TEMPERATURE-SENSITIVE MUTATIONS IN DROSOPHILA MELANOGASTER. XVI. THE GENETIC PROPERTIES OF SEX-LINKED RECESSIVE COLD-SENSITIVE MUTANTS

1973 ◽  
Vol 15 (2) ◽  
pp. 237-254 ◽  
Author(s):  
Helen Mayoh ◽  
David T. Suzuki
Keyword(s):  
Drosophila Melanogaster ◽  
Ribosomal Protein ◽  
Cold Sensitivity ◽  
Female Sterility ◽  
Temperature Sensitive ◽  
X Chromosomes ◽  
Cold Sensitive ◽  
The Right ◽  
Minute Mutations

Among 3,919 EMS-treated X chromosomes, 25 were retained as cold-sensitive (cs) lethals. That is, more than 20% of flies carrying a cs lethal survive at 22 °C and none at 17 °C and for cs semi-lethals, >30% at 22 °C and <13% at 17 °C. The cs mutations are not randomly distributed, seven being located at the X tip and three being alleles to the right of car. Over half exhibited female sterility or reduced fertility and seven exhibited visible phenotypes characteristic of bobbed and Minute mutations. The possible enrichment for ribosomal protein defects by screening for cold-sensitivity is discussed.

scholarly journals TEMPERATURE-SENSITIVE MUTATIONS IN DROSOPHILA MELANOGASTER. XVII. HEAT- AND COLD-SENSITIVE LETHALS ON CHROMOSOME 3

Genetics ◽  
1973 ◽  
Vol 74 (3) ◽  
pp. 509-520
Author(s):  
S Elaine Tasaka ◽  
David T Suzuki
Keyword(s):  
Drosophila Melanogaster ◽  
Ethyl Methanesulfonate ◽  
Cold Sensitivity ◽  
Chromosome 3 ◽  
Temperature Sensitive ◽  
Single Mutation ◽  
Physical Length ◽  
Lethal Mutations ◽  
Genetic Length ◽  
Cold Sensitive

ABSTRACT Ethyl methanesulfonate-treated third chromosome of Drosophila melanogaster were tested for the presence of dominant and recessive temperature-sensitive lethal mutations at 17°, 22° and 29°C. Out of 1,176 chromosomes tested, no dominant ts lethals, 21 heat-sensitive, 22 cold-sensitive and 10 heat-cold-sensitive lethals were recovered. Heat-cold sensitivity was produced by a single mutation in all cases. Sixty-two percent of the ts lethals were fertile as homozygotes in both sexes. Surprisingly, 88% of the ts lethals mapped between st and Sb, a region straddling the centromere and estimated to comprise 12.9% of the genetic length and 55% of the physical length of chromosome 3. All but one of the heat- and cold-sensitive lethals complemented with each other at their respective restrictive temperatures.

scholarly journals A COLD-SENSITIVE ZYGOTIC LETHAL CAUSING HIGH FREQUENCIES OF NONDISJUNCTION DURING MEIOSIS I IN DROSOPHILA MELANOGASTER FEMALES

Genetics ◽  
1974 ◽  
Vol 76 (3) ◽  
pp. 511-536
Author(s):  
Theodore R F Wright
Keyword(s):  
Drosophila Melanogaster ◽  
Sensitive Period ◽  
Temperature Sensitive ◽  
Large Array ◽  
X Chromosomes ◽  
High Frequencies ◽  
Cold Sensitive ◽  
Pupal Mortality ◽  
Mortality Analysis ◽  
Meiosis I

ABSTRACT The X-linked, cold-sensitive zygotic lethal, l(1)TW-6cs, both in homozygous and heterozygous females, induces nondisjunction of all four chromosomes at Meiosis I at both 25° and 17°. Nondisjunction frequencies approaching 0.5 for the X and fourth chromosomes have been observed at 16°–18°. The disjunction of the X chromosomes in males is not affected. The mutant causes mitotic irregularities in zygotes at both 25° and 17°. Mortality of all zygotes produced by the crosses 6cs/6cs × 6cs/BsY and FM7/6cs × 6cs/BsY is respectively 86% and 67–74% at 25° and 99.8–99.9% and 94% at 17°. The mortality of 6cs hemizygotes derived from females carrying no doses of 6cs (C(1)DX,y f/y × 6cs/BsY) is 45–55% at 25° and 98% at 17°. The length of the temperature-sensitive period for 6cs homo- and hemizygotes is affected by the maternal dosage of 6cs; the shortest TSP is for zero and the longest is for two maternal doses. Mortality takes place primarily during embryogenesis with some larval and little pupal mortality. Analysis of sectioned embryos indicates that the large array of different patterns of damage observed could have arisen from abnormal cleavage divisions and the incomplete population of the blastoderm with nuclei.

Studies on the female-sterile phenotype of 1(1)su(f) ts76a, a temperature-sensitive allele of the suppressor of forked mutation in Drosophila melanogaster

Development ◽  
1980 ◽  
Vol 55 (1) ◽  
pp. 247-256
Author(s):  
Thomas G. Wilson
Keyword(s):  
Cell Death ◽  
Drosophila Melanogaster ◽  
Follicle Cell ◽  
Lethal Mutation ◽  
Female Sterility ◽  
Temperature Sensitive ◽  
Egg Chambers ◽  
A Cell ◽  
Sensitive Allele

A new allele of the suppressor of forked [su(f)] mutation in Drosophila melanogaster has been found and designated 1(1)su(f)ts76a. It is temperature-sensitive for suppression of forked (f) and has additional temperature-sensitive phenotypes of lethality, female sterility, and abnormal bristle formation at 29 °C. It closely resembles two other conditional alleles of su(f), 1(1)su(f)ts67g and 1(1)ts726. Female sterility at 29 °C is characterized by both disorganized egg chambers in the ovarioles and also chorion-deficient oocytes. Both of these abnormalities may be the result of premature follicle cell death. The observations on 1(1)su(f)ts76a are consistent with the proposal that the similar allele, 1(1)ts726, is a cell-lethal mutation specifically affecting mitotically active cells.

THE DEVELOPMENTAL GENETICS OF THE TEMPERATURE-SENSITIVE LETHAL ALLELE OF THE SUPPRESSOR OF FORKED, l(1)su(f)ts67g, IN DROSOPHILA MELANOGASTER

Genetics ◽  
1974 ◽  
Vol 76 (3) ◽  
pp. 487-510
Author(s):  
Marianne E Dudick ◽  
Theodore R F Wright ◽  
Lynda Lee Brothers
Keyword(s):  
Drosophila Melanogaster ◽  
Ribosomal Protein ◽  
Sensitive Period ◽  
Developmental Genetics ◽  
Temperature Sensitive ◽  
Wild Type Allele ◽  
Wild Type ◽  
Type Allele ◽  
Lethal Allele

ABSTRACT A temperature-sensitive lethal allele of suppressor of forked, l(1)su(f)ts67g (ts67), has been discovered and characterized as follows: Flies which are hemizygous for ts67 live at 18° and 25° but die at 30° primarily as larvae. The temperature-sensitive period for ts67 homozygotes or hemizygotes begins in second instar and ends at pupation. ts67 is lethal at 30° when heterozygous with suppressor of forked (su(f)), a deficiency for suppressor of forked (su(f)  -), and a non-conditional lethal allele of suppressor of forked (3DES). It is viable at 30° when heterozygous with the wild-type allele of suppressor of forked. At 25° but not at 18° forked bristles are suppressed in flies of the following genotypes: fsts67/Y, fsts67/fsts67, fsts67/fssu(f), futs67/fs3DES, futs67/fssu(f)  -, futs67/fssu(f). There is some suppression of forked bristles at 25° in the heterozygote, fsts67/fs+su(f). The forked bristle phenotype is not suppressed at either temperature in flies of the genotypes futs67/Y, futs67/futs67/ (fs and fu indicating suppressible and unsuppressible alleles of forked). The temperature-sensitive period for suppression of forked bristles begins at pupation and extends through the period of bristle synthesis. The deficiency phenotype (bristles reduced in size or absent, wing wrinkled or blistered, eyes rough) typical of flies of the genotype fssu(f)/fssu(f)  - at 18° and 25°, is exhibited by flies of the genotypes fsts67/fssu(f)  - at 25° and futs67/fssu(f) at 29°. An allele of lozenge (lz1) which can be suppressed by su(f) is suppressed at 25° but not at 18° in lz1ts67/Y males. ts67 homozygous females are fertile at 25° but sterile at 30°. The hypothesis is discussed that the su(f) locus codes for a ribosomal protein and that suppression and enhancement are affected by mutations at the locus by mutant ribosome-induced misreading. The possibility is presented that ts67 may be used to determine the translation time in development of any gene.

scholarly journals The lethal(1)TW-6cs mutation of Drosophila melanogaster is a dominant antimorphic allele of nod and is associated with a single base change in the putative ATP-binding domain.

Genetics ◽  
1991 ◽  
Vol 129 (2) ◽  
pp. 409-422 ◽  
Author(s):  
R S Rasooly ◽  
C M New ◽  
P Zhang ◽  
R S Hawley ◽  
B S Baker
Keyword(s):  
Drosophila Melanogaster ◽  
Chromosome Breakage ◽  
Base Change ◽  
Cold Sensitivity ◽  
Atp Binding ◽  
Loss Of Function ◽  
Single Base ◽  
Recessive Lethal Mutation ◽  
Cold Sensitive ◽  
Single Base Change

Abstract The l(1)TW-6cs mutation is a cold-sensitive recessive lethal mutation in Drosophila melanogaster, that affects both meiotic and mitotic chromosome segregation. We report the isolation of three revertants of this mutation. All three revert both the meiotic and mitotic effects as well as the cold sensitivity, demonstrating that all three phenotypes are due to a single lesion. We further show that these revertants fail to complement an amorphic allele of the nod (no distributive disjunction) locus, which encodes a kinesin-like protein. These experiments demonstrate that l(1)TW-6cs is an antimorphic allele of nod, and we rename it nodDTW. Sequencing of the nod locus on a nodDTW-bearing chromosome reveals a single base change in the putative ATP-binding region of the motor domain of nod. Recessive, loss-of-function mutations at the nod locus specifically disrupt the segregation of nonexchange chromosomes in female meiosis. We demonstrate that, at 23.5 degrees, the meiotic defects in nodDTW/+ females are similar to those observed in nod/nod females; that is, the segregation of nonexchange chromosomes is abnormal. However, in nodDTW/nodDTW females, or in nodDTW/+ females at 18 degrees, we observe a more severe meiotic defect that apparently affects the segregation of both exchange and nonexchange chromosomes. In addition, nodDTW homozygotes and hemizygous males have previously been shown to exhibit mitotic defects including somatic chromosome breakage and loss. We propose that the defective protein encoded by the nodDTW allele interferes with proper chromosome movement during both meiosis and mitosis, perhaps by binding irreversibly to microtubules.

A Mutation in a Methionine tRNA Gene Suppresses the prp2-1 Ts Mutation and Causes a Pre-mRNA Splicing Defect in Saccharomyces cerevisiae

Genetics ◽  
1999 ◽  
Vol 153 (3) ◽  
pp. 1105-1115
Author(s):  
Dong-Ho Kim ◽  
Gretchen Edwalds-Gilbert ◽  
Chengzhen Ren ◽  
Ren-Jang Lin
Keyword(s):  
Saccharomyces Cerevisiae ◽  
Trna Gene ◽  
Mrna Splicing ◽  
Cold Sensitivity ◽  
Temperature Sensitive ◽  
Growth Defects ◽  
Splicing Defect ◽  
Allele Specific ◽  
Cold Sensitive

Abstract The PRP2 gene in Saccharomyces cerevisiae encodes an RNA-dependent ATPase that activates spliceosomes for the first transesterification reaction in pre-mRNA splicing. We have identified a mutation in the elongation methionine tRNA gene EMT1 as a dominant, allele-specific suppressor of the temperature-sensitive prp2-1 mutation. The EMT1-201 mutant suppressed prp2-1 by relieving the splicing block at high temperature. Furthermore, EMT1-201 single mutant cells displayed pre-mRNA splicing and cold-sensitive growth defects at 18°. The mutation in EMT1-201 is located in the anticodon, changing CAT to CAG, which presumably allowed EMT1-201 suppressor tRNA to recognize CUG leucine codons instead of AUG methionine codons. Interestingly, the prp2-1 allele contains a point mutation that changes glycine to aspartate, indicating that EMT1-201 does not act by classical missense suppression. Extra copies of the tRNALeu(UAG) gene rescued the cold sensitivity and in vitro splicing defect of EMT1-201. This study provides the first example in which a mutation in a tRNA gene confers a pre-mRNA processing (prp) phenotype.

scholarly journals DEFICIENCY ANALYSIS OF THE TIP OF CHROMOSOME 3R IN DROSOPHILA MELANOGASTER

Genetics ◽  
1986 ◽  
Vol 112 (3) ◽  
pp. 539-550
Author(s):  
Kritaya Kongsuwan ◽  
Robert P Dellavalle ◽  
John R Merriam
Keyword(s):  
Drosophila Melanogaster ◽  
Genetic Analysis ◽  
X Chromosome ◽  
Genetic Manipulation ◽  
Chromosome Analysis ◽  
Chromosome 3 ◽  
Molecular Analyses ◽  
Number Of Genes ◽  
The Right ◽  
Minute Mutations

ABSTRACT Region 98EF-100F in chromosome 3 is interesting for genetic analysis because it contains a number of genes of developmental importance. Although there are no preexisting simple deficiency stocks, this region is amenable to genetic manipulation using other types of rearrangements. In the present investigation we obtained deficiencies by combining the terminal deficiencies formed by segregation of Y;3 translocations with a series of duplications of the tip of 3R, both from Y;3 translocations with different breakpoints and from 3;1 duplications in which the 3R tip is carried as a second arm on the X chromosome. Analysis of such synthetic deficiencies reveals five haplo-abnormal loci in the 98A-100F interval. These include a haplolethal site, a newly described Minute and three previously reported Minute mutations. The newly discovered Minute has been designated M(3)99D and is localized cytologically to bands 99D1-9. The three previously reported Minute loci in the region have been localized more precisely: M(3)1 to bands 99B5-9, M(3)f to bands 99E4-F1 and M(3)g to region 100C-F. In addition, we have been able to obtain synthetic deficiencies uncovering all of the intervals from 99B5 to 100B. These deficiencies will be useful for future genetic and molecular analyses of the genes that map within the right tip of chromosome 3.

scholarly journals TEMPERATURE-SENSITIVE MUTATIONS IN DROSOPHILA MELANOGASTER. IX. DOMINANT COLD-SENSITIVE LETHALS ON THE AUTOSOMES

Genetics ◽  
1972 ◽  
Vol 70 (1) ◽  
pp. 75-86
Author(s):  
Raja Rosenbluth ◽  
Dean Ezell ◽  
David T Suzuki
Keyword(s):  
Drosophila Melanogaster ◽  
Maternal Effect ◽  
Ethyl Methanesulfonate ◽  
Temperature Sensitive ◽  
Chromosome 2 ◽  
Prolonged Incubation ◽  
Larval Instars ◽  
Lethal Mutations ◽  
Cold Sensitive

ABSTRACT Ethyl methanesulfonate-treated autosomes were screened for the presence of dominant cold-sensitive (DCS) lethal mutations in Drosophila melanogaster. None was found among 6,552 treated and 168 untreated third chromosomes. Twenty-three DCS-L chromosomes which caused death at 17°C but survived at 22°C and 29°C were recovered from 5,046 mutagenized chromosome 2's.—The DCS-L mutations all mapped around dp and appeared to be functionally allelic. Lethality of heterozygotes for most of the DCS-L's occurred over a prolonged interval from the embryonic through the larval instars. Prolonged incubation at 17°C did not demonstrate any maternal effect on zygotic survival.

COLD-SENSITIVE CELL-DIVISION-CYCLE MUTANTS OF YEAST: ISOLATION, PROPERTIES, AND PSEUDOREVERSION STUDIES

Genetics ◽  
1982 ◽  
Vol 100 (4) ◽  
pp. 547-563 ◽  
Author(s):  
Don Moir ◽  
Sue E Stewart ◽  
Barbara C Osmond ◽  
David Botstein
Keyword(s):  
Cell Division ◽  
High Temperature ◽  
Nuclear Division ◽  
Cell Division Cycle ◽  
Cold Sensitivity ◽  
Temperature Sensitive ◽  
Sensitive Cell ◽  
Simultaneous Acquisition ◽  
Cold Sensitive ◽  
Cdc Genes

ABSTRACT We isolated 18 independent recessive cold-sensitive cell-division-cycle (cdc) mutants of Saccharomyces cerevisiae, in nine complementation groups. Terminal phenotypes exhibited include medial nuclear division, cytokinesis, and a previously undescribed terminal phenotype consisting of cells with a single small bud and an undivided nucleus. Four of the cold-sensitive mutants proved to be alleles of CDC11, while the remaining mutants defined at least six new cell-division-cycle genes: CDC44, CDC45, CDC48, CDC49, CDC50 and CDC51.—Spontaneous revertants from cold-sensitivity of four of the medial nuclear division cs cdc mutants were screened for simultaneous acquisition of a temperature-sensitive phenotype. The temperature-sensitive revertants of four different cs cdc mutants carried single new mutations, called Sup/Ts to denote their dual phenotype: suppression of the cold-sensitivity and concomitant conditional lethality at 37°. Many of the Sup/Ts mutations exhibited a cell-division-cycle terminal phenotype at the high temperature, and they defined two new cdc genes (CDC46 and CDC47). Two cold-sensitive medial nuclear division cdc mutants representing two different cdc genes were suppressed by different Sup/Ts alleles of another gene which also bears a medial nuclear division function (CDC46). In addition, the cold-sensitive medial nuclear division cdc mutant csH80 was suppressed by a Sup/Ts mutation yielding an unbudded terminal phenotype with an undivided nucleus at the high temperature. This mutation was an allele of CDC32. These results suggest a pattern of interaction among cdc gene products and indicate that cdc gene proteins might act in the cell cycle as complex specific functional assemblies.

scholarly journals Identification of Novel Genes Required for Yeast Pre-mRNA Splicing by Means of Cold-Sensitive Mutations

Genetics ◽  
1996 ◽  
Vol 143 (1) ◽  
pp. 67-80 ◽  
Author(s):  
Suzanne M Noble ◽  
Christine Guthrie
Keyword(s):  
Rna Splicing ◽  
Rna Helicase ◽  
Cold Sensitivity ◽  
Temperature Sensitive ◽  
Genetic Screens ◽  
Antiviral Protein ◽  
Novel Genes ◽  
New Class ◽  
Cold Sensitive ◽  
Complementation Groups

Abstract Genetic approaches in Saccharomyces cerevisiae have identified 38 genes required for efficient RNA splicing. The majority have been found by screening (high) temperature-sensitive (ts) mutants for those defective in splicing, an approach limited by the presence of ts hotspots and by the fact that many essential genes rarely mutate to the ts phenotype. To identify novel genes, we screened a collection of 340 cold-sensitive (cs) mutants for those that exhibited diminished splicing of several pre-mRNAs. We isolated 12 mutants in nine complementation groups. Four of these affected known genes (PRP8, PRP16, PRP22, PRP28), three of which encode RNA helicase homologues. Five genes are novel (BRR1, BRR2, BRR3, BRR4, BRR5; Bad Response to Refrigeration); mutations in these genes inhibited splicing before the first chemical step of the reaction. Analysis of BRR2 revealed it to encode an essential member of a new class of RNA helicase-like proteins that includes the yeast antiviral protein Ski2. These data validate the use of cs mutants in genetic screens and raise the possibility that RNA helicase family members are particularly prone to mutation to cold sensitivity.

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