Neurospora crassa str. 73 Assembly and Gene Annotation
About Neurospora crassa str. 73 (GCA_000786625)
Neurospora crassa is a type of red bread mold of the phylum
Ascomycota. The genus name, meaning
"nerve spore
" in Greek, refers to
the characteristic striations on the spores. The first published account
of this fungus was from an infestation of French bakeries in 1843.
N. crassa is used as a model organism because it is easy to grow and has a haploid life cycle that makes genetic analysis simple since recessive traits will show up in the offspring. Analysis of genetic recombination is facilitated by the ordered arrangement of the products of meiosis in Neurospora ascospores. Its entire genome of seven chromosomes has been sequenced.
Neurospora was used by Edward Tatum and George Wells Beadle in their
experiments for which they won the Nobel Prize in Physiology or Medicine
in 1958. Beadle and Tatum exposed N. crassa to x-rays, causing
mutations. They then observed failures in metabolic pathways caused by
errors in specific enzymes. This led them to propose the
"one gene, one
enzyme
" hypothesis that specific genes code for specific proteins.
Their hypothesis was later elaborated to enzyme pathways by Norman
Horowitz, also working on Neurospora. As Norman Horowitz reminisced in
2004,
"These experiments founded the science of what Beadle and Tatum
called 'biochemical genetics'. In actuality, they proved to be the
opening gun in what became molecular genetics and all developments that
have followed from that.
"
In the 24 April 2003 issue of Nature, the genome of N. crassa was reported as completely sequenced. The genome is about 43 megabases long and includes approximately 10,000 genes. There is a project underway to produce strains containing knockout mutants of every N. crassa gene.
In its natural environment, N. crassa lives mainly in tropical and sub-tropical regions. It can be found growing on dead plant matter after fires.
Neurospora is actively used in research around the world. It is important in the elucidation of molecular events involved in circadian rhythms, epigenetics and gene silencing, cell polarity, cell fusion, development, as well as many aspects of cell biology and biochemistry.
(Text and image from Wikipedia, the free encyclopaedia.)
Assembly
The assembly presented is the Neucr_trp3_1 assembly submitted to INSDC with the assembly accession GCA_000786625.1.
Annotation
The annotation presented is derived from annotation submitted to INSDC with the assembly accession GCA_000786625.1, with additional non-coding genes derived from Rfam. For more details, please visit INSDC annotation import.
More information
General information about this species can be found in Wikipedia.
Statistics
Summary
Assembly | Neucr_trp3_1, INSDC Assembly GCA_000786625.1, |
Database version | 113.1 |
Golden Path Length | 40,416,174 |
Genebuild by | DOE Joint Genome Institute |
Genebuild method | Import |
Data source | DOE Joint Genome Institute |
Gene counts
Coding genes | 11,650 |
Non coding genes | 390 |
Small non coding genes | 390 |
Pseudogenes | 8 |
Gene transcripts | 12,051 |