A conserved long noncoding RNA affects sleep behavior in Drosophila.

Abstract:

:Metazoan genomes encode an abundant collection of mRNA-like, long noncoding (lnc)RNAs. Although lncRNAs greatly expand the transcriptional repertoire, we have a limited understanding of how these RNAs contribute to developmental regulation. Here, we investigate the function of the Drosophila lncRNA called yellow-achaete intergenic RNA (yar). Comparative sequence analyses show that the yar gene is conserved in Drosophila species representing 40-60 million years of evolution, with one of the conserved sequence motifs encompassing the yar promoter. Further, the timing of yar expression in Drosophila virilis parallels that in D. melanogaster, suggesting that transcriptional regulation of yar is conserved. The function of yar was defined by generating null alleles. Flies lacking yar RNAs are viable and show no overt morphological defects, consistent with maintained transcriptional regulation of the adjacent yellow (y) and achaete (ac) genes. The location of yar within a neural gene cluster led to the investigation of effects of yar in behavioral assays. These studies demonstrated that loss of yar alters sleep regulation in the context of a normal circadian rhythm. Nighttime sleep was reduced and fragmented, with yar mutants displaying diminished sleep rebound following sleep deprivation. Importantly, these defects were rescued by a yar transgene. These data provide the first example of a lncRNA gene involved in Drosophila sleep regulation. We find that yar is a cytoplasmic lncRNA, suggesting that yar may regulate sleep by affecting stabilization or translational regulation of mRNAs. Such functions of lncRNAs may extend to vertebrates, as lncRNAs are abundant in neural tissues.

journal_name

Genetics

journal_title

Genetics

authors

Soshnev AA,Ishimoto H,McAllister BF,Li X,Wehling MD,Kitamoto T,Geyer PK

doi

10.1534/genetics.111.131706

subject

Has Abstract

pub_date

2011-10-01 00:00:00

pages

455-68

issue

2

eissn

0016-6731

issn

1943-2631

pii

genetics.111.131706

journal_volume

189

pub_type

杂志文章

相关文献

GENETICS文献大全
  • Estimation of linkage in the presence of multiplicative viability effects.

    abstract::Log-linear analysis of contingency tables is applied to trihybrid backcross data to estimate linkage and viability. Whereas nonadditive viability differences perturb recombination estimates in the classical analysis, this statistical procedure yields maximum likelihood crossover frequency estimates in the presence of ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Clark AG

    更新日期:1981-09-01 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 multiple roles of gld-1 in germline development: interactions with the sex determination cascade and the glp-1 signaling pathway.

    abstract::The Caenorhabditis elegans gene gld-1 is essential for oocyte development; in gld-1 (null) hermaphrodites, a tumor forms where oogenesis would normally occur. We use genetic epistasis analysis to demonstrate that tumor formation is dependent on the sexual fate of the germline. When the germline sex determination pathw...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Francis R,Maine E,Schedl T

    更新日期:1995-02-01 00:00:00

  • Mapping quantitative trait loci for expression abundance.

    abstract::Mendelian loci that control the expression levels of transcripts are called expression quantitative trait loci (eQTL). When mapping eQTL, we often deal with thousands of expression traits simultaneously, which complicates the statistical model and data analysis. Two simple approaches may be taken in eQTL analysis: (1)...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.106.065599

    authors: Jia Z,Xu S

    更新日期:2007-05-01 00:00:00

  • Mutational analysis of the open reading frames in the transposable element IS1.

    abstract::IS1 is one of the smallest transposable elements found in bacteria (768 bp). It contains eight overlapping open-reading-frames (ORFs) greater than 50 codons, designated insA to insG and insB'. To determine which of the ORFs actually code for proteins involved in transposition, we have introduced amber codons into each...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Jakowec M,Prentki P,Chandler M,Galas DJ

    更新日期:1988-09-01 00:00:00

  • Genetic analysis of size-scaling patterns in the mouse mandible.

    abstract::The relationship between multidimensional form of the adult mouse mandible and body size is examined from an ontogenetic perspective. The origin and ontogeny of phenotypic correlations are described in terms of genetic and environmental covariance patterns between adult skeletal morphology and growth in body weight. D...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Atchley WR,Plummer AA,Riska B

    更新日期:1985-11-01 00:00:00

  • Assembly of the mitochondrial membrane system: nuclear suppression of a cytochrome b mutation in yeast mitochondrial DNA.

    abstract::In a previous study, a mitochondrial mutant expressing a specific enzymatic deficiency in co-enzyme QH2-cytochrome c reductase was described (TZAGO-LOFF, FOURY and AKAI 1976). Analysis of the mitochondrially translated proteins revealed the absence in the mutant of the mitochondrial product corresponding to cytochrome...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Coruzzi G,Tzagoloff A

    更新日期:1980-08-01 00:00:00

  • The Genetics of Mating Song Evolution Underlying Rapid Speciation: Linking Quantitative Variation to Candidate Genes for Behavioral Isolation.

    abstract::Differences in mating behaviors evolve early during speciation, eventually contributing to reproductive barriers between species. Knowledge of the genetic and genomic basis of these behaviors is therefore integral to a causal understanding of speciation. Acoustic behaviors are often part of the mating ritual in animal...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.118.301706

    authors: Xu M,Shaw KL

    更新日期:2019-03-01 00:00:00

  • Clinal variation for amino acid polymorphisms at the Pgm locus in Drosophila melanogaster.

    abstract::Clinal variation is common for enzymes in the glycolytic pathway for Drosophila melanogaster and is generally accepted as an adaptive response to different climates. Although the enzyme phosphoglucomutase (PGM) possesses several allozyme polymorphisms, it is unique in that it had been reported to show no clinal variat...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Verrelli BC,Eanes WF

    更新日期:2001-04-01 00:00:00

  • Cell polarity in Saccharomyces cerevisiae depends on proper localization of the Bud9 landmark protein by the EKC/KEOPS complex.

    abstract::In diploid Saccharomyces cerevisiae cells, bud-site selection is determined by two cortical landmarks, Bud8p and Bud9p, at the distal and proximal poles, respectively. Their localizations depend on the multigenerational proteins Rax1p/Rax2p. Many genes involved in bud-site selection were identified previously by genom...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.111.128231

    authors: Kato Y,Kawasaki H,Ohyama Y,Morishita T,Iwasaki H,Kokubo T,Hirano H

    更新日期:2011-08-01 00:00:00

  • Roles for WHITE COLLAR-1 in circadian and general photoperception in Neurospora crassa.

    abstract::The transcription factors WHITE COLLAR-1 (WC-1) and WHITE COLLAR-2 (WC-2) interact to form a heterodimeric complex (WCC) that is essential for most of the light-mediated processes in Neurospora crassa. WCC also plays a distinct non-light-related role as the transcriptional activator in the FREQUENCY (FRQ)/WCC feedback...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Lee K,Dunlap JC,Loros JJ

    更新日期:2003-01-01 00:00:00

  • Analysis of conditional genetic effects and variance components in developmental genetics.

    abstract::A genetic model with additive-dominance effects and genotype x environment interactions is presented for quantitative traits with time-dependent measures. The genetic model for phenotypic means at time t conditional on phenotypic means measured at previous time (t-1) is defined. Statistical methods are proposed for an...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Zhu J

    更新日期:1995-12-01 00:00:00

  • The neutral coalescent process for recent gene duplications and copy-number variants.

    abstract::I describe a method for simulating samples from gene families of size two under a neutral coalescent process, for the case where the duplicate gene either has fixed recently in the population or is still segregating. When a duplicate locus has recently fixed by genetic drift, diversity in the new gene is expected to b...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.107.074948

    authors: Thornton KR

    更新日期:2007-10-01 00:00:00

  • Developmental genetics of the 2E-F region of the Drosophila X chromosome: a region rich in "developmentally important" genes.

    abstract::We have analyzed the 2E1-3A1 area of the X chromosome with special attention to loci related to embryogenesis. Published maps indicate that this chromosomal segment contains ten bands. Our genetic analysis has identified 11 complementation groups: one recessive visible (prune), two female steriles and eight lethals. O...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Perrimon N,Engstrom L,Mahowald AP

    更新日期:1984-11-01 00:00:00

  • Repeated Selection of Alternatively Adapted Haplotypes Creates Sweeping Genomic Remodeling in Stickleback.

    abstract::Heterogeneous genetic divergence can accumulate across the genome when populations adapt to different habitats while still exchanging alleles. How long does diversification take and how much of the genome is affected? When divergence occurs in parallel from standing genetic variation, how often are the same haplotypes...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.117.300610

    authors: Bassham S,Catchen J,Lescak E,von Hippel FA,Cresko WA

    更新日期:2018-07-01 00:00:00

  • A genetic locus having trans and contiguous cis functions that control the disproportionate replication of ribosomal RNA genes in Drosophila melanogaster.

    abstract::The results of deficiency mapping experiments reveal the presence of a compensatory response (cr+) locus that is located distal to the cluster of ribosomal RNA (rRNA) genes and is responsible for disproportionately replicating these genes when cr+ locus is present in a single dose, as in X/O males or X/sc4-sc8 females...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Procunier JD,Tartof KD

    更新日期:1978-01-01 00:00:00

  • MNR2 regulates intracellular magnesium storage in Saccharomyces cerevisiae.

    abstract::Magnesium (Mg) is an essential enzyme cofactor and a key structural component of biological molecules, but relatively little is known about the molecular components required for Mg homeostasis in eukaryotic cells. The yeast genome encodes four characterized members of the CorA Mg transporter superfamily located in the...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.109.106419

    authors: Pisat NP,Pandey A,Macdiarmid CW

    更新日期:2009-11-01 00:00:00

  • Distributive disjunction of authentic chromosomes in Saccharomyces cerevisiae.

    abstract::Distributive disjunction is defined as the first division meiotic segregation of either nonhomologous chromosomes that lack homologs or homologous chromosomes that have not recombined. To determine if chromosomes from the yeast Saccharomyces cerevisiae were capable of distributive disjunction, we constructed a strain ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Guacci V,Kaback DB

    更新日期:1991-03-01 00:00:00

  • unc-44 Ankyrin and stn-2 gamma-syntrophin regulate sax-7 L1CAM function in maintaining neuronal positioning in Caenorhabditis elegans.

    abstract::The L1 family of single-pass transmembrane cell adhesion molecules (L1CAMs) is conserved from Caenorhabditis elegans and Drosophila to vertebrates and is required for axon guidance, neurite outgrowth, and maintenance of neuronal positions. The extracellular region of L1CAMs mediates cell adhesion via interactions with...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.108.091272

    authors: Zhou S,Opperman K,Wang X,Chen L

    更新日期:2008-11-01 00:00:00

  • 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

  • Screens for piwi suppressors in Drosophila identify dosage-dependent regulators of germline stem cell division.

    abstract::The Drosophila piwi gene is the founding member of the only known family of genes whose function in stem cell maintenance is highly conserved in both animal and plant kingdoms. piwi mutants fail to maintain germline stem cells in both male and female gonads. The identification of piwi-interacting genes is essential fo...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Smulders-Srinivasan TK,Lin H

    更新日期:2003-12-01 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

  • Crossover interference on nucleolus organizing region-bearing chromosomes in Arabidopsis.

    abstract::In most eukaryotes, crossovers are not independently distributed along the length of a chromosome. Instead, they appear to avoid close proximity to one another--a phenomenon known as crossover interference. Previously, for three of the five Arabidopsis chromosomes, we measured the strength of interference and suggeste...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.104.040055

    authors: Lam SY,Horn SR,Radford SJ,Housworth EA,Stahl FW,Copenhaver GP

    更新日期:2005-06-01 00:00:00

  • The contribution of the Y chromosome to hybrid male sterility in house mice.

    abstract::Hybrid sterility in the heterogametic sex is a common feature of speciation in animals. In house mice, the contribution of the Mus musculus musculus X chromosome to hybrid male sterility is large. It is not known, however, whether F1 male sterility is caused by X-Y or X-autosome incompatibilities or a combination of b...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.112.141804

    authors: Campbell P,Good JM,Dean MD,Tucker PK,Nachman MW

    更新日期:2012-08-01 00:00:00

  • Frequency-dependent selection and the maintenance of genetic variation: exploring the parameter space of the multiallelic pairwise interaction model.

    abstract::When individuals' fitnesses depend on the genetic composition of the population in which they are found, selection is then frequency dependent. Frequency-dependent selection (FDS) is often invoked as a heuristic explanation for the maintenance of large numbers of alleles at a locus. The pairwise interaction model is a...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.107.073072

    authors: Trotter MV,Spencer HG

    更新日期:2007-07-01 00:00:00

  • Detecting local adaptation using the joint sampling of polymorphism data in the parental and derived populations.

    abstract::When a local colonization in a new niche occurs, the new derived population should be subject to different selective pressures from that in the original parental population; consequently it is likely that many loci will be subject to directional selection. In such a quick adaptation event through environmental changes...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.108.086835

    authors: Innan H,Kim Y

    更新日期:2008-07-01 00:00:00

  • Using allele frequencies and geographic subdivision to reconstruct gene trees within a species: molecular variance parsimony.

    abstract::We formalize the use of allele frequency and geographic information for the construction of gene trees at the intraspecific level and extend the concept of evolutionary parsimony to molecular variance parsimony. The central principle is to consider a particular gene tree as a variable to be optimized in the estimation...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Excoffier L,Smouse PE

    更新日期:1994-01-01 00:00:00

  • Molecular nature of spontaneous mutations in mouse lactate dehydrogenase-A processed pseudogenes.

    abstract::The presence of at least ten mouse LDH-A pseudogenes was demonstrated in the genomic blot analysis, and four different processed pseudogenes have thus far been isolated and characterized. In this report, the nucleotide sequences to two different mouse lactate dehydrogenase-A processed pseudogenes, M11 and M14, were de...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Fukasawa KM,Tanimura M,Sakai I,Sharief FS,Chung FZ,Li SS

    更新日期:1987-01-01 00:00:00

  • Deep haplotype divergence and long-range linkage disequilibrium at xp21.1 provide evidence that humans descend from a structured ancestral population.

    abstract::Fossil evidence links human ancestry with populations that evolved from modern gracile morphology in Africa 130,000-160,000 years ago. Yet fossils alone do not provide clear answers to the question of whether the ancestors of all modern Homo sapiens comprised a single African population or an amalgamation of distinct ...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:10.1534/genetics.105.041095

    authors: Garrigan D,Mobasher Z,Kingan SB,Wilder JA,Hammer MF

    更新日期:2005-08-01 00:00:00

  • Estimation of the amount of DNA polymorphism when the neutral mutation rate varies among sites.

    abstract::Knowing the amount of DNA polymorphism is essential to understand the mechanism of maintaining DNA polymorphism in a natural population. The amount of DNA polymorphism can be measured by the average number of nucleotide differences per site (pi), the proportion of segregating (polymorphic) site (s) and the minimum num...

    journal_title:Genetics

    pub_type: 杂志文章

    doi:

    authors: Misawa K,Tajima F

    更新日期:1997-12-01 00:00:00