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Example sentences for: neurospora
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Species abbreviations used in this paper are as follows: AcNV, Autographa californica nucleopolyhedrosis virus; AgNV, Anticarsia gemmatalis nucleopolyhedrosis virus; AMV, Amsacta moorei entomopoxvirus; BPBK5T, Lactococcus phage BK5-T; BmNV, Bombyx mori nuclear polyhedrosis virus; BP933W, bacteriophage 933W; BPA118, bacteriophage A118; BPAPSE1, bacteriophage APSE1; BPbIL285, bacteriophage bIL285; BPbIL286, bacteriophage bIL286; BPbIL309, bacteriophage bIL309; BPD3, bacteriophage D3; BPφ80, bacteriophage φ80; BPHK620, bacteriophage HK620; BPHK97, bacteriophage HK97; BPLLH, bacteriophage LLH; BPMx8, bacteriophage Mx8; BPN15, bacteriophage N15; BPP1, bacteriophage P1; BPP22, bacteriophage P22; BPP4, bacteriophage P4; BPP27, bacteriophage P27; BPφPV, bacteriophage φPV; BPR1T, bacteriophage R1T; BPSpβC2, bacteriophage SpβC2; BPT5, bacteriophage T5; BPVT2-Sa, bacteriophage VT2; Cab, Clostridium acetobutylicum ; Cal, Candida albicans ; CIV, Chilo iridescent virus; CnBV, Culex nigripalpus baculovirus; CpGV, Cydia pomonella granulovirus; DpAV4, Diadromus pulchellus ascovirus; Ec, Escherichia coli ; EpNV, Epiphyas postvittana nucleopolyhedrovirus; EV, ectromelia virus; Eni, Emericella nidulans ; ESV, Ectocarpus siliculosus virus; FPV, fowlpox virus; HaEPV, Heliothis armigera entomopoxvirus; HaNV, Heliocoverpa armigera nucleopolyhedrovirus G4; HK97, bacteriophage HK97; HzNV, Helicoverpa zea single nucleocapsid nucleopolyhedrovirus; Kla, Kluyveromyces lactis ; LcBPA2, Lactobacillus casei bacteriophage A2; LdNV, Lymantria dispar nucleopolyhedrovirus; LsNV, Leucania separata nuclear polyhedrosis virus; MbNV, Mamestra brassicae nucleopolyhedrovirus; MSV, Melanoplus sanguinipes entomopoxvirus; Nc, Neurospora crassa ; Nm, Neisseria meningitidis ; OpNV, Orgyia pseudotsugata single capsid nuclear polyhedrosis virus; Pa, Pseudomonas aeruginosa ; PxGV, Plutella xylostella granulovirus; Sa,
Mammalian protein phosphatase 5 (PP5) and its homolog protein phosphatase T1 (Ppt1p) from the yeast Saccharomyces cerevisiae contain a catalytic domain structurally related to the catalytic subunits of PP1, PP2A and PP2B, and an N-terminal domain consisting of multiple tetratricopeptide repeats (TPRs) not found in other members of this family of phosphatases [ 1 2 3 ] . Homologs have also been identified in Xenopus laevis [ 4 ] , Neurospora crassa [ 5 ] , Drosophila melanogaster [ 6 ] , Trypanosoma brucei [ 7 ] , Plasmodium falciparum [ 8 9 ] , and cauliflower [ 10 ] , and homologs for Caenorhabditis elegans, Schizosaccharomyces pombe and Arabidopsis thaliana are predicted (accession number CAB60937, CAA17690 and AAD21727, respectively).
Neurospora
In particular, a series of nested deletions of the P6 stem-loop have been shown to partially or completely compromise ribozyme activity [ 15 ] . More importantly, either magnesium or the tyrosyl tRNA synthetase from Neurospora mitochondria (CYT18) can suppress many of these defects [ 16 17 ] . Previous studies with other introns have also revealed that deletion of the P5 stem-loop can modulate ribozyme activity [ 18 19 ] . We hypothesized that sites where deletions modulated ribozyme activity might also prove to be sites where aptamer conformational changes would modulate ribozyme activity.
Molecular-genetic analysis of circadian rhythms in Drosophila, Neurospora and more recently in vertebrate systems has led to the conclusion [ 3, 4, 5] that rhythms of gene expression are of central importance both in the sustained generation of rhythmicity (clock genes) and in the control of output pathways (clock controlled genes).
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