scholarly journals Integrative transformation of Aspergillus oryzae with a plasmid containing the Aspergillus nidulans argB gene.

1987 ◽  
Vol 51 (9) ◽  
pp. 2549-2555 ◽  
Author(s):  
Katsuya GOMI ◽  
Yuzuru IIMURA ◽  
Shodo HARA
2001 ◽  
Vol 39 (3) ◽  
pp. 175-182 ◽  
Author(s):  
Akimitsu Tanaka ◽  
Ken-ichi Kamei ◽  
Stefan Steidl ◽  
Axel A. Brakhage ◽  
Meryl A. Davis ◽  
...  

1991 ◽  
Vol 99 (4) ◽  
pp. 711-719
Author(s):  
K.L. O'Donnell ◽  
A.H. Osmani ◽  
S.A. Osmani ◽  
N.R. Morris

The recessive, temperature-sensitive bimA1 mutation of Aspergillus nidulans blocks nuclei in metaphase at restrictive temperature. To determine whether the bimA product is essential, integrative transformation was used to create a mutation in the bimA gene. The mutation was maintained in a heterokaryon and the phenotype of spores produced by the heterokaryon was analyzed. Molecular disruption of the wild-type bimA gene is recessive in the heterokaryon and causes a metaphase block, demonstrating that bimA is an essential gene for mitosis. bimA was cloned by DNA-mediated complementation of its mutant phenotype at restrictive temperature, and the nucleotide sequence of a full-length cDNA was determined. A single large open reading frame was identified in the cDNA sequence, which predicts a protein containing 806 amino acid residues that is related (30.4% identity) to the Schizosaccharomyces pombe nuc2+ gene product, which also is required for completion of mitosis. The sequence of the bimA gene indicates that it is a member of a family of mostly nuclear proteins that contain a degenerate 34 amino acid repeat, the TPR (tetratricopeptide repeat) gene family.


2016 ◽  
Vol 101 (6) ◽  
pp. 2343-2356 ◽  
Author(s):  
Takumi Tanaka ◽  
Mayumi Nakayama ◽  
Toru Takahashi ◽  
Kei Nanatani ◽  
Youhei Yamagata ◽  
...  

1974 ◽  
Vol 22 (3) ◽  
pp. 183-188 ◽  
Author(s):  
JÜRGEN REISS

In the cells of Aspergillus oryzae, Aspergillus nidulans, Neurospora crassa and Saccharomyces cerevisiae, aryl sulfatase can be demonstrated by incubation in a medium containing 6-bromo-2-naphthylsulfate as substrate and fast garnet GBC as coupling agent. Controls confirm the specificity of the reaction. Other incubation solutions (two Gomori media and a simultaneous coupling procedure with 8-hydroxyquinoline sulfate as substrate) gave negative results or reaction pictures equally to those in substrate-free control. The possible reasons for this are discussed. In the mycelial fungi the strongest enzyme activity is located in the most intensely metabolizing parts: tips of the hyphae and the differentiating parts of the conidiophores. The reaction granules in all four fungi are possibly identical with lysosomes.


Genetics ◽  
1990 ◽  
Vol 124 (3) ◽  
pp. 585-591 ◽  
Author(s):  
G Faugeron ◽  
L Rhounim ◽  
J L Rossignol

Abstract Repeated genes, artificially introduced in Ascobolus immersus by integrative transformation, are frequently inactivated during the sexual phase. Inactivation is observed in about 50% of meioses if duplicated genes are at ectopic chromosomal locations, and in 90% of meioses if genes are tandemly repeated. Inactivation is associated with extensive methylation of the cytosine residues of the duplicated sequences and is induced in the still haploid nuclei of the dikaryotic cell which will undergo karyogamy and subsequent meiosis. Only repeated sequences become methylated. This raises the intriguing question of how the premeiotic inactivation machinery is informed that a nucleus contains multiple copies of a gene. By using in crosses recombinant strains of A. immersus in which either one, two or three genetically independent copies of the exogenous amdS gene from Aspergillus nidulans had been introduced, we could follow the premeiotic inactivation of each one of the ectopic amdS copies. This led us to propose that a prerequisite for inactivation is a premeiotic pairing of repeated sequences and that each copy can undergo successive cycles of pairing. In fact, once methylated, a copy can pair with a still unmethylated copy, so that an uneven number of copies can be subject to inactivation.


1985 ◽  
Vol 101 (3) ◽  
pp. 712-719 ◽  
Author(s):  
G S May ◽  
J Gambino ◽  
J A Weatherbee ◽  
N R Morris

We have cloned two different beta-tubulin sequences from the filamentous fungus Aspergillus nidulans. Each was used in the construction of transforming plasmids that carry the pyr4 gene of Neurospora crassa. We used these plasmids to transform a pyrG-strain of Aspergillus to uridine prototrophy. Both plasmids were shown to integrate site specifically into the homologous chromosomal sequences. We then used transformant strains in genetic crosses to demonstrate that one of the cloned beta-tubulin sequences was the benA beta-tubulin gene, which codes for the beta 1-and beta 2-tubulins. The other cloned beta-tubulin sequence was shown to be the structural gene for beta 3-tubulin by gene disruption and to participate in conidial development. This is the first report of a gene disruption by site specific, integrative recombination in Aspergillus nidulans.


Gene ◽  
2013 ◽  
Vol 525 (1) ◽  
pp. 5-10 ◽  
Author(s):  
Hiromi Nishida ◽  
Takuya Katayama ◽  
Yutaka Suzuki ◽  
Shinji Kondo ◽  
Hiroyuki Horiuchi

2009 ◽  
Vol 46 (1) ◽  
pp. S161-S169 ◽  
Author(s):  
Pedro M. Coutinho ◽  
Mikael R. Andersen ◽  
Katarina Kolenova ◽  
Patricia A. vanKuyk ◽  
Isabelle Benoit ◽  
...  

2011 ◽  
Vol 93 (3) ◽  
pp. 1157-1166 ◽  
Author(s):  
Ines Pisanelli ◽  
Petra Wührer ◽  
Yazmid Reyes-Dominguez ◽  
Oliver Spadiut ◽  
Dietmar Haltrich ◽  
...  

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