Characterization of ard B and ard C actin gene loci of Physarum polycephalum

Summary Physarum polycephalum (strain M₃CVIII) contains four unlinked actin gene loci, each with two alleles (ard A1, ard A2, ard B1, ard B2, ard C1, ard C2, ard D1 and ard D2). The 4.8 kbp HindIII component of the ard C2 locus was isolated as a recombinant phage-, after HindIII fragments of Physarum DNA ranging from 4.3 kbp to 5.5 kbp were cloned into phage- NM1149. The fraction of Physarum DNA cloned contained the ard C locus, and no other actin locus. Small inserts were favoured to reduce the probability of cloning a complete repetitive element, because such elements have been found to adversely affect the stability of recombinants.The coding sequences of the actin gene (approximately 1.1 kbp) spanned more than 3 kbp indicating the presence of introns. A 1.6 kbp HindIII/EcoRI fragment of the ard C locus, which contained some coding sequences, hybridized extensively with HindIII fragments of genomic DNA indicating the presence of repetitive sequences. A 2.3 kbp HindIII/EcoRI fragment containing most of the coding sequences of the C2 allele of the ard C locus hybridized with the C1, allele and both alleles of the ard B locus, but not with the ard A locus or ard D locus. This distinction was used to establish for the ard B and ard C loci the relationship between the EcoRI and HindIII fragments that define an ard locus. The ability to distinguish between ard loci may facilitate studies of the expression of particular actin loci.     

Studies of partially repressed mutants at the tamA and areA loci in Aspergillus nidulans

Summary Mutants, designated tamA^r, have been isolated on the basis of simultaneous resistance to toxic analogues thiourea, aspartate hydroxamate and chlorate with L-alanine as the sole nitrogen source. tamA^r mutants are also resistant to methylammonium. This resistance of tamA^r mutants is correlated with partially repressed activity of a number of enzyme and transport systems regulated by ammonium. Furthermore, tamA^r mutants have low NADP-glutamate dehydrogenase (NADP-GDH) activity and also efflux ammonium under certain growth conditions.Mutants at the areA locus (areA^r) have also been isolated on the basis of resistance to these analogues, with nitrate or L-aspartate as the nitrogen source. These, similar to tamA^r lesions, result in resistance to methylammonium and are partially repressed for ammonium repressible systems, but in contrast to tamA^r, areA^r alleles have wild-type NADP-GDH activity and normal ammonium efflux.tamA^r and areA^r mutants grow as wild type on all nitrogen or carbon sources tested, are recessive, and appear to be epistatic to all other mutations (gdhA1, meaA8 and meaB6) which result in derepressed levels of ammonium regulated system. Whereas tamA^r and areA^r phenotypes are additive, tamA^r is epistatic to areA^d phenotype.     

Autonomy of the wingless mutation in Drosophila melanogaster

Summary T(Y;2) translocations were used to cytologically localise the wingless locus of Drosophila melanogaster. We found that an existing T(Y;2), which is an insertion of a segment of 2L into the Y chromosome, has wg ⁺ within this insert. This Y chromosome was used to generate an attached XY chromosome containing wg ⁺. The mutation claret-nondisjunctional (ca ^nd) was used to induce the loss of this XY chromosome and thus generate gynandromorphs with wg ¹/wg ¹ male tissue and wg ⁺/wg ¹/wg ¹ female tissue. Analysis of these gynanders demonstrated that a genotypically wingless mutant hemithorax is usually also phenotypically mutant in these half body mosaics; thus wg ¹ is discautonomous. This observation is of interest as it is known that wg is not cell autonomous.     

The mutation ofEscherichia coli to resistance to bacteriophages Tl and Tls

Summary The number of phage-resistant mutants in unirradiated and in ultraviolet-irradiated cultures ofE. coli strains B and B/r is usually greater when the selecting agent is Tls. It is shown that this cannot be explained by a) completely independent gene changes, b) the presence of host range phage mutants or c) new mutations due to prolonged survival of wild type bacteria in the prescence of phage. Evidence is presented which indicates that the difference in selection by Tl and Tls may be explained satisfactorily by the presence of incompletely expressed bacterial mutants in the cultures before plating. This constitutes indirect evidence for a phenotypic lag. It is shown further that the development of resistance to Tls probably precedes the development of full resistance to both phages.The appearance of new ultraviolet-induced mutations, selected by Tls, is found to fulfill expectations based on the existence of such a phenotypic lag.

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Zusammenfassung Die Anzahl der phagenresistenten Mutanten in unbestrahlten und UV-bestrahlten Kulturen derE. coli Stämme B und B/r ist im allgemeinen größer, wenn die Selektion mit Tls durchgeführt wird. Dieses kann nicht erklärt werden durch a) vollständig unabhängige Genveränderungen, b) die Gegenwart von hostrange Phagenmutanten, oder c) neue Mutationen bedingt durch längeres Überleben von Wildtypus-Bakterien in der Gegenwart von Phagen. Es wird gezeigt, daß der Unterschied in der Selektion von Tl und Tls ausreichend erklärt werden kann durch die Gegenwart von unvollständig manifestierten Bakterienmutanten, die vor dem plating in den Kulturen vorhanden sind. Dieses bildet indirekten Beweis für eine phänotypische Lagphase. Es wird weiterhin gezeigt, daß die Entwicklung der Resistenz gegenüber Tls wahrscheinlich der Entwicklung von Vollresistenz gegenüber beiden Phagen vorangeht.Das Auftreten von neuen UV-induzierten, durch Tls selektierten Mutanten stimmt mit dem Vorhandensein einer derartigen phänotypischen Lagphase überein.

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With 6 Figures in the text.     

Comparison between rDNA magnification and bb lethal mutation frequencies in Drosophila melanogaster

Summary Unequal mitotic sister strand crossing over has been evoked to explain the occurrence of phenotypically bb^- males in the progeny of phenotypically bobbed males during magnification. If this is the case, complementary bb¹ loci should be obtained together with the bb¹. To test this hypothesis we compared the frequency of bb lethal mutations in the sperms of bb males with the percentage of phenotypically bb⁺ males obtained during magnification of these bb males. We then compared these values with those occurring in phenotypically bb⁺ control males. We found that, while the number of bb⁺ males obtained during magnification, though variable, is high, the bb lethal mutation occurs at a very low frequency in all the genetic conditions, whatever the phenotype of the parental male.     

Frequencies of mutagen-induced coincident mitotic recombination at unlinked loci in Saccharomyces cerevisiae

Frequencies of coincident genetic events were measured in strain D7 of Saccharomyces cerevisiae. This diploid strain permits the detection of mitotic gene conversion involving the trp5-12 and trp5-27 alleles, mitotic crossing-over and gene conversion leading to the expression of the ade2-40 and ade2-119 alleles as red and pink colonies, and reversion of the ilv1-92 allele. The three genes are on different chromosomes, and one might expect that coincident (simultaneous) genetic alterations at two loci would occur at frequencies predicted by those of the single alterations acting as independent events. Contrary to this expectation, we observed that ade2 recombinants induced by bleomycin, beta-propiolactone, and ultraviolet radiation occur more frequently among trp5 convertants than among total colonies. This excess among trp5 recombinants indicates that double recombinants are more common than expected for independent events. No similar enrichment was found among Ilv(+) revertants. The possibility of an artifact in which haploid yeasts that mimic mitotic recombinants are generated by a low frequency of cryptic meiosis has been excluded. Several hypotheses that can explain the elevated incidence of coincident mitotic recombination have been evaluated, but the cause remains uncertain. Most evidence suggests that the excess is ascribable to a subset of the population being in a recombination-prone state.     

Environmentally constrained mutation and adaptive evolution in Salmonella

The relationship between environment and mutation is complex [1]. Claims of Lamarkian mutation [2] have proved unfounded [3], [4] and [5]; it is apparent, however, that the external environment can influence the generation of heritable variation, through either direct effects on DNA sequence [6] or DNA maintenance and copying mechanisms [7], [8], [9] and [10], or as a consequence of evolutionary processes [11], [12], [13], [14], [15] and [16]. The spectrum of mutational events subject to environmental influence is unknown [6] and precisely how environmental signals modulate mutation is unclear. Evidence from bacteria suggests that a transient recombination-dependent hypermutational state can be induced by starvation [5]. It is also apparent that chnages in the mutability of specific loci can be influenced by alterations in DNA topology [10] and [17]. Here we describe a remarkable instance of adaptive evolution in Salmonella which is caused by a mutation that occurs in intermediate-strength osmotic environments. We show that the mutation is not ‘directed’ and describe its genetic basis. We also present compelling evidence in support of the hypothesis that the mutational event is constrained by signals transmitted from the external environment via changes in the activity of DNA gyrase.     

Improving Salmonella vector with rec mutation to stabilize the DNA cargoes

Background  

Salmonella has been employed to deliver therapeutic molecules against cancer and infectious diseases. As the carrier for target gene(s), the cargo plasmid should be stable in the bacterial vector. Plasmid recombination has been reduced in E. coli by mutating several genes including the recA, recE, recF and recJ. However, to our knowledge, there have been no published studies of the effect of these or any other genes that play a role in plasmid recombination in Salmonella enterica.     

Characterization of the cyrl-2 UGA mutation in Saccharomyces cerevisiae

Summary cyrl-2 is a temperature-sensitive mutation of the yeast adenylate cyclase structural gene, CYR1. The cyrl-2 mutation has been suggested to be a UGA mutation since a UGA suppressor SUP201 has been isolated as a suppressor of the cyrl-2 mutation. Construction of chimeric genes restricted the region containing the cyrl-2 mutation, and the cyrl-2 UGA mutation was identified at codon 1282, which lies upstream of the region coding for the catalytic domain of adenylate cyclase. Alterations in the region upstream of the cyrl-2 mutation site result in null mutations. The complete open reading frame of the cyrl-2 gene expressed under the control of the GAL1 promoter complemented cyrl-dl in a galactose-dependent manner. These results suggest that at the permissive temperature weak readthrough occurs at the cyrl-2 mutation site to produce low levels of active adenylate cyclase. An endogenous suppressor in yeast cells is assumed to be responsible for this readthrough.     

A dominant interfering mutation in RAS1 of Saccharomyces cerevisiae

A mutant allele of RAS1 that dominantly interferes with the wild-type Ras function in the yeast Saccharomyces cerevisiae was discovered during screening of mutants that suppress an ira2 disruption mutation. A single amino acid substitution, serine for glycine at position 22, was found to cause the mutant phenotype. The inhibitory effect of the RAS1 ^Ser22 gene could be overcome either by overexpression of CDC25 or by the ira2 disruption mutation. These results suggest that the RAS1^Ser22 gene product interferes with the normal interaction of Ras with Cdc25 by forming a dead-end complex between Ras1^Ser22 and Cdc25 proteins.     

A mutation, bsu, that suppresses temperature-sensitive dnaB function in Escherichia coli K12

Summary A mutation of Escherichia coli K12 that suppresses certain temperature-sensitive dnaB mutations was identified. The suppressor, named bsu maps very near the dnaG mutations. The bsu mutation in dnaB bacteria appears to be dominant over the wildtype allele, and suppresses specifically the temperature-sensitive dnaB mutations which are revertible phenotypically when salt is present. The observed specificity in suppression suggests that the product of bsu alone cannot substitute for the defective dnaB gene products. These findings suggest stronly that gene products of bsu and dnaB interact with each other in the process of DNA replication in E. coli.     

Nucleotide sequence of a recA operator mutation

Summary A single base pair change (AT to GC) is shown to be responsible for derepression of recA. The mutation (recAo281) alters the binding sequence for the LEXA repressor.Abbreviations bp base pair - kb kilobase pair     

Effect of the apterous 56f mutation on N -acetyltransferase and alkaline phosphatase activities in Drosophila melanogaster females

Alkaline phosphatase (AP) and N-acetyltransferase (NAT) activities were studied in 1-day-old Drosophila melanogaster females of the apterous ^56f (ap ^56f ) strain, having an decreased level of the juvenile hormone (JH) and a increased level of dopamine as a result of the mutation, and in the Canton S ancestral wild-type strain in the normal conditions and upon an experimental increase in JH titer. The AP and NAT activities in ap ^56f females were significantly lower than in Canton S females in the norm. JH application increased the AP activity of mutant females to the level characteristic to JH-treated wild-type females. Original Russian Text ? E.V. Bogomolova, N.V. Adonyeva, N.E. Gruntenko, I.Yu. Rauschenbach, 2008, published in Genetika, 2008, Vol. 44, No. 5, pp. 710–712.