FOXO regulates cell fate specification of Drosophila ventral olfactory projection neurons.

Abstract:

:Diverse types of neurons must be specified in the developing brain to form the functional neural circuits that are necessary for the execution of daily tasks. Here, we describe the participation of Forkhead box class O (FOXO) in cell fate specification of a small subset of Drosophila ventral olfactory projection neurons (vPNs). Using the two-color labeling system, twin-spot MARCM, we determined the temporal birth order of each vPN type, and this characterization served as a foundation to investigate regulators of cell fate specification. Flies deficient for chinmo, a known temporal cell fate regulator, exhibited a partial loss of vPNs, suggesting that the gene plays a complex role in specifying vPN cell fate and is not the only regulator of this process. Interestingly, loss of foxo function resulted in the precocious appearance of late-born vPNs in place of early-born vPNs, whereas overexpression of constitutively active FOXO caused late-born vPNs to take on a morphology reminiscent of earlier born vPNs. Taken together, these data suggest that FOXO temporally regulates vPN cell fate specification. The comprehensive identification of molecules that regulate neuronal fate specification promises to provide a better understanding of the mechanisms governing the formation of functional brain tissue.

journal_name

J Neurogenet

journal_title

Journal of neurogenetics

authors

Wei JY,Chung PC,Chu SY,Yu HH

doi

10.1080/01677063.2018.1556651

subject

Has Abstract

pub_date

2019-03-01 00:00:00

pages

33-40

issue

1

eissn

0167-7063

issn

1563-5260

journal_volume

33

pub_type

杂志文章
  • A genetic variant in the morphology of the medial preoptic area in mice.

    abstract::Inbred mice of the DBA/2J and C57BL/6J strains are known to differ in physiological and behavioral characteristics that are partially controlled by nuclei in the preoptic area/anterior hypothalamus. We describe a distinguishing nucleus of darkly staining, densely packed cells, which we term the medioventral pars compa...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677068509101424

    authors: Robinson SM,Fox TO,Sidman RL

    更新日期:1985-12-01 00:00:00

  • The role of human-specific gene duplications during brain development and evolution.

    abstract::One of the most fascinating questions in evolutionary biology is how traits unique to humans, such as their high cognitive abilities, erect bipedalism, and hairless skin, are encoded in the genome. Recent advances in genomics have begun to reveal differences between the genomes of the great apes. It has become evident...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677063.2013.789512

    authors: Sassa T

    更新日期:2013-09-01 00:00:00

  • A rare form of limb girdle muscular dystrophy (type 2E) seen in an Iranian family detected by autozygosity mapping.

    abstract::Sarcoglycanopathies (SGPs) constitute a subgroup of autosomal recessive limb girdle muscular dystrophies (LGMDs) which are caused by mutations in sarcoglycan (SGs) genes. SG proteins form a core complex consisting of α, β, γ and δ sarcoglycans which are encoded by SGCA, SGCB, SGCG and SGCD genes, respectively. Genetic...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677063.2016.1141208

    authors: Mojbafan M,Nilipour Y,Tonekaboni SH,Bagheri SD,Bagherian H,Sharifi Z,Zeinali Z,Tavakkoly-Bazzaz J,Zeinali S

    更新日期:2016-03-01 00:00:00

  • A touching story.

    abstract::A slide taped to a window at the Woods Hole Marine Biology Laboratory was my first introduction to the touch receptor neurons of the nematode Caenorhabditis elegans. Studying these cells as a postdoc with Sydney Brenner gave me a chance to work with John Sulston on a fascinating set of neurons. I would never have gues...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.1080/01677063.2020.1833879

    authors: Chalfie M

    更新日期:2020-09-01 00:00:00

  • A qualitative and quantitative light microscopic study of the inferior olivary complex in the adult staggerer mutant mouse.

    abstract::In the homozygous staggerer (sg/sg) mutant mouse, most of the Purkinje cells (the primary targets for olivocerebellar climbing fibers) are missing or ectopic. In this study, the organization and cell number of the inferior olivary complex in sg/sg were determined and compared to the inferior olive of the wildtype (+/+...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677068509100143

    authors: Blatt GJ,Eisenman LM

    更新日期:1985-02-01 00:00:00

  • Biallelic ZNF335 mutations cause basal ganglia abnormality with progressive cerebral/cerebellar atrophy.

    abstract::To date, less than 10 pedigrees have been reported with ZNF335 mutations since it was discovered in 2012 and little is known about ZNF335-related clinical spectrum. We describe a 12 years old male patient who is only child of nonconsanguineous Turkish parents. Trio whole genome sequencing identified previously unrepor...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.1080/01677063.2020.1833006

    authors: Caglayan AO,Yaghouti K,Kockaya T,Kemer D,Cankaya T,Ameziane N,Cogulu O,Coker M,Yalcinkaya C

    更新日期:2020-11-20 00:00:00

  • C. elegans: a sensible model for sensory biology.

    abstract::From Sydney Brenner's backyard to hundreds of labs across the globe, inspiring six Nobel Prize winners along the way, Caenorhabditis elegans research has come far in the past half century. The journey is not over. The virtues of C. elegans research are numerous and have been recounted extensively. Here, we focus on th...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.1080/01677063.2020.1823386

    authors: Iliff AJ,Xu XZS

    更新日期:2020-09-01 00:00:00

  • Kinase-mediated signaling cascades in mood disorders and antidepressant treatment.

    abstract::Kinase-mediated signaling cascades regulate a number of different molecular mechanisms involved in cellular homeostasis, and are viewed as one of the most common intracellular processes that are robustly dysregulated in the pathophysiology of mood disorders such as depression. Newly emerged, rapid acting antidepressan...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章,评审

    doi:10.1080/01677063.2016.1245303

    authors: Yuan LL,Wauson E,Duric V

    更新日期:2016-01-01 00:00:00

  • Neural control of homosexual courtship in Drosophila melanogaster.

    abstract::Immature D. melanogaster males, like virgin females, often elicit vigorous courtship from mature males. Since males perform the same behaviors in response to attractive males and females, the question arises as to whether the foci--cells in the courting male's nervous system that must be haplo-X for the fly to perform...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677068909107103

    authors: Napolitano LM,Tompkins L

    更新日期:1989-11-01 00:00:00

  • A histone modification identifies a DNA element controlling slo BK channel gene expression in muscle.

    abstract::The slo gene encodes the BK-type Ca(2+)-activated K(+) channels. In Drosophila, expression of slo is induced by organic solvent sedation (benzyl alcohol and ethanol), and this increase in neural slo expression contributes to the production of functional behavioral tolerance (inducible resistance) to these drugs. Withi...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677063.2015.1050097

    authors: Li X,Ghezzi A,Krishnan HR,Pohl JB,Bohm AY,Atkinson NS

    更新日期:2015-01-01 00:00:00

  • Gene polymorphisms associated with temperament.

    abstract::When individuals are exposed to stressful environmental challenges, the response varies widely in one or more of three components: psychology, behavior and physiology. This variability among individuals can be defined as temperament. In recent years, an increasing large body of evidence suggests that the dimensions of...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章,评审

    doi:10.1080/01677063.2017.1324857

    authors: Qiu X,Martin GB,Blache D

    更新日期:2017-01-01 00:00:00

  • Structural brain mutants: mushroom body defect (mud): a case study.

    abstract::Single-gene mutants of Drosophila have not only increased our understanding of the biochemical processes underlying learning and memory processes, but also established structure-function relationships. The first relevant mutants were identified by Martin Heisenberg nearly 30 years ago in a screen for altered adult bra...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章,评审

    doi:10.1080/01677060802471700

    authors: Hovhanyan A,Raabe T

    更新日期:2009-01-01 00:00:00

  • The serotonin transporter expression in Drosophila melanogaster.

    abstract::The serotonin transporter is an important regulator of serotonergic signaling. In order to analyze where the Drosophila melanogaster ortholog of the mammalian serotonin transporter (dSERT) is expressed in the nervous system, a dSERT antibody serum was used. Ectopic expression studies and loss of function analysis reve...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677063.2011.553002

    authors: Giang T,Ritze Y,Rauchfuss S,Ogueta M,Scholz H

    更新日期:2011-03-01 00:00:00

  • The murine mutation trembler-J: proof of semidominant expression by use of the linked vestigial tail marker.

    abstract::Trembler-J, TrJ, is a peripheral hypomyelinating murine mutant. In intercrosses (TrJ/ + X TrJ/ +) there are severely affected (behaviorally and pathologically), mildly affected, and normal offspring, while backcrosses (TrJ/ + X + / +) produce only mildly affected and normal offspring. We used the closely linked marker...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677068309107071

    authors: Henry EW,Sidman RL

    更新日期:1983-09-01 00:00:00

  • The Drosophila larval neuromuscular junction as a model for scaffold complexes at glutamatergic synapses: benefits and limitations.

    abstract::Based on unbeatable genetic accessibility and relative simplicity, the Drosophila larval neuromuscular junction has become a widely used model system for studying functional and structural aspects of excitatory glutamatergic synapses. Membrane-associated guanylate kinase-like proteins (MAGUKs) are first-order scaffold...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章,评审

    doi:10.3109/01677063.2010.493589

    authors: Thomas U,Kobler O,Gundelfinger ED

    更新日期:2010-09-01 00:00:00

  • The evolution and development of neural superposition.

    abstract::Visual systems have a rich history as model systems for the discovery and understanding of basic principles underlying neuronal connectivity. The compound eyes of insects consist of up to thousands of small unit eyes that are connected by photoreceptor axons to set up a visual map in the brain. The photoreceptor axon ...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章,评审

    doi:10.3109/01677063.2014.922557

    authors: Agi E,Langen M,Altschuler SJ,Wu LF,Zimmermann T,Hiesinger PR

    更新日期:2014-09-01 00:00:00

  • RNA editing in the Drosophila DMCA1A calcium-channel alpha 1 subunit transcript.

    abstract::Messenger RNA editing of transcripts encoding voltage-sensitive ion channels has not been extensively analyzed--least of all in Drosophila, for which several channel-encoding genes are known. Previous sequence studies of D. melanogaster's cacophony gene, which encodes an alpha 1 calcium-channel subunit called Dmca1A, ...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677069809108560

    authors: Smith LA,Peixoto AA,Hall JC

    更新日期:1998-11-01 00:00:00

  • The early years of Drosophila chemosensory genetics in Mumbai's Tata Institute of Fundamental Research.

    abstract::Some of the very first chemosensory mutants in Drosophila were generated in screens done in the 1970s at Obaid Siddiqi's lab in Tata Institute of Fundamental Research (TIFR), Mumbai. This is a personal account of some of the early work with these mutants, which led to their physiological and molecular characterization...

    journal_title:Journal of neurogenetics

    pub_type: 历史文章,杂志文章

    doi:10.3109/01677063.2012.677880

    authors: Hasan G

    更新日期:2012-09-01 00:00:00

  • Behavioral phenotypic properties of a natural occurring rat model of congenital stationary night blindness with Cacna1f mutation.

    abstract::Cacna1f gene mutation could lead to incomplete congenital stationary night blindness (iCSNB) disease. The CSNB-like phenotype rat is a spontaneous rat model caused by Cacna1f gene mutation. The present study explored the phenotypic properties of behavior performance in CSNB rats further. The vision-related behaviors o...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677063.2012.684416

    authors: An J,Wang L,Guo Q,Li L,Xia F,Zhang Z

    更新日期:2012-09-01 00:00:00

  • The irre cell recognition module (IRM) protein Kirre is required to form the reciprocal synaptic network of L4 neurons in the Drosophila lamina.

    abstract::Each neuropil module, or cartridge, in the fly's lamina has a fixed complement of cells. Of five types of monopolar cell interneurons, only L4 has collaterals that invade neighboring cartridges. In the proximal lamina, these collaterals form reciprocal synapses with both the L2 of their own cartridge and the L4 collat...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677063.2014.883390

    authors: Lüthy K,Ahrens B,Rawal S,Lu Z,Tarnogorska D,Meinertzhagen IA,Fischbach KF

    更新日期:2014-09-01 00:00:00

  • Dopamine DRD2 polymorphism (DRD2/ANNK1-Taq1A) is not a significant risk factor in writer's cramp.

    abstract::Writers' cramp is a movement disorder with dystonic co-contraction of fingers and hand during writing and is part of the clinical spectrum of focal dystonias. Previous studies showed reduced striatal dopamine receptor D2 (DRD2) availability in dystonia. The expression of D2 receptors is modulated by a DRD2/ANKK1-Taq1A...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.1080/01677063.2016.1238916

    authors: Zeuner KE,Acewicz A,Knutzen A,Dressler D,Lohmann K,Witt K

    更新日期:2016-01-01 00:00:00

  • Prevalence of the fragile X syndrome in Yugoslav patients with non-specific mental retardation.

    abstract::Mutations at two fragile sites, FRAXA and FRAXE, loci are caused by an expansion of a CGG/GCC trinucleotide repeat and are characterized by mental retardation. Here we report molecular screening survey of 97 unrelated individuals diagnosed with non-specific mental retardation (MR), which produced positive test for FRA...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.1080/neg.17.2-3.223.230

    authors: Major T,Culjkovic B,Stojkovic O,Gucscekic M,Lakic A,Romac S

    更新日期:2003-04-01 00:00:00

  • Optomotor-blind in the development of the Drosophila HS and VS lobula plate tangential cells.

    abstract::The horizontal system and vertical system cells of the dipteran optic lobes are well understood regarding their physiology and role in visually guided behavior. Little is known, however, about their development. Drosophila optomotor-blind (omb) is required for the development of the HS/VS cells which are lacking in th...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677063.2014.917645

    authors: Sen A,Grimm S,Hofmeyer K,Pflugfelder GO

    更新日期:2014-09-01 00:00:00

  • Noradrenergic gating of long-lasting synaptic potentiation in the hippocampus: from neurobiology to translational biomedicine.

    abstract::Altered synaptic strength underlies information storage in neural circuits. Neuromodulatory transmitters such as norepinephrine (NE) facilitate long-lasting synaptic plasticity by recruiting and modifying multiple molecular elements of synaptic signaling, including specific transmitter receptors, intracellular protein...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章,评审

    doi:10.1080/01677063.2018.1497630

    authors: Nguyen PV,Gelinas JN

    更新日期:2018-09-01 00:00:00

  • Behavioral Plasticity in the C. elegans Mechanosensory Circuit.

    abstract::This review outlines research into the cellular and molecular mechanisms underlying a simple behavior in the soil-dwelling nematode, C. elegans. A tap administered to the side of a petri plate acts as a nonlocalized mechanical stimulus to the worms within. Most adult worms respond to this tap stimulus with backward lo...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章,评审

    doi:10.1080/01677060802298509

    authors: Ardiel EL,Rankin CH

    更新日期:2008-01-01 00:00:00

  • Dopamine modulates female sexual receptivity in Drosophila melanogaster.

    abstract::Newly eclosed Drosophila melanogaster flies were systemically depleted of dopamine by feeding an inhibitor of the biosynthetic enzyme, tyrosine hydroxylase, and analyzed for abnormalities in courtship behavior. Dopamine-depleted females were significantly less receptive to males than were control females, although mal...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677069809167259

    authors: Neckameyer WS

    更新日期:1998-03-01 00:00:00

  • Behavior, genetics and biochemistry of an allele of the mutant mouse spastic, spaAlb.

    abstract::A new autosomal recessive mutation, characterized by an early defect in righting reflex and stiffened gait, progression to severe spasticity, tremor and rigidity, and death before weaning, appeared spontaneously on the C57BL/6 background. It was shown to be an allele of the mutant spastic spa, and shall be known as sp...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:

    authors: White WF,Regan LJ,Roe AW,Messer A

    更新日期:1987-08-01 00:00:00

  • The regulations of Drosophila phototransduction.

    abstract::This is the first of two reviews that include some of the studies that we, members of the Pak lab and collaborators, carried out from 1998 to 2010 on the functional and physical interactions among several Drosophila phototransduction components. The report includes our studies on the regulations and/or the functions o...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章,评审

    doi:10.3109/01677063.2011.650253

    authors: Leung HT,Shino S,Kim E

    更新日期:2012-06-01 00:00:00

  • Phosphoinositide metabolism in Drosophila phototransduction: a coffee break discussion leads to 30 years of history.

    abstract::The aim of this review is to summarize the history of Dr. Yoshiki Hotta and his collaborators' contributions to the research field of Drosophila phototransduction. The electroretinogram-defective mutants reported in 1970 by Dr. Hotta and Dr. Seymour Benzer in the article entitled "Genetic dissection of the Drosophila ...

    journal_title:Journal of neurogenetics

    pub_type: 传,历史文章,杂志文章

    doi:10.3109/01677063.2011.647144

    authors: Suzuki E,Masai I,Inoue H

    更新日期:2012-03-01 00:00:00

  • Inter-tissue networks between the basal forebrain, hippocampus, and prefrontal cortex in a model for depression caused by disturbed sleep.

    abstract::Disturbances in sleep are encountered in the majority of patients with depressive disorder. To elucidate the molecular mechanisms behind this relationship, we examined gene expression changes in a rodent model for disturbed sleep and depression. The animals were treated with daily injections of clomipramine to affect ...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677063.2012.694932

    authors: Lagus M,Gass N,Saharinen J,Savelyev S,Porkka-Heiskanen T,Paunio T

    更新日期:2012-09-01 00:00:00