189 research outputs found

    Inversion in the published genetic map of linkage group VII

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    In the course of cloning the dim-2 gene of Neurospora crassa we found that the published map of LG VII has an inversion of a segment extending from for to un-10K. Direct physical mapping confirmed that the gene order in this region should be wc-1, for, frq, oli, un-10

    Making the selectable marker bar tighter and more economical

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    Use of the bacterial basta resistance gene (bar) as a selectable marker in Neurospora was reported by Avalos et al (1989 Curr. Genet. 16:369-372)

    Small scale DNA preps for Neurospora crassa

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    Molecular biology experiments often require preparation of small amounts of DNA from many samples. This abbreviated DNA isolation method yields an average of 0.6 micrograms of genomic DNA that is suitable for Southern analysis or PCR. Starting with fresh mycelium, 20 to 40 samples can be processed in approximately two hours. Better yields (about 5 micrograms) may be obtained by suspending approximately 100 microliters of ground lyophilized mycelium in 500 microliters of isolation buffer and following the protocol starting from step 4. Spin refers to centrifugation of samples at 14,000 rpm in a microcentrifuge

    DNA sequence duplications trigger gene inactivation in Neurospora crassa.

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    Improved plasmids for gene targeting at the his-3 locus of Neurospora crassa by electroporation: Correction

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    Two mistakes in our article on gene replacement by gene targeting at the his-3 locus (Margolin, B.S. et al., 1997, FGN 44:34-36) have come to our attention

    Improved plasmids for gene targeting at the his-3 locus of Neurospora crassa by electroporation

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    We report two new plasmids, pBM60 and pBM61, and procedures to efficiently generate single- copy transformants targeted to the his-3 locus in Neurospora crassa

    A simple plating assay for aneuploidy in sexual progeny of Neurospora crassa, and a new allele of mei-1.

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    We developed a simple ascospore plating assay for aneuploidy, based on identifying disomic progeny that inherit two independently selectable mtr alleles. We validated the assay using a known meiotic mutant, mei-2. We used this assay to demonstrate that elevated frequencies of aneuploidy previously reported to be associated with reduced DNA methylation were not, in fact, due to the methylation deficiencies. A new allele of the mei-1 gene was responsible for some of the high aneuploidy

    A method for finding the genetic map position of cloned DNA fragments

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    A method for finding the genetic map position of cloned DNA fragment

    One-Liners

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    One-Liners from P.T. Borgia, J. Irelan and E.U. Selker, and B.C. Turner and A. Fairfiel
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