellularity (CM) was a pivotal event in the evolution of animals, plants and fungi. In the fungal Ascomycota, CM is based on hyphal filaments and arose in the Pezizomycotina. The genus Neolecta defines an enigma: phylogenetically placed in a related group containing mostly yeasts, Neolecta nevertheless possesses Pezizomycotina-like CM. Here we sequence the Neolecta irregularis genome and identify CM-associated functions by searching for genes conserved in Neolecta and the Pezizomycotina, which are absent or divergent in budding or fission yeasts. This group of 1,050 genes is enriched for functions related to diverse endomembrane systems and their organization. Remarkably, most show evidence for divergence in both yeasts. Using functional genomics, we identify new genes involved in fungal complexification. Together, these data show that rudimentary multicellularity is deeply rooted in the Ascomycota. Extensive parallel gene divergence during simplification and constraint leading to CM suggest a deterministic process where shared modes of cellular organization select for similarly configured organelle- and transport-related machineries. © The Author(s) 2017.
dc.publisherNature Publishing Group
dc.sourceUnpaywall 20200831
dc.subjectdivergence
dc.subjectevolution
dc.subjectgene expression
dc.subjectgenome
dc.subjectgenomics
dc.subjectinnovation
dc.subjectphylogenetics
dc.subjectyeast
dc.subjectbudding
dc.subjectcell organelle
dc.subjectfission yeast
dc.subjectfunctional genomics
dc.subjectgenetic variability
dc.subjectgenome
dc.subjectmachine
dc.subjectPezizomycotina
dc.subjectAscomycetes
dc.subjectbiodiversity
dc.subjectbiology
dc.subjectcytology
dc.subjectfungal genome
dc.subjectgenetics
dc.subjectmolecular evolution
dc.subjectphylogeny
dc.subjectphysiology
dc.subjectsequence alignment
dc.subjecttransport at the cellular level
dc.subjectwhole genome sequencing
dc.subjectAnimalia
dc.subjectAscomycota
dc.subjectFungi
dc.subjectNeolecta
dc.subjectNeolecta irregularis
dc.subjectPezizomycotina
dc.subjectSchizosaccharomycetaceae
dc.subjectfungal DNA
dc.subjectfungal protein
dc.subjectAscomycota
dc.subjectBiodiversity
dc.subjectBiological Transport
dc.subjectComputational Biology
dc.subjectDNA, Fungal
dc.subjectEvolution, Molecular
dc.subjectFungal Proteins
dc.subjectGenome, Fungal
dc.subjectPhylogeny
dc.subjectSequence Alignment
dc.subjectWhole Genome Sequencing
dc.typeArticle
dc.contributor.departmentBIOLOGY (NU)
dc.description.doi10.1038/ncomms14444
dc.description.sourcetitleNature Communications
dc.description.volume8
dc.description.page14444
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