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The G alpha i homologue gna-1 controls multiple differentiation pathways in Neurospora crassa. 总被引:1,自引:0,他引:1
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Heterotrimeric G proteins are components of principal signaling pathways in eukaryotes. In higher organisms, alpha subunits of G proteins have been divided into four families, Gi, Gs, Gq, and G12. We previously identified a G alpha i homologue gna-1 in the filamentous fungus Neurospora crassa. Now we report that deletion of gna-1 leads to multiple phenotypes during the vegetative and sexual cycles in N. crassa. On solid medium, delta gna-1 strains have a slower rate of hyphal apical extension than wild type, a rate that is more pronounced under hyperosmotic conditions or in the presence of a cellophane overlay. delta gna-1 mutants accumulate less mass than wild-type strains, and their mass accumulation is not affected in the same way by exposure to light. delta gna-1 strains are defective in macroconidiation, possessing aerial hyphae that are shorter, contain abnormal swellings, and differentiate adherent macroconidia. During the sexual cycle, delta gna-1 strains are fertile as males. However, the mutants are female-sterile, producing small, aberrant female reproductive structures. After fertilization, delta gna-1 female structures do not enlarge and develop normally, and no sexual spores are produced. Thus, mutation of gna-1 results in sex-specific loss of fertility. 相似文献
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Cells of Bacillus firmus OF4 and Bacillus alcalophilus were examined by rapid-freeze freeze-fracture and freeze-substitution electron microscopy. No special vesicular structures linked to growth at alkaline pH were found, either within or associated with the cytoplasmic membrane. The cytoplasmic membranes of the alkaliphilic bacilli and the neutrophilic Bacillus subtilis BD99 were indistinguishable. Distinctive intramembrane particle rings, presumed to be flagellar structures on the basis of distribution and morphological characteristics, were found in all of these species. These observations indicate that the adaptations required to effect oxidative phosphorylation and flagellar rotation at extreme alkaline pH occur without gross morphological rearrangement. 相似文献
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Large numbers of Pneumocystis carinii (2 X 10(10) nuclei) were isolated and separated from the lungs of immunosuppressed rats by an enzymatic (collagenase, hyaluronidase and DNase) digestion procedure. The nucleic acid isolated from this P. carinii-enriched preparation was characterized by melting point analysis and RNA-sizing gels. The GC content of P. carinii DNA was approximately 33% while the rat DNA was 41.4%. In addition, RNA isolated from the P. carinii-enriched preparation showed unique ribosomal RNA bands of 3.4 kb and 1.8 kb as compared with uninfected rat lung ribosomal RNA which banded at 4.8 and 1.9 kb. Following isolation and fragmentation by sonication, the P. carinii DNA fragments were inserted into the vector, lambda gt-11. The resultant library contained 1.1 X 10(5) phage, of which 40-45% hybridized to P. carinii DNA but not to rat DNA. 相似文献
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J. Timothy Fulenwider Bernard M. Nordlinger Bajhat A. Faraj George L. Ivey Daniel Rudman 《The Yale journal of biology and medicine》1978,51(6):625-633
In normal individuals, the main route for tyrosine degradation is the hepatic pathway tyrosine→4-hydroxyphenylpyruvic acid→homogentisic acid→CO2. Quantitatively minor pathways, in large part extrahepatic, are: tyrosine→tyramine→octopamine and tyrosine→dopa→catecholamines.In cirrhosis, the main hepatic pathway is blocked to varying degrees at the first three stages. This appears to be due to lack of activity of the enzymes tyrosine transaminase, PHPA oxidase, and HGA oxidase, the first step being rate limiting. Hypertyrosinemia and tyrosine intolerance result.With the main hepatic pathway partially blocked, an abnormally large amount of tyrosine passes into the normally minor extrahepatic pathway leading to the false neurotransmitters tyramine and octopamine. Overproduction of these amines ensues and they accumulate in the body fluid.The false neurotransmitters can displace catecholamines from their storage sites in the peripheral and central nervous system, and thereby disrupt adrenergic processes in arterioles, kidneys, and brain. Their accumulation in cirrhotic patients may play a role in the pathogenesis of hepatic encephalopathy, hepatorenal syndrome, and hyperdynamic circulation. 相似文献
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Rosloniec EF Ivey RA Whittington KB Kang AH Park HW 《Journal of immunology (Baltimore, Md. : 1950)》2006,177(6):3884-3892
The expression of HLA-DR1 (DRB1*0101) is associated with an enhanced risk for developing rheumatoid arthritis (RA). To study its function, we have solved the three-dimensional structure of HLA-DR1 complexed with a candidate RA autoantigen, the human type II collagen peptide CII (259-273). Based on these structural data, the CII peptide is anchored by Phe263 at the P1 position and Glu266 at P4. Surprisingly, the Lys at the P2 position appears to play a dual role by participating in peptide binding via interactions with DRB1-His81 and Asn82, and TCR interaction, based on functional assays. The CII peptide is also anchored by the P4 Glu266 residue through an ionic interaction with DRB1-Arg71 and Glu28. Participation of DRB1-Arg71 is significant because it is part of the shared epitope expressed by DR alleles associated with RA susceptibility. Potential anchor residues at P6 and P9 of the CII peptide are both Gly, and the lack of side chains at these positions appears to result in both a narrower binding groove with the peptide protruding out of the groove at this end of the DR1 molecule. From the TCR perspective, the P2-Lys264, P5-Arg267, and P8-Lys270 residues are all oriented away from the binding groove and collectively represent a positive charged interface for CII-specific TCR binding. Comparison of the DR1-CII structure to a DR1-hemagglutinin peptide structure revealed that the binding of these two peptides generates significantly different interfaces for the interaction with their respective Ag-specific TCRs. 相似文献
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J. J. Le Roux S. Geerts P. Ivey S. Krauss D. M. Richardson J. Suda J. R. U. Wilson 《Biological invasions》2010,12(12):3989-4002
Most legislation pertaining to non-native organisms is implicitly focussed at the individual species level. However, in some
cases interspecific hybrids can be more invasive than any of the parent species. This is problematic for policy makers, and
for horticulturists developing or trading in new ornamental cultivars. We explore these issues in the context of the need
to manage naturalized populations of Kangaroo Paws (Anigozanthos species) in South Africa. Self-sustaining, dense populations of naturalized Kangaroo Paws occur at several localities and
are highly attractive to local nectar-feeding birds. The populations show high levels of seed set with or without bird pollination.
Given the known propensity of Kangaroo Paws to hybridise in their native range in Australia, and confusion about the species
identity of naturalized populations in South Africa, it was essential to resolve some key taxonomic issues in the group. We
constructed the first molecular phylogeny for all species of the Kangaroo Paw group (genera Anigozanthos and Macropidia; family Haemodoraceae). As previously determined by taxonomists working on herbarium specimens, naturalized populations were
identified as A. flavidus. In addition, we also identified a second species, A. rufus. Relative genome size estimates for Anigozanthos species indicated that small inter-specific differences in genome sizes are positively correlated to hybrid fitness. Anigozanthos flavidus and A. rufus have relatively ‘compatible’ genomes and may produce fertile hybrids under field conditions. However, for species whose genome
size differ more than ~30%, there is little inter-specific compatibility and consequently a very low risk of producing fertile
hybrids. In conclusion, we recommend that trade in Kangaroo Paws in South Africa should be temporarily restricted and that
particular cultivars should first be subjected to a careful risk assessment. 相似文献