Localized surface activity of torso, a receptor tyrosine kinase, specifies terminal body pattern in Drosophila.

Abstract:

:The subdivision of the Drosophila body into distinct terminal and central domains depends on the torso (tor) protein, a putative receptor tyrosine kinase that is active at both ends of the early embryo. We show that the tor protein is uniformly expressed along the surface membrane of early embryos despite its localized activity at both poles. Further, we present evidence that polarized activity of this protein depends on other terminal gene functions, one of which may be a localized extracellular ligand generated during oogenesis. Finally, using the temperature-sensitive gain-of-function mutation torRL3, we show that different levels of active tor protein can specify distinct portions of the terminal pattern. Thus, we argue (1) that for functions as a ubiquitous surface receptor that is activated by a spatially restricted ligand, and (2) that localized activity of the tor kinase may generate one or more gradients of intracellular signals that control body pattern.

journal_name

Genes Dev

journal_title

Genes & development

authors

Casanova J,Struhl G

doi

10.1101/gad.3.12b.2025

subject

Has Abstract

pub_date

1989-12-01 00:00:00

pages

2025-38

issue

12B

eissn

0890-9369

issn

1549-5477

journal_volume

3

pub_type

杂志文章
  • Pcf11 orchestrates transcription termination pathways in yeast.

    abstract::In Saccharomyces cerevisiae, short noncoding RNA (ncRNA) generated by RNA polymerase II (Pol II) are terminated by the NRD complex consisting of Nrd1, Nab3, and Sen1. We now show that Pcf11, a component of the cleavage and polyadenylation complex (CPAC), is also generally required for NRD-dependent transcription termi...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.251470.114

    authors: Grzechnik P,Gdula MR,Proudfoot NJ

    更新日期:2015-04-15 00:00:00

  • I kappa B interacts with the nuclear localization sequences of the subunits of NF-kappa B: a mechanism for cytoplasmic retention.

    abstract::NF-kappa B is an inducible transcription factor comprised of a 50-kD (p50) and a 65-kD (p65) subunit. Induction of NF-kappa B activity, which is a critical event in many signal transduction pathways, involves release from a cytoplasmic inhibitory protein, I kappa B, followed by translocation of the active transcriptio...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.6.10.1899

    authors: Beg AA,Ruben SM,Scheinman RI,Haskill S,Rosen CA,Baldwin AS Jr

    更新日期:1992-10-01 00:00:00

  • Cytosolic signaling protein Ecsit also localizes to mitochondria where it interacts with chaperone NDUFAF1 and functions in complex I assembly.

    abstract::Ecsit is a cytosolic adaptor protein essential for inflammatory response and embryonic development via the Toll-like and BMP (bone morphogenetic protein) signal transduction pathways, respectively. Here, we demonstrate a mitochondrial function for Ecsit (an evolutionary conserved signaling intermediate in Toll pathway...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.408407

    authors: Vogel RO,Janssen RJ,van den Brand MA,Dieteren CE,Verkaart S,Koopman WJ,Willems PH,Pluk W,van den Heuvel LP,Smeitink JA,Nijtmans LG

    更新日期:2007-03-01 00:00:00

  • Mad2 prevents aneuploidy and premature proteolysis of cyclin B and securin during meiosis I in mouse oocytes.

    abstract::In mitosis, the spindle checkpoint protein Mad2 averts aneuploidy by delaying anaphase onset until chromosomes align. Here we show that depletion of Mad2 in meiosis I mouse oocytes induced an increased incidence of aneuploidy. Proteolysis of cyclin B and securin commenced earlier in Mad2-depleted oocytes, resulting in...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.328105

    authors: Homer HA,McDougall A,Levasseur M,Yallop K,Murdoch AP,Herbert M

    更新日期:2005-01-15 00:00:00

  • Caudal, a key developmental regulator, is a DPE-specific transcriptional factor.

    abstract::The regulation of gene transcription is critical for the proper development and growth of an organism. The transcription of protein-coding genes initiates at the RNA polymerase II core promoter, which is a diverse module that can be controlled by many different elements such as the TATA box and downstream core promote...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.1698108

    authors: Juven-Gershon T,Hsu JY,Kadonaga JT

    更新日期:2008-10-15 00:00:00

  • Loss of TET2 in hematopoietic cells leads to DNA hypermethylation of active enhancers and induction of leukemogenesis.

    abstract::DNA methylation is tightly regulated throughout mammalian development, and altered DNA methylation patterns are a general hallmark of cancer. The methylcytosine dioxygenase TET2 is frequently mutated in hematological disorders, including acute myeloid leukemia (AML), and has been suggested to protect CG dinucleotide (...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.260174.115

    authors: Rasmussen KD,Jia G,Johansen JV,Pedersen MT,Rapin N,Bagger FO,Porse BT,Bernard OA,Christensen J,Helin K

    更新日期:2015-05-01 00:00:00

  • Cyclin D3 coordinates the cell cycle during differentiation to regulate erythrocyte size and number.

    abstract::Genome-wide association studies (GWASs) have identified a genetic variant of moderate effect size at 6p21.1 associated with erythrocyte traits in humans. We show that this variant affects an erythroid-specific enhancer of CCND3. A Ccnd3 knockout mouse phenocopies these erythroid phenotypes, with a dramatic increase in...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.197020.112

    authors: Sankaran VG,Ludwig LS,Sicinska E,Xu J,Bauer DE,Eng JC,Patterson HC,Metcalf RA,Natkunam Y,Orkin SH,Sicinski P,Lander ES,Lodish HF

    更新日期:2012-09-15 00:00:00

  • Loss of Daxx, a promiscuously interacting protein, results in extensive apoptosis in early mouse development.

    abstract::The mammalian Daxx gene has been identified in a diverse set of yeast interaction trap experiments. Although a facilitating role for Daxx in Fas-induced apoptosis has been suggested, Daxx's physiologic function remains unknown. To elucidate the in vivo role of Daxx, we have generated Daxx-deficient mice. Surprisingly,...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.13.15.1918

    authors: Michaelson JS,Bader D,Kuo F,Kozak C,Leder P

    更新日期:1999-08-01 00:00:00

  • Polar localization of the replication origin and terminus in Escherichia coli nucleoids during chromosome partitioning.

    abstract::We show the intracellular localization of the Escherichia coli replication origin (oriC) and chromosome terminus during the cell division cycle by FISH. In newborn cells, oriC is localized at the old-pole-proximal nucleoid border and the terminus at the new-pole-proximal nucleoid border. One copy of replicated oriC mi...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.12.7.1036

    authors: Niki H,Hiraga S

    更新日期:1998-04-01 00:00:00

  • Dorsoventral patterning in the Drosophila central nervous system: the intermediate neuroblasts defective homeobox gene specifies intermediate column identity.

    abstract::One of the first steps in neurogenesis is the diversification of cells along the dorsoventral axis. In Drosophila the central nervous system develops from three longitudinal columns of cells: ventral cells that express the vnd/nk2 homeobox gene, intermediate cells, and dorsal cells that express the msh homeobox gene. ...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.12.22.3591

    authors: Weiss JB,Von Ohlen T,Mellerick DM,Dressler G,Doe CQ,Scott MP

    更新日期:1998-11-15 00:00:00

  • Loss of C. elegans BBS-7 and BBS-8 protein function results in cilia defects and compromised intraflagellar transport.

    abstract::Bardet-Biedl syndrome (BBS) is a genetically heterogeneous developmental disorder whose molecular basis is largely unknown. Here, we show that mutations in the Caenorhabditis elegans bbs-7 and bbs-8 genes cause structural and functional defects in cilia. C. elegans BBS proteins localize predominantly at the base of ci...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.1194004

    authors: Blacque OE,Reardon MJ,Li C,McCarthy J,Mahjoub MR,Ansley SJ,Badano JL,Mah AK,Beales PL,Davidson WS,Johnsen RC,Audeh M,Plasterk RH,Baillie DL,Katsanis N,Quarmby LM,Wicks SR,Leroux MR

    更新日期:2004-07-01 00:00:00

  • Interleukin-7 induces N-myc and c-myc expression in normal precursor B lymphocytes.

    abstract::Expression of both N-myc and c-myc is induced rapidly and dramatically in normal pre-B cells after stimulation with interleukin-7 (IL-7), a pre-B cell-specific growth factor. These IL-7-induced increases in N-myc and c-myc expression are mediated at the transcriptional level; for N-myc, a major portion of the inductio...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.6.1.61

    authors: Morrow MA,Lee G,Gillis S,Yancopoulos GD,Alt FW

    更新日期:1992-01-01 00:00:00

  • The TIR1 protein of Arabidopsis functions in auxin response and is related to human SKP2 and yeast grr1p.

    abstract::Genetic analysis in Arabidopsis has led to the identification of several genes that are required for auxin response. One of these genes, AXR1, encodes a protein related to yeast Aos1p, a protein that functions to activate the ubiquitin-related protein Smt3p. Here we report the identification of a new gene called TRANS...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.12.2.198

    authors: Ruegger M,Dewey E,Gray WM,Hobbie L,Turner J,Estelle M

    更新日期:1998-01-15 00:00:00

  • Dorsal and neural expression of a tyrosine kinase-related Drosophila gene during embryonic development.

    abstract::Sequence analysis of an embryonic transcript of Drosophila predicts a tyrosine protein kinase-related gene. The prediction is based on several protein domains that are homologous to the functional domains of kinase-related oncogenes and several serine, threonine, and tyrosine protein kinases. For this reason, we named...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.1.8.862

    authors: Haller J,Côté S,Brönner G,Jäckle H

    更新日期:1987-10-01 00:00:00

  • Cytokine rescue of p53-dependent apoptosis and cell cycle arrest is mediated by distinct Jak kinase signaling pathways.

    abstract::Exposure of hematopoietic progenitors to gamma-irradiation (IR) induces p53-dependent apoptosis and a p53-independent G2/M cell cycle arrest. These responses to DNA-damage can be inhibited by treatment with cytokine growth factors. Here we report that gamma-IR-induced apoptosis and cell cycle arrest are suppressed by ...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.12.8.1099

    authors: Quelle FW,Wang J,Feng J,Wang D,Cleveland JL,Ihle JN,Zambetti GP

    更新日期:1998-04-15 00:00:00

  • Mismatch repair-dependent processing of methylation damage gives rise to persistent single-stranded gaps in newly replicated DNA.

    abstract::O(6)-Methylguanine ((Me)G) is a highly cytotoxic DNA modification generated by S(N)1-type methylating agents. Despite numerous studies implicating DNA replication, mismatch repair (MMR), and homologous recombination (HR) in (Me)G toxicity, its mode of action has remained elusive. We studied the molecular transactions ...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.455407

    authors: Mojas N,Lopes M,Jiricny J

    更新日期:2007-12-15 00:00:00

  • The HIV-1 Tat protein activates transcription from an upstream DNA-binding site: implications for Tat function.

    abstract::The Tat protein of human immunodeficiency virus type 1 (HIV-1) activates transcription following binding to nascent trans-activation response (TAR) RNA downstream of the transcription start site. Because Tat functions when bound to RNA, and in a position-dependent manner, it has been proposed that Tat works by a novel...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.5.12b.2496

    authors: Southgate CD,Green MR

    更新日期:1991-12-01 00:00:00

  • MASTR directs MyoD-dependent satellite cell differentiation during skeletal muscle regeneration.

    abstract::In response to skeletal muscle injury, satellite cells, which function as a myogenic stem cell population, become activated, expand through proliferation, and ultimately fuse with each other and with damaged myofibers to promote muscle regeneration. Here, we show that members of the Myocardin family of transcriptional...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.179663.111

    authors: Mokalled MH,Johnson AN,Creemers EE,Olson EN

    更新日期:2012-01-15 00:00:00

  • Cellular projections from sensory hair cells form polarity-specific scaffolds during synaptogenesis.

    abstract::The assembly of a nervous system requires the extension of axons and dendrites to specific regions where they are matched with appropriate synaptic targets. Although the cues that guide long-range outgrowth have been characterized extensively, additional mechanisms are required to explain short-range guidance in neura...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.259838.115

    authors: Dow E,Siletti K,Hudspeth AJ

    更新日期:2015-05-15 00:00:00

  • APC sets the Wnt tone necessary for cerebral cortical progenitor development.

    abstract::Adenomatous polyposis coli (APC) regulates the activity of β-catenin, an integral component of Wnt signaling. However, the selective role of the APC-β-catenin pathway in cerebral cortical development is unknown. Here we genetically dissected the relative contributions of APC-regulated β-catenin signaling in cortical p...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.302679.117

    authors: Nakagawa N,Li J,Yabuno-Nakagawa K,Eom TY,Cowles M,Mapp T,Taylor R,Anton ES

    更新日期:2017-08-15 00:00:00

  • Snail blocks the cell cycle and confers resistance to cell death.

    abstract::The Snail zinc-finger transcription factors trigger epithelial-mesenchymal transitions (EMTs), endowing epithelial cells with migratory and invasive properties during both embryonic development and tumor progression. During EMT, Snail provokes the loss of epithelial markers, as well as changes in cell shape and the ex...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.294104

    authors: Vega S,Morales AV,Ocaña OH,Valdés F,Fabregat I,Nieto MA

    更新日期:2004-05-15 00:00:00

  • A genome-wide RNAi screen identifies multiple RSK-dependent regulators of cell migration.

    abstract::To define the functional pathways regulating epithelial cell migration, we performed a genome-wide RNAi screen using 55,000 pooled lentiviral shRNAs targeting ∼11,000 genes, selecting for transduced cells with increased motility. A stringent validation protocol generated a set of 31 genes representing diverse pathways...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.1989110

    authors: Smolen GA,Zhang J,Zubrowski MJ,Edelman EJ,Luo B,Yu M,Ng LW,Scherber CM,Schott BJ,Ramaswamy S,Irimia D,Root DE,Haber DA

    更新日期:2010-12-01 00:00:00

  • HBP1: a HMG box transcriptional repressor that is targeted by the retinoblastoma family.

    abstract::A prominent feature of cell differentiation is the initiation and maintenance of an irreversible cell cycle arrest with the complex involvement of the retinoblastoma (RB) family (RB, p130, p107). We have isolated the HBP1 transcriptional repressor as a potential target of the RB family in differentiated cells. By homo...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.11.3.383

    authors: Tevosian SG,Shih HH,Mendelson KG,Sheppard KA,Paulson KE,Yee AS

    更新日期:1997-02-01 00:00:00

  • Human TAFII250 interacts with RAP74: implications for RNA polymerase II initiation.

    abstract::Accurate and regulated transcription by RNA polymerase II requires the assembly of an initiation complex involving multiple protein-DNA and protein-protein interactions. A key event is binding of TFIID, a complex consisting of TBP and associated factors (TAFs) to the template DNA. The TAF subunits of TFIID carry out d...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.9.22.2747

    authors: Ruppert S,Tjian R

    更新日期:1995-11-15 00:00:00

  • Hap2-Ino80-facilitated transcription promotes de novo establishment of CENP-A chromatin.

    abstract::Centromeres are maintained epigenetically by the presence of CENP-A, an evolutionarily conserved histone H3 variant, which directs kinetochore assembly and hence centromere function. To identify factors that promote assembly of CENP-A chromatin, we affinity-selected solubilized fission yeast CENP-ACnp1 chromatin. All ...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.332536.119

    authors: Singh PP,Shukla M,White SA,Lafos M,Tong P,Auchynnikava T,Spanos C,Rappsilber J,Pidoux AL,Allshire RC

    更新日期:2020-02-01 00:00:00

  • Functional analysis and in vivo footprinting implicate the erythroid transcription factor GATA-1 as a positive regulator of its own promoter.

    abstract::Transcription of erythroid-expressed genes and normal erythroid development in vivo are dependent on a regulatory protein (GATA-1) that recognizes a consensus GATA motif. GATA-1 expression is itself restricted to erythroid progenitors and to two related hematopoietic lineages, megakaryocytes and mast cells. During cel...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.5.6.919

    authors: Tsai SF,Strauss E,Orkin SH

    更新日期:1991-06-01 00:00:00

  • Autoregulation of TDP-43 mRNA levels involves interplay between transcription, splicing, and alternative polyA site selection.

    abstract::TDP-43 is a critical RNA-binding factor associated with pre-mRNA splicing in mammals. Its expression is tightly autoregulated, with loss of this regulation implicated in human neuropathology. We demonstrate that TDP-43 overexpression in humans and mice activates a 3' untranslated region (UTR) intron, resulting in exci...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.194829.112

    authors: Avendaño-Vázquez SE,Dhir A,Bembich S,Buratti E,Proudfoot N,Baralle FE

    更新日期:2012-08-01 00:00:00

  • p53 is essential for DNA methylation homeostasis in naïve embryonic stem cells, and its loss promotes clonal heterogeneity.

    abstract::DNA methylation is a key regulator of embryonic stem cell (ESC) biology, dynamically changing between naïve, primed, and differentiated states. The p53 tumor suppressor is a pivotal guardian of genomic stability, but its contributions to epigenetic regulation and stem cell biology are less explored. We report that, in...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.299198.117

    authors: Tovy A,Spiro A,McCarthy R,Shipony Z,Aylon Y,Allton K,Ainbinder E,Furth N,Tanay A,Barton M,Oren M

    更新日期:2017-05-15 00:00:00

  • Suppression of a cold-sensitive mutation in 16S rRNA by overexpression of a novel ribosome-binding factor, RbfA.

    abstract::A novel 15-kDa protein, RbfA, has been identified by virtue of its ability to act as a high copy suppressor of a previously characterized dominant cold-sensitive mutation (C23U) in 16S rRNA. RbfA is found associated with free 30S ribosomal subunits, but not with 70S ribosomes or polysomes, and is essential for maximal...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.9.5.626

    authors: Dammel CS,Noller HF

    更新日期:1995-03-01 00:00:00

  • A weak germ-line excision mutation blocks developmentally controlled amplification of the rDNA minichromosome of Tetrahymena thermophila.

    abstract::During development of the somatic macronucleus of Tetrahymena thermophila, the rDNA is excised from its germ-line chromosome, rearranged into a palindrome, and amplified to 10(4) copies. We have identified a cis-acting germ-line mutation, rmm11/6, that prevents amplification of the rDNA in all but approximately 1 in 1...

    journal_title:Genes & development

    pub_type: 杂志文章

    doi:10.1101/gad.8.1.84

    authors: Kapler GM,Blackburn EH

    更新日期:1994-01-01 00:00:00