Home LiteratureArticle Details
PMID: 3015719 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Genetical and molecular analyses of qa-2 transformants in Neurospora crassa.

Genetics ·Vol. 113 ·No. 3 ·1986-07-00 ·Pages 569-87

Case ME

Abstract

Neurospora crassa qa-2+ transformants from five different donor DNA clones were analyzed by genetical and molecular techniques. None of the 32 transformants have the qa-2+ DNA replacing the qa-2- gene in linkage group VII. In one transformant, the qa-2+ DNA was inserted adjacent to the qa-2- gene. Thirty-one transformants have the qa-2+ inserts at sites not linked, or not closely linked, to the qa-2 locus in LG VII. Plasmid sequences were integrated along with the qa-2+ gene in 28 transformants. In the unlinked duplication-type transformants, catabolic dehydroquinase (the qa-2+ gene product) was induced at 5-100% of the wild-type-induced enzyme activity, with 24 transformants in the 5-80% range. The reduced levels of enzyme activity may be due to "position effects" of sequences adjacent to the integration site either in the N. crassa genomic DNA or in the flanking plasmid (pBR322 or pBR325) sequences. Unexpected gene conversion-like events, in which a qa-2+ gene was changed to qa-2-, were observed in tetrads from intercrosses between unlinked duplication-type transformants and in selfings of such transformants.

MeSH Terms
Cloning, Molecular DNA Restriction Enzymes DNA Transposable Elements Genes, Fungal Genetic Linkage Neurospora/genetics Neurospora crassa/genetics Nucleic Acid Hybridization Plasmids Transformation, Genetic
Chemicals
DNA Transposable Elements DNA Restriction Enzymes
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Case M E
References (10)
10 references, click to expand
  1. Detection of specific sequences among DNA fragments separated by gel electrophoresis.
    J Mol Biol. 1975 Nov 5;98(3):503-17 PMID: 1195397
  2. A general method for isolation of high molecular weight DNA from eukaryotes.
    Nucleic Acids Res. 1976 Sep;3(9):2303-8 PMID: 987581
  3. Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I.
    J Mol Biol. 1977 Jun 15;113(1):237-51 PMID: 881736
  4. Transcription and translation in E. coli of hybrid plasmids containing the catabolic dehydroquinase gene from Neurospora crassa.
    Gene. 1978 Nov;4(3):241-59 PMID: 154430
  5. ALLELIC RECOMBINATION IN NEUROSPORA: TETRAD ANALYSIS OF A THREE-POINT CROSS WITHIN THE PAN-2 LOCUS.
    Genetics. 1964 Mar;49:529-40 PMID: 14135412
  6. Sequence variation in dispersed repetitive sequences in Saccharomyces cerevisiae.
    J Mol Biol. 1981 Feb 5;145(4):619-32 PMID: 7021854
  7. Identification and characterization of recombinant plasmids carrying the complete qa gene cluster from Neurospora crassa including the qa-1+ regulatory gene.
    Proc Natl Acad Sci U S A. 1981 Aug;78(8):5086-90 PMID: 6272290
  8. Point mutations and DNA rearrangements 5' to the inducible qa-2 gene of Neurospora allow activator protein-independent transcription.
    Proc Natl Acad Sci U S A. 1983 Dec;80(23):7298-302 PMID: 6316356
  9. Transformation of Neurospora crassa with the cloned am (glutamate dehydrogenase) gene.
    Mol Cell Biol. 1984 Jan;4(1):117-22 PMID: 6230518
  10. Gene conversion of the mating-type locus in Saccharomyces cerevisiae.
    Genetics. 1979 Jul;92(3):777-82 PMID: 395021
Article Info
Journal
Genetics
Abbr.
Genetics
ISSN
0016-6731
Published
1986-07-00
Pages
569-87
Language
English
Region
United States
NLM ID
0374636
PMCID
PMC1202856
Subset
IM
Grants
NIGMS NIH HHS · GM28777 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: product@genelibs.com