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Article Addendum

Maintaining heterokaryosis in pseudo-homothallic fungi

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Article: e994382 | Received 24 Oct 2014, Accepted 06 Nov 2014, Published online: 31 Aug 2015

References

  • Billiard S, Lopez-Villavicencio M, Devier B, Hood ME, Fairhead C, Giraud T. Having sex, yes, but with whom? Inferences from fungi on the evolution of anisogamy and mating types. Biol Rev Camb Philos Soc 2011; 86:421–42; PMID:21489122; http://dx.doi.org/10.1111/j.1469-185X.2010.00153.x
  • Attanayake RN, Tennekoon V, Johnson DA, Porter LD, Del Rio-Mendoza L, Jiang D, Chen W. Inferring outcrossing in the homothallic fungus Sclerotinia sclerotiorum using linkage disequilibrium decay. Heredity (Edinb) 2014; 113:353–63; PMID:24781807; http://dx.doi.org/10.1038/hdy.2014.37
  • Haber JE. Mating-type genes and MAT switching in Saccharomyces cerevisiae. Genetics 2012; 191:33–64; PMID:22555442; http://dx.doi.org/10.1534/genetics.111.134577
  • Klar AJ. Regulation of fission yeast mating-type interconversion by chromosome imprinting. Dev Suppl 1990:3–8; PMID:2090428; http://dev.biologists.org/content/108/Supplement/3.full.pdf+html
  • Debuchy R, Berteaux-Lecellier V, Silar P. Mating Systems and Sexual Morphogenesis in Ascomycetes. In: Borkovich K, Ebbole D, eds. Cellular and Molecular Biology of Filamentous Fungi. Washington, DC: ASM Press, 2010:501–35.
  • Raju NB, Perkins DD. Diverse programs of ascus development in pseudohomothallic species of Neurospora, Gelasinospora, and Podospora. Dev Genet 1994; 15:104–18; PMID:8187347; http://dx.doi.org/10.1002/dvg.1020150111
  • Langton FA, Elliott TJ. Genetics of secondarily homothallic basidiomycetes. Heredity 1980; 45:99–106; http://dx.doi.org/10.1038/hdy.1980.53
  • Dodge BO. Spermatia and nuclear migration in Pleurage anserina. Mycologia 1936; 28:284–91; http://dx.doi.org/10.2307/3754278
  • Rizet G, Engelmann C. Contribution à l'étude génétique d'un Ascomycète tétrasporé : Podospora anserina (Ces.) Rehm. Rev Cytol Biol Veg 1949; 11:201–304.
  • Dodge B. Nuclear phenomena associated with heterothallism and homothallism in the ascomycete Neurospora. J Agr Res 1927; 35:289–305.
  • Colson B. The Cytology and Morphology of Neurospora tetrasperma Dodge. Annals of Botany 1934; os-48:211–24.
  • Duncan EG, Galbraith M. Post-meiotic events in the Homobasidiomycetidae. Trans Brit Mycol Soc 1972; 58:387–92; http://dx.doi.org/10.1016/S0007-1536(72)80088-3
  • Kamzolkina OV, Volkova VN, Kozlova MV, Pancheva EV, Dyakov YT, Callac P. Karyological evidence for meiosis in the three different types of life cycles existing in Agaricus bisporus. Mycologia 2006; 98:763–70; PMID:17256579; http://dx.doi.org/10.3852/mycologia.98.5.763
  • Challen MP, Elliott TJ. Segregation of genetic markers in the two-spored secondarily homothallic basidiomycete Coprinus bilanatus. Theor Appl Genet 1989; 78:601–7; PMID:24225691; http://dx.doi.org/10.1007/BF00290848
  • Summerbell RC, Castle AJ, Horgen PA, Anderson JB. Inheritance of restriction fragment length polymorphisms in Agaricus brunnescens. Genetics 1989; 123:293–300; PMID:2573557.
  • Poggeler S. Phylogenetic relationships between mating-type sequences from homothallic and heterothallic ascomycetes. Curr Genet 1999; 36:222–31; PMID:10541860; http://dx.doi.org/10.1007/s002940050494
  • Picard M, Debuchy R, Coppin E. Cloning the mating types of the heterothallic fungus Podospora anserina: developmental features of haploid transformants carrying both mating types. Genetics 1991; 128:539–47; PMID:1831427.
  • Ellison CE, Stajich JE, Jacobson DJ, Natvig DO, Lapidus A, Foster B, Aerts A, Riley R, Lindquist EA, Grigoriev IV, et al. Massive changes in genome architecture accompany the transition to self-fertility in the filamentous fungus Neurospora tetrasperma. Genetics 2011; 189:55–69; PMID:21750257; http://dx.doi.org/10.1534/genetics.111.130690
  • Grognet P, Bidard F, Kuchly C, Tong LC, Coppin E, Benkhali JA, Couloux A, Wincker P, Debuchy R, Silar P. Maintaining Two Mating Types: Structure of the Mating Type Locus and Its Role in Heterokaryosis in Podospora anserina. Genetics 2014; 197:421–32; PMID:24558260; http://dx.doi.org/10.1534/genetics.113.159988
  • Xu J, Kerrigan RW, Horgen PA, Anderson JB. Localization of the Mating Type Gene in Agaricus bisporus. Appl Environ Microbiol 1993; 59:3044–9; PMID:16349046.
  • Morin E, Kohler A, Baker AR, Foulongne-Oriol M, Lombard V, Nagy LG, Ohm RA, Patyshakuliyeva A, Brun A, Aerts AL, et al. Genome sequence of the button mushroom Agaricus bisporus reveals mechanisms governing adaptation to a humic-rich ecological niche. Proc Natl Acad Sci U S A 2012; PMID:23045686.
  • Charlesworth D, Charlesworth B, Marais G. Steps in the evolution of heteromorphic sex chromosomes. Heredity (Edinb) 2005; 95:118–28; PMID:15931241; http://dx.doi.org/10.1038/sj.hdy.6800697
  • Branch Howe Jr H. Vegetative Traits Associated with Mating Type in Neurospora tetrasperma. Mycologia 1964; 56:519–25; http://dx.doi.org/10.2307/3756357
  • Samils N, Gioti A, Karlsson M, Sun Y, Kasuga T, Bastiaans E, Wang Z, Li N, Townsend JP, Johannesson H. Sex-linked transcriptional divergence in the hermaphrodite fungus Neurospora tetrasperma. Proc Biol Sci 2013; 280:20130862; PMID:23782882; http://dx.doi.org/10.1098/rspb.2013.0862
  • Contamine V, Zickler D, Picard M. The Podospora rmp1 gene implicated in nucleus-mitochondria cross-talk encodes an essential protein whose subcellular location is developmentally regulated. Genetics 2004; 166:135–50; PMID:15020413; http://dx.doi.org/10.1534/genetics.166.1.135
  • Roper M, Simonin A, Hickey PC, Leeder A, Glass NL. Nuclear dynamics in a fungal chimera. Proc Natl Acad Sci U S A 2013; 110:12875–80; PMID:23861490; http://dx.doi.org/10.1073/pnas.1220842110
  • Corcoran P, Jacobson DJ, Bidartondo MI, Hickey PC, Kerekes JF, Taylor JW, Johannesson H. Quantifying functional heterothallism in the pseudohomothallic ascomycete Neurospora tetrasperma. Fungal Biol 2012; 116:962–75; PMID:22954339; http://dx.doi.org/10.1016/j.funbio.2012.06.006
  • Colson B. The Cytology of the Mushroom Psalliota campestris Quel. Annals of Botany 1935; os-49:1–18.
  • Kligman AM. Some Cultural and Genetic Problems in the Cultivation of the Mushroom, Agaricus campestris Fr. American Journal of Botany 1943; 30:745–63; http://dx.doi.org/10.2307/2437548
  • Callac P, Billette C, Imbernon M, Kerrigan RW. Morphological, Genetic, and Interfertility Analyses Reveal a Novel, Tetrasporic Variety of Agaricus bisporus from the Sonoran Desert of California. Mycologia 1993; 85:835–51; http://dx.doi.org/10.2307/3760617
  • Dodge BO. Inheritance of the Albinistic Non-Conidial Characters in Interspecific Hybrids in Neurospora. Mycologia 1931; 23:1–50.
  • Howe HB, Jr. Markers and centromere distances in Neurospora tetrasperma. Genetics 1963; 48:121–31; PMID:13955153.
  • Howe HB, Jr. Sources of Error in Genetic Analysis in Neurospora Tetrasperma. Genetics 1964; 50:181–9; PMID:14191349.
  • Dowding ES. The sexuality of the normal, giant and dwarf spores of Pleurage anserina. (Ces) Kuntze. Ann Bot 1931; 45:1–14.
  • Beckett A. The ascus with an apical pore: Development, Composition, and Function. In: DR R, ed. Ascomycetes Systematics - The Luttrellian concept. New York, Heildelberg, Berlin: Springer verlag, 1981:7–26.
  • Thompson-Coffe C, Zickler D. Cytoskeleton interactions in the ascus development and sporulation of Sordaria macrospora. J Cell Sci 1993; 104:883–98.
  • Richard F, Glass NL, Pringle A. Cooperation among germinating spores facilitates the growth of the fungus, Neurospora crassa. Biol Lett 2012; 8:419-22; PMID: 22258449; http://dx.doi.org/10.1098/rsbl.2011.1141
  • Hou H, Wu L. Nuclear behaviour of cultivated mushroom. Bot Bull Academia Sinica 1972; 13:82–91.