Literature DB >> 8879235

Mild RIP-an alternative method for in vivo mutagenesis of the albino-3 gene in Neurospora crassa.

C Barbato1, M Calissano, A Pickford, N Romano, G Sandmann, G Macino.   

Abstract

We have used a biological phenomenon that occurs in Neurospora crassa, termed Repeat-Induced Point mutation (RIP), to create partially functional mutant alleles of the albino-3 (al-3) gene encoding geranylgeranyl pyrophosphate synthase, an enzyme involved in the biosynthesis of carotenoids and diverse prenylated compounds. A total of 70 RIP-induced al-3 mutants were identified by their pale albino phenotype, resulting from inactivation of carotenoid bio-synthesis. Nucleotide sequence analysis of the al-3 gene in five of the RIP-induced mutants revealed that in each case RIP had introduced no more than six point mutations. The low frequency of RIP mutants (0.42%) and the isolation of only leaky mutants with very few mutations suggest that ascospores containing a heavily mutated al-3 gene do not survive. These results are evidence that the RIP phenomenon, used to inactivate and silence duplicated genes in N. crassa, may be exploited in its mild version as a method of sequence-specific in vivo mutagenesis to obtain functional mutant alleles of Neurospora genes. This mild form of mutagenesis may be particularly advantageous in selecting for leaky mutations in essential Neurospora genes.

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Year:  1996        PMID: 8879235     DOI: 10.1007/bf02172999

Source DB:  PubMed          Journal:  Mol Gen Genet        ISSN: 0026-8925


  36 in total

1.  The Biochemistry and Molecular Biology of Isoprenoid Metabolism.

Authors:  J. Chappell
Journal:  Plant Physiol       Date:  1995-01       Impact factor: 8.340

2.  Quelling: transient inactivation of gene expression in Neurospora crassa by transformation with homologous sequences.

Authors:  N Romano; G Macino
Journal:  Mol Microbiol       Date:  1992-11       Impact factor: 3.501

3.  Repeat-induced G-C to A-T mutations in Neurospora.

Authors:  E B Cambareri; B C Jensen; E Schabtach; E U Selker
Journal:  Science       Date:  1989-06-30       Impact factor: 47.728

4.  Rearrangement of duplicated DNA in specialized cells of Neurospora.

Authors:  E U Selker; E B Cambareri; B C Jensen; K R Haack
Journal:  Cell       Date:  1987-12-04       Impact factor: 41.582

5.  Rapid and efficient cosmid cloning.

Authors:  D Ish-Horowicz; J F Burke
Journal:  Nucleic Acids Res       Date:  1981-07-10       Impact factor: 16.971

6.  Targeted transformation of Ascobolus immersus and de novo methylation of the resulting duplicated DNA sequences.

Authors:  C Goyon; G Faugeron
Journal:  Mol Cell Biol       Date:  1989-07       Impact factor: 4.272

Review 7.  Premeiotic instability of repeated sequences in Neurospora crassa.

Authors:  E U Selker
Journal:  Annu Rev Genet       Date:  1990       Impact factor: 16.830

8.  Efficient cloning of genes of Neurospora crassa.

Authors:  S J Vollmer; C Yanofsky
Journal:  Proc Natl Acad Sci U S A       Date:  1986-07       Impact factor: 11.205

9.  Photoregulation of the Carotenoid Biosynthetic Pathway in Albino and White Collar Mutants of Neurospora crassa.

Authors:  R W Harding; R V Turner
Journal:  Plant Physiol       Date:  1981-09       Impact factor: 8.340

10.  Functional identification of al-3 from Neurospora crassa as the gene for geranylgeranyl pyrophosphate synthase by complementation with crt genes, in vitro characterization of the gene product and mutant analysis.

Authors:  G Sandmann; N Misawa; M Wiedemann; P Vittorioso; A Carattoli; G Morelli; G Macino
Journal:  J Photochem Photobiol B       Date:  1993-05       Impact factor: 6.252

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  1 in total

1.  The BEM46-like protein appears to be essential for hyphal development upon ascospore germination in Neurospora crassa and is targeted to the endoplasmic reticulum.

Authors:  Moritz Mercker; Krisztina Kollath-Leiss; Silke Allgaier; Nancy Weiland; Frank Kempken
Journal:  Curr Genet       Date:  2009-02-24       Impact factor: 3.886

  1 in total

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