Use of fluorescent protein to analyse recombination at three loci in Neurospora crassa.

doi:10.1016/j.fgb.2012.05.012

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Back to search

Article

Use of fluorescent protein to analyse recombination at three loci in Neurospora crassa.

Fungal genetics and biology : FG & B - 1 Aug 2012

Bowring Frederick J, Yeadon P Jane, Catcheside David E A

Abstract excerpt

We have inserted a histone H1-GFP fusion gene adjacent to three loci on different chromosomes of Neurospora crassa and made mating pairs in which a wild type version of GFP is crossed to one with a mutation in the 5' end of GFP. The loci are his-3, am and his-5, chosen because recombination mechanisms appear to differ between his-3 and am, and because crossing over adjacent to his-5, like his-3, is regulated by...

Topics

Alleles
Chromosomes, Fungal
Crossing Over, Genetic
Fungal Proteins
Gene Conversion
Genetic Loci
Green Fluorescent Proteins
Hemizygote
Histones
Mutation
Neurospora crassa

Source

Open in PubMed Open full text

Identifiers

PMID: 22691725
DOI: 10.1016/j.fgb.2012.05.012
PMCID: PMC3402616

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

discussions

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics