scholarly journals Molecular analysis of the Coprinus cinereus mating type A factor demonstrates an unexpectedly complex structure.

Genetics ◽  
1991 ◽  
Vol 128 (3) ◽  
pp. 529-538 ◽  
Author(s):  
G May ◽  
L Le Chevanton ◽  
P J Pukkila

Abstract We report here the molecular cloning of the A43 mating type factor from Coprinus cinereus, a basidiomycetous fungus. Our molecular analyses revealed an unexpected source of variation in the A factor. Though genetic studies have demonstrated that A has two subunits, alpha and beta, we located three nonoverlapping fragments in the A43 region that have A factor function following DNA-mediated transformation. The three fragments demonstrate no similarity to one another as judged by restriction enzyme maps and by hybridization on Southern blots. We conclude that the A43 factor is composed of at least three subunits. When strains carrying different A factors are examined by hybridization to the cloned subunits, extensive polymorphism is seen. Both intensity of hybridization and restriction fragment lengths vary between strains. Some strains fail to show any hybridization to a probe. In contrast, other strains from widely separated geographic locations apparently share very similar subunits. From comparative restriction enzyme mapping of A43 and a mutated A43 factor, we inferred that a 12-kb deletion in the A factor was responsible for the constitutive, dominant phenotype of the mutated A factor. The results of transformation experiments support an activator model for the activity of the A factor in regulating the A pathway.

1990 ◽  
Vol 18 (3) ◽  
pp. 223-229 ◽  
Author(s):  
E. S. Mutasa ◽  
A. M. Tymon ◽  
B. G�ttgens ◽  
F. M. Mellon ◽  
P. F. R. Little ◽  
...  

1990 ◽  
Vol 18 (3) ◽  
pp. 144-146 ◽  
Author(s):  
Stephen J Higgins ◽  
B David Hames ◽  
Elizabeth McIntosh ◽  
Alan Colman

2021 ◽  
Vol 888 (1) ◽  
pp. 012024
Author(s):  
P W Prihandini ◽  
A Primasari ◽  
M Luthfi ◽  
D Pamungkas ◽  
A P Z N L Sari ◽  
...  

Abstract The restriction enzyme is important for genotyping using the PCR-RFLP technique. Therefore, this study aims to identify the restriction enzyme mapping in the partial sequence of the follicle-stimulating hormone receptor (FSHR) gene in Indonesian local cattle. A total of 29 samples sized 306 bp, were aligned with Genbank sequence acc no. NC_032660, resulting three polymorphic sites, namely g.193G>C, g.227T>C, and g.275A>C. Furthermore, the restriction mapping analysis using the NEBcutter program V2.0 showed that no enzyme recognized the SNP g.275A>C, while the SNP g.193G>C and g.227T>C were identified by the AluI and MscI enzymes, respectively. The AluI enzyme cuts at two positions (193 bp and 243 bp) in the G allele sample producing three fragments namely 50 bp, 63 bp, and 193 bp, meanwhile, in the C allele, the AluI cuts only in position 243 bp, hence, the fragment products are 63 bp and 243 bp. In contrast, the MscI enzyme was only recognized in the T allele, producing fragments sized 77 bp and 229 bp but failed to identify the restriction site along with the PCR products in the C allele. Based on the results, the SNPs (g.193G>C and g.227T>C) and restriction enzymes (AluI and MscI) are applicable for genotyping local Indonesian cattle using the PCR-RFLP technique in future studies.


1992 ◽  
Vol 10 (1) ◽  
pp. 73-82 ◽  
Author(s):  
Michael A. Mallamaci ◽  
David P. Reed ◽  
Stephen A. Winkle

1992 ◽  
Vol 31 (4) ◽  
pp. 343-349 ◽  
Author(s):  
Michael Sheppard ◽  
Sarah M. Drysdale ◽  
Michael J. Studdert

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