Drosophila rosA gene, which when mutant causes aberrant photoreceptor oscillation, encodes a novel neurotransmitter transporter homologue.

Abstract:

:The Drosophila receptor oscillation A (rosA) mutations, which cause electroretinogram (ERG) defects, including oscillations, were localized to the 24F4-25A2 region of chromosome 2L. Genomic fragments from this region, isolated from bacteriophage P1 clones, included those that detect transcriptional defects in rosA mutants in RNA blot experiments. One of these genomic fragments was used to screen a head cDNA library. The largest cDNA clone (3.6 kb) isolated was shown to rescue a rosA mutant in P element-germline transformation experiments. The ROSA protein deduced from the open reading frame in the 3.6 kb rosA cDNA is 943 amino acids long and is 36-41% identical to members of the superfamily of Na+/Cl(-)-dependent neurotransmitter transporters, with no indication of higher sequence identity to any one subgroup within the superfamily. RNA blot experiments revealed multiple transcripts in various developmental stages, the most abundant one being a 3.7 kb transcript, particularly in the adult head. Tissue in situ experiments identified the rosA transcript to be localized to many tissues, with higher levels of hybridization in the nervous system and digestive tract. The results demonstrate that the rosA gene encodes a novel Na+/Cl(-)-dependent transporter important for normal response properties of the photoreceptor.

journal_name

J Neurogenet

journal_title

Journal of neurogenetics

authors

Burg MG,Geng C,Guan Y,Koliantz G,Pak WL

doi

10.3109/01677069609107063

subject

Has Abstract

pub_date

1996-12-01 00:00:00

pages

59-79

issue

1-2

eissn

0167-7063

issn

1563-5260

journal_volume

11

pub_type

杂志文章
  • 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

  • Some mutations affecting neural or muscular tissues alter the physiological components of the electroretinogram in Drosophila.

    abstract::Mutants displaying generalized behavioral defects and one mutant having an enzyme deficiency were examined for electroretinogram (ERG) defects. Mutations in nine genes were examined that cause ERG defects. Two, parats4 and slrpD, cause reversibly temperature dependent loss of the off-transients in the ERG. stnC and Ty...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677068909167263

    authors: Homyk T Jr,Pye Q

    更新日期:1989-01-01 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

  • Helmsman is expressed in both trachea and photoreceptor development: partial inactivation alters tracheal morphology and visually guided behavior.

    abstract::We have identified helmsman (hlm), which is expressed in the fruit fly photoreceptor cells during neural network development. Hlm is also expressed in the elongating cells of the embryonic trachea. Both photoreceptor neurons and embryonic trachea cells elongate in precise, targeted growth for cell-to-cell specific rec...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.1080/01677060801893276

    authors: McKay JP,Nightingale B,Pollock JA

    更新日期:2008-01-01 00:00:00

  • Aging-associated alteration of telomere length and subtelomeric status in female patients with Parkinson's disease.

    abstract::A telomere is a repetitive DNA structure at chromosomal ends that stabilizes the chromosome structure and prevents harmful end-to-end recombinations. The telomere length of somatic cells becomes shorter with aging because of the "end replication problem." This telomere shortening is accelerated by pathophysiological c...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677063.2011.651665

    authors: Maeda T,Guan JZ,Koyanagi M,Higuchi Y,Makino N

    更新日期:2012-06-01 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

  • Individual differences in sensory responses influence decision making by Drosophila melanogaster larvae on exposure to contradictory cues.

    abstract::Animals make decisions on behavioral choice by evaluating internal and external signals. Individuals often make decisions in different ways, but the underlying neural mechanisms are not well understood. Here, we describe a system for observing the behavior of individual Drosophila melanogaster larvae simultaneously pr...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.1080/01677063.2016.1202949

    authors: Koseki N,Mori S,Suzuki S,Tonooka Y,Kosugi S,Miyakawa H,Morimoto T

    更新日期:2016-01-01 00:00:00

  • Trap a gene and find out its function: toward functional genomics in Drosophila.

    abstract::Many declared aims of the genome projects have been achieved. The total genomic sequences of several relatively noncomplex/complex organisms (such as E. coli, yeast, Caenorhabditis, Drosophila) are being determined, and the nucleotide sequencing of the entire human genome will be complete in the near future. However, ...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章,评审

    doi:10.3109/01677060109167373

    authors: Lukacsovich T,Yamamoto D

    更新日期:2001-01-01 00:00:00

  • Strain-selective effects of nicotine on electrophysiological responses evoked in hippocampus from DBA/2Ibg and C3H/2Ibg mice.

    abstract::We used the hippocampal slice to examine extracellular electrophysiological responses to nicotine and the difference in sensitivity to nicotine-induced electrophysiological effects between the DBA and C3H mouse strains. Nicotine enhanced CA1 population spikes (PS) evoked by Schaffer collateral stimulation in a concent...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:

    authors: Freund RK,Wehner JM

    更新日期:1987-04-01 00:00:00

  • Identification of a Drosophila presenilin homologue: evidence of alternatively spliced forms.

    abstract::Some cases of Alzheimer's disease are inherited as a dominant trait in humans. To date, mutations in three genes account for some of them: the amyloid precursor protein (APP) and presenilins 1 and 2 (PS-1 and PS-2, respectively). The function of the presenilins is still unclear, although they belong to a transmembrane...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677069809108554

    authors: Marfany G,Del-Favero J,Valero R,De Jonghe C,Woodrow S,Hendriks L,Van Broeckhoven C,Gonzàlez-Duarte R

    更新日期:1998-01-01 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

  • A novel mutation in the gene encoding noggin is not causative in human neural tube defects.

    abstract::Neural tube defects (NTD) are a common birth defect, with both genetic and environmental contributions to their etiology. In mouse, null mutations in Noggin result in fully-penetrant NTDs. We investigated Noggin for mutations that may predispose to human NTDs in 202 NTD cases. One variant allele was identified in a ma...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:

    authors: Bauer KA,George TM,Enterline DS,Stottmann RW,Melvin EC,Siegel D,Samal S,Hauser MA,Klingensmith J,Nye JS,Speer MC,Neural Tube Defects Collaborative Group.

    更新日期:2002-01-01 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

  • Variation in the vitamin D receptor gene is associated with multiple sclerosis in an Australian population.

    abstract::Multiple Sclerosis (MS) is a chronic inflammatory demyelinating disease of the central nervous system (CNS) resulting in accumulating neurological disability. The disorder is more prevalent at higher latitudes. To investigate VDR gene variation using three intragenic restriction fragment length polymorphisms (Apa I, T...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.1080/01677060590949692

    authors: Tajouri L,Ovcaric M,Curtain R,Johnson MP,Griffiths LR,Csurhes P,Pender MP,Lea RA

    更新日期:2005-01-01 00:00:00

  • 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

  • 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

  • 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 neuro...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.1080/01677063.2018.1556651

    authors: Wei JY,Chung PC,Chu SY,Yu HH

    更新日期:2019-03-01 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

  • 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

  • Cell lineage relationships in the development of the mammalian CNS. II. Bilateral independence of CNS clones.

    abstract::This report contains additional observations on the cell lineage relationships of the motor neurons of the facial nucleus and of the cerebellar Purkinje cells of the mouse. These cell populations were quantitatively analyzed in the mosaic brains of experimental aggregation chimeras. The cell markers used to perform th...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677068409107092

    authors: Herrup K,Wetts R,Diglio TJ

    更新日期:1984-12-01 00:00:00

  • Role of hippocampal Met-enkephalin in the genotype-dependent regulation of exploratory behavior in mice.

    abstract::Intrahippocampal microinjections with anti-Met-enkephalin antiserum enhanced novelty-induced vertically oriented exploratory acts and horizontal locomotor activity in inbred mouse strain DBA/2 and reduced these behaviors in C57BL/6 so that strain differences originally present between the normal serum controls were el...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677068609106848

    authors: van Abeelen JH,Gerads HJ

    更新日期:1986-05-01 00:00:00

  • Distinct mechanisms of action of the Lozenge locus in Drosophila eye and antennal development are suggested by the analysis of dominant enhancers.

    abstract::The development of the olfactory sense organs on the antenna of the fruit fly Drosophila utilises mechanisms distinct from those used in the rest of the adult peripheral nervous system. Lozenge (lz) is the only locus hither-to identified as required for the development of antennal sense organs. In addition to effects ...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677069509083460

    authors: Gupta BP,Rodrigues V

    更新日期:1995-12-01 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

  • 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

  • Isogenic autosomes to be applied in optimal screening for novel mutants with viable phenotypes in Drosophila melanogaster.

    abstract::Most insertional mutagenesis screens of Drosophila performed to date have not used target chromosomes that have been checked for their suitability for phenotypic screens for viable phenotypes. To address this, we have generated a selection of stocks carrying either isogenized second chromosomes or isogenized third chr...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.1080/01677060591007155

    authors: Sharma P,Asztalos Z,Ayyub C,de Bruyne M,Dornan AJ,Gomez-Hernandez A,Keane J,Killeen J,Kramer S,Madhavan M,Roe H,Sherkhane PD,Siddiqi K,Silva E,Carlson JR,Goodwin SF,Heisenberg M,Krishnan K,Kyriacou CP,Partridge L,

    更新日期:2005-04-01 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 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

  • Notch signaling is required for activity-dependent synaptic plasticity at the Drosophila neuromuscular junction.

    abstract::The cell-surface-signaling protein Notch, is required for numerous developmental processes and typically specifies which of two adjacent cells will adopt a non-neuronal developmental fate. It has recently been implicated in long-term memory formation in mammals and Drosophila. Here, we investigated whether activity-de...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677060902878481

    authors: de Bivort BL,Guo HF,Zhong Y

    更新日期:2009-01-01 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

  • High frequency of mutations in the PIK3CA gene helical and kinase coding regions in a group of Iranian patients with high-grade glioblastomas: five novel mutations.

    abstract::Glioblastoma multiform (GBM; World Health Organization (WHO) grade IV) and anaplastic astrocytomas (AA; WHO grade III) are highly aggressive and lethal astrocytic brain tumors. To detect cancer-specific somatic mutations in two hot-spot regions of PIK3CA gene, the helical and kinase domains (encoded by exons 9 and 20,...

    journal_title:Journal of neurogenetics

    pub_type: 杂志文章

    doi:10.3109/01677063.2011.623202

    authors: Derakhshandeh-Peykar P,Alivi J,Hossein-nezhad A,Rautenstrauss B,Vesal RE,Doriani A

    更新日期:2011-12-01 00:00:00