Wingless Signaling: A Genetic Journey from Morphogenesis to Metastasis.

Abstract:

:This FlyBook chapter summarizes the history and the current state of our understanding of the Wingless signaling pathway. Wingless, the fly homolog of the mammalian Wnt oncoproteins, plays a central role in pattern generation during development. Much of what we know about the pathway was learned from genetic and molecular experiments in Drosophila melanogaster, and the core pathway works the same way in vertebrates. Like most growth factor pathways, extracellular Wingless/Wnt binds to a cell surface complex to transduce signal across the plasma membrane, triggering a series of intracellular events that lead to transcriptional changes in the nucleus. Unlike most growth factor pathways, the intracellular events regulate the protein stability of a key effector molecule, in this case Armadillo/β-catenin. A number of mysteries remain about how the "destruction complex" destabilizes β-catenin and how this process is inactivated by the ligand-bound receptor complex, so this review of the field can only serve as a snapshot of the work in progress.

journal_name

Genetics

journal_title

Genetics

authors

Bejsovec A

doi

10.1534/genetics.117.300157

subject

Has Abstract

pub_date

2018-04-01 00:00:00

pages

1311-1336

issue

4

eissn

0016-6731

issn

1943-2631

pii

genetics.117.300157

journal_volume

208

pub_type

杂志文章,评审

相关文献

GENETICS文献大全
  • Linkage disequilibrium in growing and stable populations.

    abstract::Nonrandom associations between alleles at different loci can be tested for using Fisher's exact test. Extensive simulations show that there is a substantial probability of obtaining significant nonrandom associations between closely or completely linked polymorphic neutral loci in a population of constant size at equi...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Slatkin M

    更新日期:1994-05-01 00:00:00

  • A novel mutation in DNA topoisomerase I of yeast causes DNA damage and RAD9-dependent cell cycle arrest.

    abstract::DNA topoisomerases, enzymes that alter the superhelicity of DNA, have been implicated in such critical cellular functions as transcription, DNA replication, and recombination. In the yeast Saccharomyces cerevisiae, a null mutation in the gene encoding topoisomerase I (TOP1) causes elevated levels of mitotic recombinat...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Levin NA,Bjornsti MA,Fink GR

    更新日期:1993-04-01 00:00:00

  • The unusual spectrum of mutations induced by hybrid dysgenesis at the Triplo-lethal locus of Drosophila melanogaster.

    abstract::The Triplo-lethal locus (Tpl) is unique in its dosage sensitivity; no other locus in Drosophila has been identified that is lethal when present in three doses. Tpl is also haplo-lethal, and its function is still a mystery. Previous workers have found it nearly impossible to mutationally inactive Tpl other than by comp...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Dorer DR,Christensen AC

    更新日期:1990-08-01 00:00:00

  • Maintaining two mating types: structure of the mating type locus and its role in heterokaryosis in Podospora anserina.

    abstract::Pseudo-homothallism is a reproductive strategy elected by some fungi producing heterokaryotic sexual spores containing genetically different but sexually compatible nuclei. This lifestyle appears as a compromise between true homothallism (self-fertility with predominant inbreeding) and complete heterothallism (with ex...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.113.159988

    authors: Grognet P,Bidard F,Kuchly C,Tong LC,Coppin E,Benkhali JA,Couloux A,Wincker P,Debuchy R,Silar P

    更新日期:2014-05-01 00:00:00

  • An interspecific backcross of Lycopersicon esculentum x L. hirsutum: linkage analysis and a QTL study of sexual compatibility factors and floral traits.

    abstract::A BC1 population of the self-compatible tomato Lycopersicon esculentum and its wild self-incompatible relative L. hirsutum f. typicum was used for restriction fragment length polymorphism linkage analysis and quantitative trait loci (QTL) mapping of reproductive behavior and floral traits. The self-incompatibility loc...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Bernacchi D,Tanksley SD

    更新日期:1997-10-01 00:00:00

  • Heterozygote Advantage Is a Common Outcome of Adaptation in Saccharomyces cerevisiae.

    abstract::Adaptation in diploids is predicted to proceed via mutations that are at least partially dominant in fitness. Recently, we argued that many adaptive mutations might also be commonly overdominant in fitness. Natural (directional) selection acting on overdominant mutations should drive them into the population but then,...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.115.185165

    authors: Sellis D,Kvitek DJ,Dunn B,Sherlock G,Petrov DA

    更新日期:2016-07-01 00:00:00

  • An Allosteric Network for Spliceosome Activation Revealed by High-Throughput Suppressor Analysis in Saccharomyces cerevisiae.

    abstract::Selection of suppressor mutations that correct growth defects caused by substitutions in an RNA or protein can reveal functionally important molecular structures and interactions in living cells. This approach is particularly useful for the study of complex biological pathways involving many macromolecules, such as pr...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.119.301922

    authors: Brow DA

    更新日期:2019-05-01 00:00:00

  • A comparison of mutation rates for specific loci and chromosome regions in dysgenic hybrid males of Drosophila melanogaster.

    abstract::The mutation rates of specific loci and chromosome regions were estimated for two types of dysgenic hybrid males. These came from crosses between P or Q males and M females in the P-M system of hybrid dysgenesis. The M X P hybrids were the more mutable for each of the loci and chromosome regions tested. The Beadex loc...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Simmons MJ,Raymond JD,Johnson NA,Fahey TM

    更新日期:1984-01-01 00:00:00

  • Detecting Rare Mutations with Heterogeneous Effects Using a Family-Based Genetic Random Field Method.

    abstract::The genetic etiology of many complex diseases is highly heterogeneous. A complex disease can be caused by multiple mutations within the same gene or mutations in multiple genes at various genomic loci. Although these disease-susceptibility mutations can be collectively common in the population, they are often individu...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.118.301266

    authors: Li M,He Z,Tong X,Witte JS,Lu Q

    更新日期:2018-10-01 00:00:00

  • Analysis of the inheritance, selection and evolution of growth trajectories.

    abstract::We present methods for estimating the parameters of inheritance and selection that appear in a quantitative genetic model for the evolution growth trajectories and other "infinite-dimensional" traits that we recently introduced. Two methods for estimating the additive genetic covariance function are developed, a "full...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Kirkpatrick M,Lofsvold D,Bulmer M

    更新日期:1990-04-01 00:00:00

  • Stable Patterns of CENH3 Occupancy Through Maize Lineages Containing Genetically Similar Centromeres.

    abstract::While the approximate chromosomal position of centromeres has been identified in many species, little is known about the dynamics and diversity of centromere positions within species. Multiple lines of evidence indicate that DNA sequence has little or no impact in specifying centromeres in maize and in most multicellu...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.115.177360

    authors: Gent JI,Wang K,Jiang J,Dawe RK

    更新日期:2015-08-01 00:00:00

  • Role of the Tsc1-Tsc2 complex in signaling and transport across the cell membrane in the fission yeast Schizosaccharomyces pombe.

    abstract::Heterozygous inactivation of either human TSC1 or TSC2 causes tuberous sclerosis (TSC), in which development of benign tumors, hamartomas, occurs via a two-hit mechanism. In this study, fission yeast genes homologous to TSC1 and TSC2 were identified, and their protein products were shown to physically interact like th...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Matsumoto S,Bandyopadhyay A,Kwiatkowski DJ,Maitra U,Matsumoto T

    更新日期:2002-07-01 00:00:00

  • A comprehensive study of genic variation in natural populations of Drosophila melanogaster. IV. Mitochondrial DNA variation and the role of history vs. selection in the genetic structure of geographic populations.

    abstract::Preliminary studies with restriction fragment length polymorphisms of mitochondrial DNA (mtDNA) in natural populations of Drosophila melanogaster revealed considerable variation in terms of nucleotide sequence and overall size. In this report we present data from more isofemale lines and more restriction enzymes, and ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Hale LR,Singh RS

    更新日期:1991-09-01 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

  • Characterization of an unusually conserved AluI highly reiterated DNA sequence family from the honeybee, Apis mellifera.

    abstract::An AluI family of highly reiterated nontranscribed sequences has been found in the genome of the honeybee Apis mellifera. This repeated sequence is shown to be present at approximately 23,000 copies per haploid genome constituting about 2% of the total genomic DNA. The nucleotide sequence of 10 monomers was determined...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Tarès S,Cornuet JM,Abad P

    更新日期:1993-08-01 00:00:00

  • Genetics on the Fly: A Primer on the Drosophila Model System.

    abstract::Fruit flies of the genus Drosophila have been an attractive and effective genetic model organism since Thomas Hunt Morgan and colleagues made seminal discoveries with them a century ago. Work with Drosophila has enabled dramatic advances in cell and developmental biology, neurobiology and behavior, molecular biology, ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.115.183392

    authors: Hales KG,Korey CA,Larracuente AM,Roberts DM

    更新日期:2015-11-01 00:00:00

  • Genomic Structure of Hstx2 Modifier of Prdm9-Dependent Hybrid Male Sterility in Mice.

    abstract::F1 hybrids between mouse inbred strains PWD and C57BL/6 represent the most thoroughly genetically defined model of hybrid sterility in vertebrates. Hybrid male sterility can be fully reconstituted from three components of this model, the Prdm9 gene, intersubspecific homeology of Mus musculus musculus and Mus musculus ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.119.302554

    authors: Lustyk D,Kinský S,Ullrich KK,Yancoskie M,Kašíková L,Gergelits V,Sedlacek R,Chan YF,Odenthal-Hesse L,Forejt J,Jansa P

    更新日期:2019-11-01 00:00:00

  • Functional studies of the carboxy-terminal repeat domain of Drosophila RNA polymerase II in vivo.

    abstract::To understand the in vivo function of the unique and conserved carboxy-terminal repeat domain (CTD) of RNA polymerase II largest subunit (RpII215), we have studied RNA polymerase II biosynthesis, activity and genetic function in Drosophila RpII215 mutants that possessed all (C4), half (W81) or none (IIt) of the CTD re...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Brickey WJ,Greenleaf AL

    更新日期:1995-06-01 00:00:00

  • Lack of spontaneous sister chromatid exchanges in somatic cells of Drosophila melanogaster.

    abstract::Neural ganglia of wild type third-instar larvae of Drosophila melanogaster were incubated for 13 hours at various concentrations of BUdR (1, 3, 9, 27 micrograms/ml). Metaphases were collected with colchicine, stained with Hoechst 33258, and scored under a fluorescence microscope. Metaphases in which the sister chromat...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Gatti M,Santini G,Pimpinelli S,Olivieri G

    更新日期:1979-02-01 00:00:00

  • Regulation of ribosome biogenesis by nucleostemin 3 promotes local and systemic growth in Drosophila.

    abstract::Nucleostemin 3 (NS3) is an evolutionarily conserved protein with profound roles in cell growth and viability. Here we analyze cell-autonomous and non-cell-autonomous growth control roles of NS3 in Drosophila and demonstrate its GTPase activity using genetic and biochemical assays. Two null alleles of ns3, and RNAi, de...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.112.149104

    authors: Hartl TA,Ni J,Cao J,Suyama KL,Patchett S,Bussiere C,Gui DY,Tang S,Kaplan DD,Fish M,Johnson AW,Scott MP

    更新日期:2013-05-01 00:00:00

  • The EGL-4 PKG acts with KIN-29 salt-inducible kinase and protein kinase A to regulate chemoreceptor gene expression and sensory behaviors in Caenorhabditis elegans.

    abstract::The regulation of chemoreceptor (CR) gene expression by environmental signals and internal cues may contribute to the modulation of multiple physiological processes and behavior in Caenorhabditis elegans. We previously showed that KIN-29, a homolog of salt-inducible kinase, acts in sensory neurons to regulate the expr...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.108.094771

    authors: van der Linden AM,Wiener S,You YJ,Kim K,Avery L,Sengupta P

    更新日期:2008-11-01 00:00:00

  • Exegeses on maximum genetic differentiation.

    abstract::A canon of population genetics concerns the properties of FST, a descriptor of spatial genetic structure. Interest for FST arose from Wright's early insights linking FST to dispersal parameters as well as to his concept of effective population size (e.g., Wright 1938, 1951). Although there is continued interest in thi...

    journal_title:Genetics

    pub_type: 评论,杂志文章

    doi:10.1534/genetics.113.152132

    authors: Rousset F

    更新日期:2013-07-01 00:00:00

  • A selfish gene governing pollen-pistil compatibility confers reproductive isolation between maize relatives.

    abstract::Some populations of maize's closest relatives, the annual teosintes of Mexico, are unreceptive to maize pollen. When present in the pistil (silk and ovary) a number of maize genes discriminate against or exclude pollen not carrying the same allele. An analogous gene Tcb1-s was found in some teosinte populations but no...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.105.048645

    authors: Kermicle JL

    更新日期:2006-01-01 00:00:00

  • Quantitative trait locus study design from an information perspective.

    abstract::We examine the efficiency of different genotyping and phenotyping strategies in inbred line crosses from an information perspective. This provides a mathematical framework for the statistical aspects of QTL experimental design, while guiding our intuition. Our central result is a simple formula that quantifies the fra...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.104.038612

    authors: Sen S,Satagopan JM,Churchill GA

    更新日期:2005-05-01 00:00:00

  • Synaptonemal Complex Central Region Proteins Promote Localization of Pro-crossover Factors to Recombination Events During Caenorhabditis elegans Meiosis.

    abstract::Crossovers (COs) between homologous chromosomes are critical for meiotic chromosome segregation and form in the context of the synaptonemal complex (SC), a meiosis-specific structure that assembles between aligned homologs. During Caenorhabditis elegans meiosis, central region components of the SC (SYP proteins) are e...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.119.302625

    authors: Cahoon CK,Helm JM,Libuda DE

    更新日期:2019-10-01 00:00:00

  • Bayesian quantitative trait locus mapping using inferred haplotypes.

    abstract::We describe a fast hierarchical Bayesian method for mapping quantitative trait loci by haplotype-based association, applicable when haplotypes are not observed directly but are inferred from multiple marker genotypes. The method avoids the use of a Monte Carlo Markov chain by employing priors for which the likelihood ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.109.113183

    authors: Durrant C,Mott R

    更新日期:2010-03-01 00:00:00

  • A Gene Regulatory Program in Human Breast Cancer.

    abstract::Molecular heterogeneity in human breast cancer has challenged diagnosis, prognosis, and clinical treatment. It is well known that molecular subtypes of breast tumors are associated with significant differences in prognosis and survival. Assuming that the differences are attributed to subtype-specific pathways, we then...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.115.180125

    authors: Li R,Campos J,Iida J

    更新日期:2015-12-01 00:00:00

  • High-resolution sex-specific linkage maps of the mouse reveal polarized distribution of crossovers in male germline.

    abstract::Since the publication of the first comprehensive linkage map for the laboratory mouse, the architecture of recombination as a basic biological process has become amenable to investigation in mammalian model organisms. Here we take advantage of high-density genotyping and the unique pedigree structure of the incipient ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.114.161653

    authors: Liu EY,Morgan AP,Chesler EJ,Wang W,Churchill GA,Pardo-Manuel de Villena F

    更新日期:2014-05-01 00:00:00

  • Modeling the zebrafish segmentation clock's gene regulatory network constrained by expression data suggests evolutionary transitions between oscillating and nonoscillating transcription.

    abstract::During segmentation of vertebrate embryos, somites form in accordance with a periodic pattern established by the segmentation clock. In the zebrafish (Danio rerio), the segmentation clock includes six hairy/enhancer of split-related (her/hes) genes, five of which oscillate due to negative autofeedback. The nonoscillat...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.114.163642

    authors: Schwendinger-Schreck J,Kang Y,Holley SA

    更新日期:2014-06-01 00:00:00

  • The isolation and characterization of Saccharomyces cerevisiae mutants that constitutively express purine biosynthetic genes.

    abstract::In response to an external source of adenine, yeast cells repress the expression of purine biosynthesis pathway genes. To identify necessary components of this signalling mechanism, we have isolated mutants that are constitutively active for expression. These mutants were named bra (for bypass of repression by adenine...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Guetsova ML,Lecoq K,Daignan-Fornier B

    更新日期:1997-10-01 00:00:00