Patterns of gene variation in central and marginal populations of Drosophila robusta.

Abstract:

:The central and marginal populations of D. robusta differ greatly in the level of inversion polymorphism; the marginal populations are monomorphic or nearly so and the central populations are highly polymorphic. This paper presents the frequencies of alleles at forty gene loci in various populations of D. robusta, studied by electrophoresis of proteins and enzymes. Population samples were obtained from eight widely separated populations of D. robusta which included the central, the extreme marginal and the intervening populations between the center and the margins. We find that the proportion of polymorphic loci and average heterozygosity per individual is slightly higher in the marginal populations than the central populations. In D. robusta on an average, 39% of the loci are polymorphic and the average proportion of loci heterozygous per individual is 11%. A breakdown of loci in three categories, viz, hydrolytic enzymes and some other enzymes, larval proteins and glycolytic and Kreb's cycle enzymes, shows that in all populations the level of polymorphism is highest in the hydrolytic enzymes, intermediate in larval proteins and least in the glycolytic and Kreb's cycle enzymes. On the average, the proportion of loci heterozygous per individual for three groups of loci is: hydrolytic enzymes and others (.164), larval proteins (.115) and glycolytic and Kreb's cycle enzymes (.037). We also observe that in all populations the level of polymorphism on the X chromosome is far less than the expected 38%; in salivary gland cells the euchromatic length of the X chromosome is 38% of the entire genome. Lower levels of polymorphism for the X chromosome loci are explained due to low probability of balanced polymorphisms for the X-linked loci since the conditions for establishment of balanced polymorphism for X-linked loci are more restrictive than for the autosomal loci.-The polymorphic loci can be grouped according to pattern of allele frequencies in different populations as follows: (1) The allele frequencies are similar in all populations at the XDH, Pep-1 and Hex-1 loci. (2) The alleles at the Est-1, Est-2, Amy loci and the AP-4(1.0) and the LAP-1(.90) alleles show north south clinal change in frequency. (3) There is north south and east west differentiation at the Pt-5, Pt-8 and Pt-9 loci and the allele AP-4(.81). (4) Polymorphism at loci such as Fum, B.Ox, Hex-8, Pep-2 and Pep-3 are restricted to only one or two of the populations. (5) Allele frequencies at the MDH and ODH loci fluctuate between populations. (6) Allele frequencies at many polymorphic loci such as Est-1, Est-2, LAP-1, AP-4, Pt-5, Pt-8, Pt-9, Pt-16, MDH, Fum change clinally within a gene arrangement. The pattern of gene variation in D. robusta is very complex and cannot be easily explained due to migration of neutral alleles between once-isolated populations or to semi-isolation of neutral alleles. The observations of the pattern of allele variation in different populations, high levels of polymorphism in the marginal populations which have small population size and low levels of polymorphism of the X chromosome loci all support the argument in favor of balancing selection as the main mechanism for the maintenance of these polymorphisms. Environmental factors must play a role in the maintenance of a great deal of these polymorphisms, since we observe clinal allele frequency changes even within a given inversion type.

journal_name

Genetics

journal_title

Genetics

authors

Prakash S

subject

Has Abstract

pub_date

1973-10-01 00:00:00

pages

347-69

issue

2

eissn

0016-6731

issn

1943-2631

journal_volume

75

pub_type

杂志文章

相关文献

GENETICS文献大全
  • The population genetics of synthetic lethals.

    abstract::Synthetic lethals are variants at different loci that have little or no effect on viability singly but cause lethality in combination. The importance of synthetic lethals and, more generally, of synthetic deleterious loci (SDL) has been controversial. Here, we derive the expected frequencies for SDL under a mutation-s...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Phillips PC,Johnson NA

    更新日期:1998-09-01 00:00:00

  • Temporal Action of Mutations Inhibiting the Accomplishment of Quiescence or Disrupting Development in the Fungus PODOSPORA ANSERINA.

    abstract::Two Podospora mutants carrying mutations modE and modF were persumed to be quiescent defective, because, when grown under glucose limitation, they differed from the wild-type strain in an excess of dry weight production and a reduction of cell survival. New insight on the action of modE and modF mutations was provided...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Durrens P,Bernet J

    更新日期:1985-01-01 00:00:00

  • Genetic Control of Recombination in SCHIZOPHYLLUM COMMUNE: Location of a Gene Controlling B-Factor Recombination.

    abstract::In S. commune the frequency of recombination between the two subunits, alpha and beta, of the B incompatibility factor is genetically controlled. Analysis of the progeny obtained from crosses between high- and low-recombining strains indicates that the gene controlling recombination frequency in the B factor is linked...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Koltin Y,Stamberg J

    更新日期:1973-05-01 00:00:00

  • Identification of residues in fission yeast and human p34cdc2 required for S-M checkpoint control.

    abstract::In fission yeast, regulation of p34cdc2 plays an important role in the checkpoint coupling mitosis to completion of DNA replication. The cdc2 mutations cdc2-3w (C67Y) and cdc2-4w (C67F) abolish checkpoint control without seriously affecting normal cell proliferation. However the molecular basis of this phenotype is no...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Basi G,Enoch T

    更新日期:1996-12-01 00:00:00

  • Rmr6 maintains meiotic inheritance of paramutant states in Zea mays.

    abstract::Paramutation generates heritable changes affecting regulation of specific alleles found at several Zea mays (maize) loci that encode transcriptional regulators of anthocyanin biosynthetic genes. Although the direction and extent of paramutation is influenced by poorly understood allelic interactions occurring in diplo...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.105.045260

    authors: Hollick JB,Kermicle JL,Parkinson SE

    更新日期:2005-10-01 00:00:00

  • Major effects on teratogen-induced facial clefting in mice determined by a single genetic region.

    abstract::A major correlation has been found between the incidence of glucocorticoid-induced cleft palate and the chromosome 8 segment identified by N-acetyl transferase in mice. The resistant strain became fully susceptible while the susceptible strain became resistant when this chromosomal region, representing less than 0.7% ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Karolyi J,Erickson RP,Liu S,Killewald L

    更新日期:1990-09-01 00:00:00

  • A genetic model for control of hypertriglyceridemia and apolipoprotein B levels in the Johns Hopkins colony of St. Thomas Hospital rabbits.

    abstract::The St. Thomas Hospital (STH) rabbit has been previously shown to have a Mendelian form of hypertriglyceridemia, accompanied by accelerated atherosclerosis, and these animals may serve as a useful model for human dyslipoproteinemia syndromes. Here we describe the establishment of a new colony of these STH animals, and...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Beaty TH,Prenger VL,Virgil DG,Lewis B,Kwiterovich PO,Bachorik PS

    更新日期:1992-12-01 00:00:00

  • Quantitative Measurement of the Ability of Different Mutagens to Induce an Inherited Change in Phenotype to Allow Maltose Utilization in Suspension Cultures of the Soybean, GLYCINE MAX (L.) Merr.

    abstract::USING A NEWLY DEVELOPED PLATING SYSTEM, WE HAVE MEASURED CELL SURVIVAL AND THE FREQUENCIES OF VARIATION IN AN INHERITED TRAIT AFTER TREATMENT OF SOYBEAN CELL SUSPENSIONS WITH DIFFERENT MUTAGENS: ethyl methanesulfonate (EMS), methyl methanesulfonate (MMS), N-Methyl-N'-nitro-N-nitroso-guanidine (MNNG), hycanthone (1-{[2...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Weber G,Lark KG

    更新日期:1980-09-01 00:00:00

  • Fitness effects of EMS-induced mutations on the X chromosome of Drosophila melanogaster. I. Viability effects and heterozygous fitness effects.

    abstract::Drosophila melanogaster X chromosomes were mutagenized by feeding males sucrose solutions containing ethyl methanesulfonate (EMS); the concentrations of EMS in the food were 2.5 mM, 5.0 mM, and 10.0 mM. Chromosomes were exposed to the mutagen up to three times by treating males in succeeding generations. After treatme...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Mitchell JA

    更新日期:1977-12-01 00:00:00

  • Fixation probability in a two-locus model by the ancestral recombination-selection graph.

    abstract::We use the ancestral influence graph (AIG) for a two-locus, two-allele selection model in the limit of a large population size to obtain an analytic approximation for the probability of ultimate fixation of a single mutant allele A. We assume that this new mutant is introduced at a given locus into a finite population...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.111.136309

    authors: Lessard S,Kermany AR

    更新日期:2012-02-01 00:00:00

  • The mutator gene swi8 effects specific mutations in the mating-type region of Schizosaccharomyces pombe.

    abstract::The swi8+ gene of Schizosaccharomyces pombe appears to be involved in the termination step of copy synthesis during mating-type (MT) switching. Mutations in swi8 confer a general mutator phenotype and, in particular, generate specific mutations in the MT region. Sequencing of the MT cassettes of the h90 swi8-137 mutan...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Fleck O,Rudolph C,Albrecht A,Lorentz A,Schär P,Schmidt H

    更新日期:1994-11-01 00:00:00

  • A genetic screen for increased loss of heterozygosity in Saccharomyces cerevisiae.

    abstract::Loss of heterozygosity (LOH) can be a driving force in the evolution of mitotic/somatic diploid cells, and cellular changes that increase the rate of LOH have been proposed to facilitate this process. In the yeast Saccharomyces cerevisiae, spontaneous LOH occurs by a number of mechanisms including chromosome loss and ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.108.089250

    authors: Andersen MP,Nelson ZW,Hetrick ED,Gottschling DE

    更新日期:2008-07-01 00:00:00

  • The role of breeding and genetics in animal production improvement in the developing countries.

    abstract::Availability of animal protein for human consumption is very low in the developing countries mainly because of low productivity of existing livestock; ways and means to improve productivity through breeding are discussed and some basic issues requiring further research pointed out. ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Rendel J

    更新日期:1974-09-01 00:00:00

  • Spatial autocorrelation of genotypes under directional selection.

    abstract::The spatial distributions of genetic variation under selection-mutation equilibrium within populations that have limited dispersal are investigated. The results show that directional selection with moderate strength rapidly reduces the amount of genetic structure and spatial autocorrelations far below that predicted f...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Epperson BK

    更新日期:1990-03-01 00:00:00

  • Inducing segmental aneuploid mosaicism in the mouse through targeted asymmetric sister chromatid event of recombination.

    abstract::Loss or gain of whole chromosomes, or parts of chromosomes, is found in various pathological conditions, such as cancer and aneuploidy, and results from the missegregation of chromosomes during cellular division or abnormal mitotic recombination. We introduce a novel strategy for determining the consequences of segmen...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.108.092312

    authors: Duchon A,Besson V,Pereira PL,Magnol L,Hérault Y

    更新日期:2008-09-01 00:00:00

  • Studies of Linkage in Populations. IX. the Effect of Altitude on X-Chromosomal Arrangement Combinations in DROSOPHILA ROBUSTA.

    abstract::Data are presented concerning the gene arrangements in both arms of the X-chromosome of Drosophila robusta in eight altitudinal transects. The major change appears to be the increase of gene arrangement XL-1 (and decrease in XL, sometimes also XL-2) with increasing altitude. In each transect only one combination of XL...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Levitan M

    更新日期:1978-08-01 00:00:00

  • The role of a pollen-expressed Cullin1 protein in gametophytic self-incompatibility in Solanum.

    abstract::We previously isolated a pollen factor, ui6.1, which encodes a Cullin1 protein (CUL1) that functions in unilateral interspecific incompatibility (UI) in Solanum. Here we show that CUL1 is also required for pollen function in self-incompatibility (SI). We used RNA interference (RNAi) to reduce CUL1 expression in pollen...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.113.158279

    authors: Li W,Chetelat RT

    更新日期:2014-02-01 00:00:00

  • A cladistic measure of gene flow inferred from the phylogenies of alleles.

    abstract::A method for estimating the average level of gene flow among populations is introduced. The method provides an estimate of Nm, where N is the size of each local population in an island model and m is the migration rate. This method depends on knowing the phylogeny of the nonrecombining segments of DNA that are sampled...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Slatkin M,Maddison WP

    更新日期:1989-11-01 00:00:00

  • The Effect of Inbreeding on Competitive Male-Mating Ability in DROSOPHILA MELANOGASTER.

    abstract::The effect of full-sib inbreeding on competitive male-mating ability (CImale symbol) in Drosophila melanogaster was investigated in two experiments. In the first, five inbred lines (with reserves) were assessed up to 18 generations. Linear inbreeding depression, of 5.9% per 10% increase in homozygosity, was observed. ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Sharp PM

    更新日期:1984-04-01 00:00:00

  • Null mutations in the lin-31 gene indicate two functions during Caenorhabditis elegans vulval development.

    abstract::The lin-31 gene is required for the proper specification of vulval cell fates in the nematode Caenorhabditis elegans and encodes a member of the winged-helix family of transcription factors. Members of this important family have been identified in many organisms and are known to bind specific DNA targets involved in a...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Miller LM,Hess HA,Doroquez DB,Andrews NM

    更新日期:2000-12-01 00:00:00

  • Measuring selection coefficients affecting the alcohol dehydrogenase polymorphism in Drosophila melanogaster.

    abstract::This paper describes a perturbation experiment on the frequency of the F and S Alcohol dehydrogenase (Adh) alleles of D. melanogaster. Fifty-four iso-female lines set up from three wild populations and with initial F frequencies of either 0.25, 0.50 or 0.75 were maintained on standard laboratory food medium at 22 degr...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Wilson SR,Oakeshott JG,Gibson JB,Anderson PR

    更新日期:1982-01-01 00:00:00

  • Partial exclusion between T-even bacteriophages: an incipient genetic isolation mechanism.

    abstract::Conditional lethal mutant systems developed in T-even bacteriophages T2, T4 and T6 have been used to study the partial exclusion which characterizes mixed infections of these phages. In bacteria mixedly infected with T2 and T4, the dominant phage (T4) acts against localized exclusion sensitivity determinants in the ge...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Russell RL,Huskey RJ

    更新日期:1974-12-01 00:00:00

  • Unique and Overlapping Functions of Formins Frl and DAAM During Ommatidial Rotation and Neuronal Development in Drosophila.

    abstract::The noncanonical Frizzled/planar cell polarity (PCP) pathway regulates establishment of polarity within the plane of an epithelium to generate diversity of cell fates, asymmetric, but highly aligned structures, or to orchestrate the directional migration of cells during convergent extension during vertebrate gastrulat...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.115.181438

    authors: Dollar G,Gombos R,Barnett AA,Sanchez Hernandez D,Maung SM,Mihály J,Jenny A

    更新日期:2016-03-01 00:00:00

  • A key transcription cofactor on the nascent sex chromosomes of European tree frogs (Hyla arborea).

    abstract::We show that MED15, a key component of the transcription complex Mediator, lies within the nonrecombining segment of nascent sex chromosomes in the male-heterogametic Hyla arborea. Both X and Y alleles are expressed during embryonic development and differ by three frame-preserving indels (eight amino acids in total) w...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.108.090746

    authors: Niculita-Hirzel H,Stöck M,Perrin N

    更新日期:2008-07-01 00:00:00

  • Centromere locations and associated chromosome rearrangements in Arabidopsis lyrata and A. thaliana.

    abstract::We analyzed linkage and chromosomal positions of genes in A. lyrata ssp. petraea that are located near the centromere (CEN) regions of A. thaliana, using at least two genes from the short and long arms of each chromosome. In our map, genes from all 10 A. thaliana chromosome arms are also tightly linked in A. lyrata. G...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.106.057182

    authors: Kawabe A,Hansson B,Hagenblad J,Forrest A,Charlesworth D

    更新日期:2006-07-01 00:00:00

  • EOR-2 is an obligate binding partner of the BTB-zinc finger protein EOR-1 in Caenorhabditis elegans.

    abstract::BTB-zinc finger transcription factors play many important roles in metazoan development. In these proteins, the BTB domain is critical for dimerization and for recruiting cofactors to target genes. Identification of these cofactors is important for understanding how BTB-zinc finger proteins influence transcription. He...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.109.111591

    authors: Howell K,Arur S,Schedl T,Sundaram MV

    更新日期:2010-04-01 00:00:00

  • Rhythmic Behavior Is Controlled by the SRm160 Splicing Factor in Drosophila melanogaster.

    abstract::Circadian clocks organize the metabolism, physiology, and behavior of organisms throughout the day-night cycle by controlling daily rhythms in gene expression at the transcriptional and post-transcriptional levels. While many transcription factors underlying circadian oscillations are known, the splicing factors that ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.117.300139

    authors: Beckwith EJ,Hernando CE,Polcowñuk S,Bertolin AP,Mancini E,Ceriani MF,Yanovsky MJ

    更新日期:2017-10-01 00:00:00

  • Domains of heterochromatin protein 1 required for Drosophila melanogaster heterochromatin spreading.

    abstract::Centric regions of eukaryotic genomes are packaged into heterochromatin, which possesses the ability to spread along the chromosome and silence gene expression. The process of spreading has been challenging to study at the molecular level due to repetitious sequences within centric regions. A heterochromatin protein 1...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.109.105338

    authors: Hines KA,Cryderman DE,Flannery KM,Yang H,Vitalini MW,Hazelrigg T,Mizzen CA,Wallrath LL

    更新日期:2009-08-01 00:00:00

  • The centenary of Janssens's chiasmatype theory.

    abstract::The segregation and random assortment of characters observed by Mendel have their basis in the behavior of chromosomes in meiosis. But showing this actually to be the case requires a correct understanding of the meiotic behavior of chromosomes. This was achieved only gradually, over several decades, with much dispute ...

    journal_title:Genetics

    pub_type: 传,历史文章,杂志文章

    doi:10.1534/genetics.112.139733

    authors: Koszul R,Meselson M,Van Doninck K,Vandenhaute J,Zickler D

    更新日期:2012-06-01 00:00:00

  • Quantitative trait loci mapping and the genetic basis of heterosis in maize and rice.

    abstract::Despite its importance to agriculture, the genetic basis of heterosis is still not well understood. The main competing hypotheses include dominance, overdominance, and epistasis. NC design III is an experimental design that has been used for estimating the average degree of dominance of quantitative trait loci (QTL) a...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.107.082867

    authors: Garcia AA,Wang S,Melchinger AE,Zeng ZB

    更新日期:2008-11-01 00:00:00