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Mating-type genes from the homothallic fungus Sordaria macrospora are functionally expressed in a heterothallic ascomycete.
Pöggeler S, Risch S, Kück U, Osiewacz HD. Pöggeler S, et al. Genetics. 1997 Oct;147(2):567-80. Genetics. 1997. PMID: 9335594 Free PMC article.
To determine functionality of the S. macrospora mating-type genes, we show that all ORFs are transcriptionally expressed. Furthermore, we transformed the S. macrospora mating-type genes into mat- and mat+ strains of the closely related heterothallic fungus P. anseri …
To determine functionality of the S. macrospora mating-type genes, we show that all ORFs are transcriptionally expressed. Furthermore …
Cell differentiation during sexual development of the fungus Sordaria macrospora requires ATP citrate lyase activity.
Nowrousian M, Masloff S, Pöggeler S, Kück U. Nowrousian M, et al. Mol Cell Biol. 1999 Jan;19(1):450-60. doi: 10.1128/mcb.19.1.450. Mol Cell Biol. 1999. PMID: 9858569 Free PMC article.
The molecular mass of the S. macrospora ACL1 polypeptide is 73 kDa, as was verified by Western blot analysis with a hemagglutinin (HA) epitope-tagged ACL1 polypeptide. ...We discuss the contribution of ACL activity to the life cycle of S. macrospora....
The molecular mass of the S. macrospora ACL1 polypeptide is 73 kDa, as was verified by Western blot analysis with a hemagglutinin (HA …
Comparative analysis of the mating-type loci from Neurospora crassa and Sordaria macrospora: identification of novel transcribed ORFs.
Pöggeler S, Kück U. Pöggeler S, et al. Mol Gen Genet. 2000 Mar;263(2):292-301. doi: 10.1007/s004380051171. Mol Gen Genet. 2000. PMID: 10778748
In this study, we describe the comparative transcriptional analysis of the chimeric mating-type region of S. macrospora and the corresponding region of the N. crassa mat a idiomorph. ...The same mode of transcription was found in the corresponding mating-type region of …
In this study, we describe the comparative transcriptional analysis of the chimeric mating-type region of S. macrospora and the corre …
Two pheromone precursor genes are transcriptionally expressed in the homothallic ascomycete Sordaria macrospora.
Pöggeler S. Pöggeler S. Curr Genet. 2000 Jun;37(6):403-11. doi: 10.1007/s002940000120. Curr Genet. 2000. PMID: 10905431
Both genes are expressed during the life cycle of S. macrospora. This is the first description of pheromone precursor genes encoded by a homothallic fungus. ...
Both genes are expressed during the life cycle of S. macrospora. This is the first description of pheromone precursor genes encoded b …
Mating-type genes for classical strain improvements of ascomycetes.
Pöggeler S. Pöggeler S. Appl Microbiol Biotechnol. 2001 Sep;56(5-6):589-601. doi: 10.1007/s002530100721. Appl Microbiol Biotechnol. 2001. PMID: 11601605 Review.
Identification of transcriptionally expressed pheromone receptor genes in filamentous ascomycetes.
Pöggeler S, Kück U. Pöggeler S, et al. Gene. 2001 Dec 12;280(1-2):9-17. doi: 10.1016/s0378-1119(01)00786-7. Gene. 2001. PMID: 11738813
The deduced pre2 product displays significant sequence similarity with the S. cerevisiae STE2 gene product, the alpha-factor receptor. Pair-wise comparisons between pheromone receptor genes of N. crassa and S. macrospora revealed an extremely low degree of nucleotid …
The deduced pre2 product displays significant sequence similarity with the S. cerevisiae STE2 gene product, the alpha-factor receptor …
Functional analysis of the C6 zinc finger gene pro1 involved in fungal sexual development.
Masloff S, Jacobsen S, Pöggeler S, Kück U. Masloff S, et al. Fungal Genet Biol. 2002 Jul;36(2):107-16. doi: 10.1016/S1087-1845(02)00010-5. Fungal Genet Biol. 2002. PMID: 12081464
To further characterize the PRO1 polypeptide, the yeast system was used for identifying a transactivation domain in the N-terminal half of PRO1, which probably also functions in S. macrospora. ...When a N. crassa pro1 cDNA clone was used in complementation transformations, …
To further characterize the PRO1 polypeptide, the yeast system was used for identifying a transactivation domain in the N-terminal half of P …
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