Inheritance and characterization of a dark-germinating, light-inhibited mutant in the fern Ceratopteris richardii

1991 ◽  
Vol 69 (12) ◽  
pp. 2616-2619 ◽  
Author(s):  
Rodney J. Scott ◽  
Leslie G. Hickok
Keyword(s):  
Genetic Analysis ◽  
Key Words ◽  
Nuclear Gene ◽  
Sexual Cycle ◽  
Wild Type ◽  
Ceratopteris Richardii ◽  
Mutant Selection ◽  
Light Inhibition ◽  
Selection For

Selection for a dark-germinating mutant was made with X-irradiated spores of Ceratopteris richardii. A single mutant line (HαDG1) was recovered and analyzed for its germination responses under different light–dark treatments and for transmission of the trait through a complete sexual cycle. HαDG1 was characterized by two phenotypes, dark germination and light inhibition of germination. These responses were exactly opposite from wild-type responses. The level of dark germination for a particular spore batch was stable through time, whereas light inhibition was unstable with time. Genetic analysis indicated that both phenotypes are associated with a single nuclear gene mutation that has been designated dkg1. Key words: fern, photomorphogenesis, mutant selection, germination, spore.

Biochemical and genetic characterization of a yeast TFIID mutant that alters transcription in vivo and DNA binding in vitro

1992 ◽  
Vol 12 (5) ◽  
pp. 2372-2382
Author(s):  
K M Arndt ◽  
S L Ricupero ◽  
D M Eisenmann ◽  
F Winston
Keyword(s):  
Amino Acid ◽  
Dna Binding ◽  
Direct Repeat ◽  
Single Amino Acid ◽  
Wild Type ◽  
Dna Binding Specificity ◽  
Selection For

A mutation in the gene that encodes Saccharomyces cerevisiae TFIID (SPT15), which was isolated in a selection for mutations that alter transcription in vivo, changes a single amino acid in a highly conserved region of the second direct repeat in TFIID. Among eight independent spt15 mutations, seven cause this same amino acid change, Leu-205 to Phe. The mutant TFIID protein (L205F) binds with greater affinity than that of wild-type TFIID to at least two nonconsensus TATA sites in vitro, showing that the mutant protein has altered DNA binding specificity. Site-directed mutations that change Leu-205 to five different amino acids cause five different phenotypes, demonstrating the importance of this amino acid in vivo. Virtually identical phenotypes were observed when the same amino acid changes were made at the analogous position, Leu-114, in the first repeat of TFIID. Analysis of these mutations and additional mutations in the most conserved regions of the repeats, in conjunction with our DNA binding results, suggests that these regions of the repeats play equivalent roles in TFIID function, possibly in TATA box recognition.

scholarly journals Genetic analysis of the Arabidopsis TIR1/AFB auxin receptors reveals both overlapping and specialized functions

eLife ◽  
2020 ◽  
Vol 9 ◽  
Author(s):  
Michael J Prigge ◽  
Matthieu Platre ◽  
Nikita Kadakia ◽  
Yi Zhang ◽  
Kathleen Greenham ◽  
...  
Keyword(s):  
Genetic Analysis ◽  
Early Embryo ◽  
Wild Type ◽  
The Family ◽  
Dependent Inhibition ◽  
Root Gravitropism ◽  
Specialized Function ◽  
Mutant Lines

The TIR1/AFB auxin co-receptors mediate diverse responses to the plant hormone auxin. The Arabidopsis genome encodes six TIR1/AFB proteins representing three of the four clades that were established prior to angiosperm radiation. To determine the role of these proteins in plant development we performed an extensive genetic analysis involving the generation and characterization of all possible multiply-mutant lines. We find that loss of all six TIR1/AFB proteins results in early embryo defects and eventually seed abortion, and yet a single wild-type allele of TIR1 or AFB2 is sufficient to support growth throughout development. Our analysis reveals extensive functional overlap between even the most distantly related TIR1/AFB genes except for AFB1. Surprisingly, AFB1 has a specialized function in rapid auxin-dependent inhibition of root growth and early phase of root gravitropism. This activity may be related to a difference in subcellular localization compared to the other members of the family.

ucFabV Requires Functional Reductase Activity to Confer Reduced Triclosan Susceptibility in Escherichia coli

2015 ◽  
Vol 25 (6) ◽  
pp. 394-402 ◽  
Author(s):  
Taylor L. Fischer ◽  
Robert J. White ◽  
Katherine F.K. Mares ◽  
Devin E. Molnau ◽  
Justin J. Donato
Keyword(s):  
Escherichia Coli ◽  
Reductase Activity ◽  
Acid Synthesis ◽  
Temperature Sensitive ◽  
Wild Type ◽  
E Coli ◽  
Enoyl Acp Reductase ◽  
Selection For

<b><i>Background/Aims:</i></b> We previously identified the Triclo1 fosmid in a functional metagenomic selection for clones that increased triclosan tolerance in <i>Escherichia coli</i>. The active enzyme encoded by Triclo1 is ucFabV. Although ucFabV is homologous to FabV from other organisms, ucFabV contains substitutions at key positions that would predict differences in substrate binding. Therefore, a detailed characterization of ucFabV was conducted to link its biochemical activity to its ability to confer reduced triclosan sensitivity. <b><i>Methods:</i></b> ucFabV and a catalytic mutant were purified and used to reduce crotonoyl-CoA in vitro. The mutant and wild-type enzymes were introduced into <i>E. coli</i>, and their ability to confer triclosan tolerance as well as suppress a temperature-sensitive mutant of FabI were measured. <b><i>Results:</i></b> Purified ucFabV, but not the mutant, reduced crotonoyl-CoA in vitro. The wild-type enzyme confers increased triclosan tolerance when introduced into <i>E. coli</i>, whereas the mutant remained susceptible to triclosan<i>. </i>Additionally, wild-type ucFabV, but not the mutant, functionally replaced FabI within living cells. <b><i>Conclusion:</i></b> ucFabV confers increased tolerance through its function as an enoyl-ACP reductase. Furthermore, ucFabV is capable of restoring viability in the presence of compromised FabI, suggesting ucFabV is likely facilitating an alternate step within fatty acid synthesis, bypassing FabI inhibition.

Characterization of mat A-2, mat A-3 and ΔmatA Mating-Type Mutants of Neurospora crassa

Genetics ◽  
1998 ◽  
Vol 148 (3) ◽  
pp. 1069-1079 ◽  
Author(s):  
Adlane V-B Ferreira ◽  
Zhiqiang An ◽  
Robert L Metzenberg ◽  
N Louise Glass
Keyword(s):  
Neurospora Crassa ◽  
Mating Type ◽  
Sexual Development ◽  
Vegetative Growth ◽  
Double Mutant ◽  
Sexual Cycle ◽  
Wild Type ◽  
Type Locus ◽  
Isolation And Characterization

AbstractThe mating-type locus of Neurospora crassa regulates mating identity and entry into the sexual cycle. The mat A idiomorph encodes three genes, mat A-1, mat A-2, and mat A-3. Mutations in mat A-1 result in strains that have lost mating identity and vegetative incompatibility with mat a strains. A strain containing mutations in both mat A-2 and mat A-3 is able to mate, but forms few ascospores. In this study, we describe the isolation and characterization of a mutant deleted for mat (ΔmatA), as well as mutants in either mat A-2 or mat A-3. The ΔmatA strain is morphologically wild type during vegetative growth, but it is sterile and heterokaryon compatible with both mat A and mat a strains. The mat A-2 and mat A-3 mutants are also normal during vegetative growth, mate as a mat A strain, and produce abundant biparental asci in crosses with mat a, and are thus indistinguishable from a wild-type mat A strain. These data and the fact that the mat A-2 mat A-3 double mutant makes few asci with ascospores indicate that MAT A-2 and MAT A-3 are redundant and may function in the same pathway. Analysis of the expression of two genes (sdv-1 and sdv-4) in the various mat mutants suggests that the mat A polypeptides function in concert to regulate the expression of some sexual development genes.

Microscopic Characterization of a Mutant Sperm Line of the Fern Ceratopteris Richardii

2001 ◽  
Vol 7 (S2) ◽  
pp. 456-457
Author(s):  
Kelly A. Davidson ◽  
Leslie G. Hickok ◽  
Karen S. Renzaglia
Keyword(s):  
Basal Bodies ◽  
Wild Type ◽  
Ceratopteris Richardii ◽  
Rhodamine Phalloidin ◽  
Transmission Electron ◽  
Inner Surface ◽  
Cell Organization ◽  
Light Fluorescence ◽  
Dapi Fluorescence

Mature sperm cells of Ceratopteris richardiiare spiraled over three revolutions and contain a locomotory apparatus with approximately 70 flagella attached at the cell anterior (Fig. 1). Abundant organelles are dispersed along the inner surface of an elongated, coiled nucleus (Figs. 1, 3, 8). The cytoskeleton comprises a network of microfilaments that encases the nucleus (Fig. 6) and two distinct microtubule arrays: a microtubular ribbon (spline) and flagella with anchoring basal bodies (Fig. 3). This study uses light, fluorescence, transmission electron (TEM), and scanning electron microscopy (SEM) to characterize cell organization in a motility impaired mutant sperm line of Ceratopteris.Because motility mutations likely involve the cytoskeleton, emphasis was placed on observing microtubule and actin arrays in the mutant compared to wild-type spermatozoids. Protocols follow Hoffman and Vaughn for TEM and Schmitt and Renzaglia for SEM. Microfilament arrays in relation to the nucleus were examined by rhodamine-phalloidin and DAPI fluorescence.

scholarly journals Biochemical and genetic characterization of a yeast TFIID mutant that alters transcription in vivo and DNA binding in vitro.

1992 ◽  
Vol 12 (5) ◽  
pp. 2372-2382 ◽  
Author(s):  
K M Arndt ◽  
S L Ricupero ◽  
D M Eisenmann ◽  
F Winston
Keyword(s):  
Amino Acid ◽  
Dna Binding ◽  
Direct Repeat ◽  
Single Amino Acid ◽  
Wild Type ◽  
Dna Binding Specificity ◽  
Selection For

A mutation in the gene that encodes Saccharomyces cerevisiae TFIID (SPT15), which was isolated in a selection for mutations that alter transcription in vivo, changes a single amino acid in a highly conserved region of the second direct repeat in TFIID. Among eight independent spt15 mutations, seven cause this same amino acid change, Leu-205 to Phe. The mutant TFIID protein (L205F) binds with greater affinity than that of wild-type TFIID to at least two nonconsensus TATA sites in vitro, showing that the mutant protein has altered DNA binding specificity. Site-directed mutations that change Leu-205 to five different amino acids cause five different phenotypes, demonstrating the importance of this amino acid in vivo. Virtually identical phenotypes were observed when the same amino acid changes were made at the analogous position, Leu-114, in the first repeat of TFIID. Analysis of these mutations and additional mutations in the most conserved regions of the repeats, in conjunction with our DNA binding results, suggests that these regions of the repeats play equivalent roles in TFIID function, possibly in TATA box recognition.

Nonsporulation in the Dutch elm disease fungus Ophiostoma ulmi: evidence for control by a single nuclear gene

1994 ◽  
Vol 72 (4) ◽  
pp. 461-467 ◽  
Author(s):  
Wayne C. Richards
Keyword(s):  
Key Words ◽  
Genetic Control ◽  
Genetic Stability ◽  
Nuclear Gene ◽  
Dutch Elm Disease ◽  
Wild Type ◽  
Ulmus Americana ◽  
Disease Symptoms ◽  
Ophiostoma Ulmi ◽  
Yeast Phase

A single nuclear gene controls nonsporulation in a novel isolate of the Dutch elm disease fungus Ophiostoma ulmi (Buism.) Nannf. This has been clearly demonstrated through segregation of the nonsporulating phenotype-in meiotic products recovered from crosses between a mutant nonsporulating isolate (WRB2-1) and wild-type sporulating isolates, between F1 progeny and their parents, and between F1 progeny. All crosses between nonsporulating and sporulating isolates yielded a 1:1 ratio for these two phenotypes in the meiotic products, whereas all crossings between isolates of the same phenotype produced meiotic products of that phenotype. The genetic stability of the nonsporulating phenotype was clearly shown when no disease symptoms were observed following artificial inoculation of the nonsporulating progeny into white elm, Ulmus americana L. Exposure to trifluoperazine, a calmodulin inhibitor, did not shift the nonsporulating isolates to the yeast phase, which supports our findings that nonsporulation is under genetic control rather than metabolic control. Key words: nonsporulation, Ophiostoma ulmi, mutant, single nuclear gene, meiotic products.

scholarly journals ISOLATION AND CHARACTERIZATION OF LIGHT-INSENSITIVE MUTANTS OF NEUROSPORA CRASSA

Genetics ◽  
1983 ◽  
Vol 104 (1) ◽  
pp. 11-21
Author(s):  
John Paietta ◽  
Malcolm L Sargent
Keyword(s):  
Genetic Analysis ◽  
Neurospora Crassa ◽  
Blue Light ◽  
Light Sensitivity ◽  
Phase Shifting ◽  
Nuclear Genes ◽  
Wild Type ◽  
Linkage Groups ◽  
Isolation And Characterization

ABSTRACT As part of a genetic analysis of blue light photoreception in Neurospora, three mutants were isolated that do not exhibit photosuppression of circadian conidiation, i.e., they show periodic conidiation in constant light. The mutations have been given the designations lis-1, lis-2 and lis-3 ("light insensitive"). The three mutations segregate as single nuclear genes, are nonallelic and are recessive to wild type in heterokaryon tests. The linkage groups of the mutations are as follows: lis-1, I; lis-2, VI; and lis-3, V. The light -insensitive phenotype of the mutants is restricted to the photosuppression response; other responses such as photoinduced phase shifting of the conidiation rhythm and photoinduced carotenogenesis are not altered. The physiological or biochemical defects of the mutants have not been established, but they are not similar to previous reported cases (i.e., rib and poky) in which a reduction in light sensitivity has been observed.

Genetic analysis of developmental mechanisms in Hydra. IV. Characterization of a nematocyst-deficient strain

1978 ◽  
Vol 30 (1) ◽  
pp. 175-185 ◽  
Author(s):  
T. Fujisawa ◽  
T. Sugiyama
Keyword(s):  
Genetic Analysis ◽  
Normal Level ◽  
The Body ◽  
Normal Rate ◽  
Wild Type ◽  
Head Region ◽  
Developmental Defects ◽  
Developmental Mechanisms ◽  
Body Column

The authors have previously found that mutant hydra strains showing various types of developmental defects can be isolated through sexual inbreeding of wild hydra. One such defective strain, called nem-4, contains virtually no stenoteles, one of the four types of nematocysts present in hydra, in its tentacles. However, stenoteles are present at a normal level in the body column of this strain, and they are turned over also at a normal rate. Grafting experiments between the head region of nem-4 hydra and the body column of wild type hydra (and vice versa) showed that wild type stenotele nematocytes can move into nem-4 tentacles but that nem-4 stenotele nematocytes can not move into the wild type tentacles. These observations suggest that the stenotele nematocytes are produced normally by differentiation from the interstitial cells in the body column of nem-4 hydra, but that they are somehow prevented from migrating into the tentacles in this strain.

GENETIC ANALYSIS OF EGG CANNIBALISM AND OVIPOSITION SITES FOR TRIBOLIUM CASTANEUM

1977 ◽  
Vol 19 (1) ◽  
pp. 119-124 ◽  
Author(s):  
DuWayne C. Englert ◽  
Don W. Raibley
Keyword(s):  
Genetic Analysis ◽  
Tribolium Castaneum ◽  
Oviposition Site ◽  
Wild Type ◽  
Preferential Selection ◽  
Egg Cannibalism ◽  
Behavioral Activities ◽  
Selection For ◽  
Oviposition Sites

The roles of cannibalism site, oviposition site and adult distribution in producing differences in the egg cannibalism rates for adults of the wild-type and antennapedia strains of Tribolium castaneum were investigated. The effect of egg genotype (+ or ap) in contributing a preferential selection for eating was also examined. The ap adults cannibalized eggs at a lower rate than did + adults, particularly when presented + eggs; no preference was noted for the + strain. Geographic centers for cannibalism site, oviposition site and adult distribution did not differ significantly. However, uniformity of cannibalistic activity and adult distribution occurred only for the + adults, suggesting that the behavioral activities of the two strains contributed to the differences of egg cannibalism possibly through a difference in searching capabilities.

Sign in / Sign up

Export Citation Format

Share Document