2003
DOI: 10.1017/s0953756203008049
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Mycelial incompatibility operative in pairings between single basidiospore isolates of Helicobasidium mompa

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Cited by 18 publications
(9 citation statements)
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“…The pairs from NS non-significant, S significant * (days after inoculation) ** (Weight of fresh mushroom in 3-harvests/weight of dry substrate) 9 100 World J Microbiol Biotechnol (2011) 27:1-9 5 P. eous and P. florida are not included in the further analysis due to the absence of hyphal fusion (barrage formation) between the isolates. It may be the consequence of either the similar mating type of all the isolates or inability of the isolates to fuse with each other under laboratory conditions (Ikeda et al 2002 Four isolates showed compatibility with H23 and one isolate was compatible with H6 (data not shown). All the other isolates were not compatible with the either of the tester isolate (H6 and H23).…”
Section: Identification Of Mating Types Of Single Basidiosporesmentioning
confidence: 96%
“…The pairs from NS non-significant, S significant * (days after inoculation) ** (Weight of fresh mushroom in 3-harvests/weight of dry substrate) 9 100 World J Microbiol Biotechnol (2011) 27:1-9 5 P. eous and P. florida are not included in the further analysis due to the absence of hyphal fusion (barrage formation) between the isolates. It may be the consequence of either the similar mating type of all the isolates or inability of the isolates to fuse with each other under laboratory conditions (Ikeda et al 2002 Four isolates showed compatibility with H23 and one isolate was compatible with H6 (data not shown). All the other isolates were not compatible with the either of the tester isolate (H6 and H23).…”
Section: Identification Of Mating Types Of Single Basidiosporesmentioning
confidence: 96%
“…We used universally primed (UP)-PCR to detect DNA polymorphisms (Bulat et al 2000;Ikeda et al 2003;Ikeda et al 2005) with four primers (AS4, 5 0 -TGTGGGCGCTCGACAG; CA8G, 5 0 -CACACACACACACACAG; AS15inv, 5 0 -CATTGCTGGCGAAA TCGG; GTG, 5 0 -GTGGTGGTGGTGGTG). DNA amplification was performed in a 50 mL reaction mixture containing 1.25 U GoTaq DNA polymerase (Promega, Madison, WI, USA), 1Â PCR buffer, 2.5 mM MgCl 2 , 0.2 mM of each dNTP, 50 ng of template DNA, and 0.35 mM of the UP-PCR primer.…”
Section: Molecular Markers To Elucidate Paternitymentioning
confidence: 99%
“…In most Basidiomycetes, the proliferation of the dikaryon is accompanied by the formation of clamp cells that ensure the proper distribution of the genetically diverse nuclei. However, although widespread, clamps are not essential for the maintenance of a heterokaryotic mycelium; clampless dikaryons have been described in various cases (Swiezynski and Day, 1960a;Kemp, 1980;Salo et al, 1989), especially for various Uredinomycetes (for recent examples, see Frieders and McLaughlin, 2001;Ikeda et al, 2003). Similarly, it was generally believed that in U. maydis clamps are not required for dikaryotic growth.…”
Section: Clamp Formation In Ustilago Maydismentioning
confidence: 99%