A Database of Drosophila Genes & Genomes

FB2012_01, released January 20th, 2012
 

Dmel\P{GawB}apmd544 Insertion

General Information
Symbol Dmel\P{GawB}apmd544 Species D. melanogaster
Name FlyBase ID FBti0002785
Feature type transposable_element_insertion_site
Description
Inserted element P{GawB} Expression data GAL4 reporter/driver
Affected gene(s) ap, Scer\GAL4 Viability / fertility
Causes allele(s) apmd544, Scer\GAL4ap-md544 Stock availability 2 publicly available
LINE ID
Genomic Location
Chromosomal location 2R ( 41F8 ) Sequence location
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Description
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FB2011_10
References
FB2012_01
References
All updates Click here to see a list of all updates to this record from FB2010_08 and on.
hide Detailed Mapping Data
Chromosome (arm)
Sequence Location
Orientation
Cytological location
(computed by FlyBase)
41F8 ( near gene of known cytology )
Cytological location
(reported)
Comments concerning
location
hide Sequence Data
Flanking sequence
hide Inserted Element
Construct P{GawB}
Location-dependent
role
GAL4 driver/enhancer trap
Size 11.279Kb
Associated alleles
Molecular map
hide Affected Gene(s)
Insertion may
affect gene
(Hughes and Fehon, 2006, Yan et al., 2009, Evans et al., 2009, Glise et al., 2005, Li et al., 2006, Stabell et al., 2006, Calleja, 1996.10.16, Bonkowsky et al., 1999, Orihara-Ono et al., 2005, Cha et al., 2005, del Alamo Rodriguez et al., 2002, Dearborn et al., 2002, Milan and Cohen, 1999, Milan and Cohen, 1999, True et al., 1999, Piddini et al., 2005, Nagel et al., 2001, Radimerski et al., 2002, Hewes et al., 2003, Teleman and Cohen, 2006, Montagne et al., 1999, Moreno and Morata, 1999, Keleman and Dickson, 2001, Takeo et al., 2005, Rintelen et al., 2001, Allan et al., 2003, Vanolst et al., 2005, Villa-Cuesta and Modolell, 2005, Weihe et al., 2001, Niwa et al., 2002, Paricio et al., 1999, Yoshida et al., 2001, Herzig et al., 2001, Pena-Rangel et al., 2002, Hidalgo et al., 2001, Greco et al., 2001, van Meyel et al., 2003, Feiguin et al., 2001, Milan et al., 2001, Friedman and Perrimon, 2006, Delanoue et al., 2002, Cavodeassi et al., 2002, Wulbeck and Simpson, 2002, de Navas et al., 2006, Takaesu et al., 2005, Stabell et al., 2006, Milan and Cohen, 2003, Giagtzoglou et al., 2003, Hannus et al., 2002, Ratnaparkhi et al., 2002, Okajima and Irvine, 2002, Speck et al., 2003, Giraldez et al., 2002, Barcelo and Stewart, 2002, Enerly et al., 2002, Hennig and Neufeld, 2002, Garcia-Casado et al., 2002, Price et al., 2002, Giraldez et al., 2002, Azpiazu and Morata, 2002, Callus and Mathey-Prevot, 2002, Matakatsu and Blair, 2004, Milan et al., 2004, Lohr et al., 2002, Nakamura et al., 2002, Fradkin et al., 2004, Copf et al., 2003, Stevaux et al., 2002, Resino and Garcia-Bellido, 2004, Takeo et al., 2004, Fan et al., 2003, Pfeiffer et al., 2002, Weihe et al., 2004, Adachi-Yamada and O'Connor, 2002, Denef et al., 2000, Conley et al., 2000, Park et al., 2004, Calleja et al., 2000, Marques et al., 2003, Campbell and Tomlinson, 2000, Giraldez and Cohen, 2003, Baena-Lopez et al., 2003, Escudero et al., 2003, Horabin et al., 2003, Rincon-Limas et al., 2000, O'Keefe and Thomas, 2001, Nolo et al., 2000, Seher and Leptin, 2000, Tanimoto et al., 2000, Milan and Cohen, 2000, Pueyo et al., 2000, Collins and Treisman, 2000, Culi et al., 2001, Simpson et al., 2000, Rajagopalan et al., 2000, Boutros et al., 2000, Azpiazu and Morata, 2000, Kojima et al., 2000, Lu et al., 1999, Zeitlinger and Bohmann, 1999, van Meyel et al., 1999, Gao et al., 2000, van Meyel et al., 2000, Benveniste et al., 1998, Hepker et al., 1999, Royet et al., 1998, Vervoort et al., 1999, Pickup and Banerjee, 1999, Diez del Corral et al., 1999, Bishop et al., 1999, Rincon-Limas et al., 1999, Ligoxygakis et al., 1999, Ting et al., 2005, Sato et al., 1999, Aldaz et al., 2005, Escudero et al., 2005, Zeng and Verheyen, 2004, Ruiz-Gomez et al., 2000, Methot and Basler, 2000, Lu et al., 2000, Gorfinkiel et al., 1997, Baeg et al., 2004, Pueyo and Couso, 2004, Merdes et al., 2004, Nakano et al., 2004, Perez-Garijo et al., 2004, Miguel-Aliaga et al., 2004, Martin et al., 2004, Kirkpatrick et al., 2004, Marquez et al., 2001, Mihaly et al., 2001, Fernandez-Funez et al., 1998, Mishra et al., 2001, Cho et al., 2001, O'Keefe et al., 1998, Kiger and O'Shea, 2001, Milan et al., 1998, Kango-Singh et al., 2003, Chandra et al., 2003, Chen et al., 2002, Patel et al., 2003, Vegh and Basler, 2003, Allan et al., 2003, Pallavi and Shashidhara, 2003, Milan et al., 1997, Aldaz et al., 2003, Wheeler et al., 2003, Bernard et al., 2003, Villa-Cuesta et al., 2003, Yang et al., 2003, Apidianakis et al., 1999, Kreuger et al., 2004, Gorfinkiel et al., 2005, Horabin, 2005, Matakatsu and Blair, 2006, Bischof et al., 2007, Biryukova and Heitzler, 2005, Cha et al., 2003, Soller et al., 2006, Baena-Lopez and Garcia-Bellido, 2006, Wei et al., 2005, Crickmore and Mann, 2006, Crickmore and Mann, 2006, Oshima, 2006, Blair et al., 2006, Jacobsen et al., 2006, Ramel, 2007, Bischof et al., 2007, Baumgardt et al., 2007, Hyun et al., 2006, Garbe et al., 2007, Hulsmeier et al., 2007, Chung et al., 2007, Secombe et al., 2007, He et al., 2005, He et al., 2005, Stabell et al., 2007, Staudt et al., 2006, Miura et al., 2006, Bardin and Schweisguth, 2006, Wu et al., 2005, Hewes et al., 2006, David et al., 2005, Krieser et al., 2007, Kiger et al., 2007, Park et al., 2008, Markstein et al., 2008, Callejo et al., 2006, Bejarano et al., 2008, Mouchel-Vielh et al., 2008, Yan et al., 2008, Carrera et al., 2008, Gluderer et al., 2008, Schwinkendorf and Gallant, 2009, Moores et al., 2008, Miura et al., 2008, Ueyama et al., 2008, Kim et al., 2007, Zeng et al., 2007, Montero et al., 2008, Jang et al., 2008, Steiger et al., 2008, Hijazi et al., 2009, Yang et al., 2005, Lee et al., 2006, Ayers et al., 2009, Schlichting and Dahmann, 2008, Loewer et al., 2004, Eivers et al., 2009, Zirin and Mann, 2007, Lee et al., 2009, Khaliullina et al., 2009, Morris et al., 2006, Guha et al., 2009, Biryukova and Heitzler, 2008, Bejarano et al., 2007, Johnson et al., 2008, Herranz et al., 2006, Gallet et al., 2008, Bejarano et al., 2010, Yan et al., 2009, Widmann and Dahmann, 2009, Usha and Shashidhara, 2010, Baumgartner et al., 2010, Hermle et al., 2010, Jones et al., 2010, Yang et al., 2009, Cheng et al., 2010, Buechling et al., 2010, Djiane and Mlodzik, 2010, Lee et al., 2010, Yan et al., 2010, Franch-Marro et al., 2008, Jia et al., 2009, Baumgardt et al., 2009, Losada-Pérez et al., 2010, Morton et al., 2008, Rhiner et al., 2010, Lu et al., 2010, Kleinschmit et al., 2010, de Haro et al., 2010, Padash-Barmchi et al., 2010, Zhang et al., 2006, Ellis and Carney, 2011, Kondo and Perrimon, 2011, Furrer et al., 2010, Mesquita et al., 2010, Tortoriello et al., 2010, Bronstein et al., 2010, O'Keefe et al., 2011, Morante et al., 2011, Terriente-Félix et al., 2011, Molnar et al., 2011, Song et al., 2010, Resnik-Docampo and de Celis, 2011, Kawamori and Yamaguchi, 2011, Fernández et al., 2011, Hijazi et al., 2011, Montagne et al., 2010, Loncle et al., 2007, Liu et al., 2011, Wojcinski et al., 2011, Du et al., 2011, Gemmill et al., 2002, Hamanaka et al., 2010, Jia et al., 2010, Riedel et al., 2011, Tripura et al., 2011, Franke et al., 2010, Hughes et al., 2010, Keleman et al., 2005, Coleman et al., 2010, Xie et al., 2011, Xie et al., 2010, Deng et al., 2010, Zamparini et al., 2011)
hide Alleles and Phenotypes
Causes alleles
(Calleja, 1996.10.16, Hughes and Fehon, 2006, Bonkowsky et al., 1999, Yan et al., 2009, Orihara-Ono et al., 2005, Cha et al., 2005, del Alamo Rodriguez et al., 2002, Dearborn et al., 2002, Milan and Cohen, 1999, Milan and Cohen, 1999, True et al., 1999, Piddini et al., 2005, Nagel et al., 2001, Radimerski et al., 2002, Hewes et al., 2003, Teleman and Cohen, 2006, Montagne et al., 1999, Moreno and Morata, 1999, Keleman and Dickson, 2001, Takeo et al., 2005, Rintelen et al., 2001, Allan et al., 2003, Vanolst et al., 2005, Villa-Cuesta and Modolell, 2005, Weihe et al., 2001, Niwa et al., 2002, Paricio et al., 1999, Yoshida et al., 2001, Herzig et al., 2001, Pena-Rangel et al., 2002, Hidalgo et al., 2001, Greco et al., 2001, van Meyel et al., 2003, Feiguin et al., 2001, Milan et al., 2001, Friedman and Perrimon, 2006, Delanoue et al., 2002, Evans et al., 2009, Cavodeassi et al., 2002, Wulbeck and Simpson, 2002, de Navas et al., 2006, Takaesu et al., 2005, Stabell et al., 2006, Milan and Cohen, 2003, Giagtzoglou et al., 2003, Hannus et al., 2002, Ratnaparkhi et al., 2002, Okajima and Irvine, 2002, Speck et al., 2003, Giraldez et al., 2002, Barcelo and Stewart, 2002, Enerly et al., 2002, Hennig and Neufeld, 2002, Garcia-Casado et al., 2002, Price et al., 2002, Giraldez et al., 2002, Azpiazu and Morata, 2002, Callus and Mathey-Prevot, 2002, Matakatsu and Blair, 2004, Milan et al., 2004, Lohr et al., 2002, Nakamura et al., 2002, Fradkin et al., 2004, Copf et al., 2003, Stevaux et al., 2002, Resino and Garcia-Bellido, 2004, Takeo et al., 2004, Fan et al., 2003, Pfeiffer et al., 2002, Weihe et al., 2004, Adachi-Yamada and O'Connor, 2002, Denef et al., 2000, Conley et al., 2000, Park et al., 2004, Calleja et al., 2000, Marques et al., 2003, Campbell and Tomlinson, 2000, Giraldez and Cohen, 2003, Baena-Lopez et al., 2003, Escudero et al., 2003, Horabin et al., 2003, Rincon-Limas et al., 2000, O'Keefe and Thomas, 2001, Nolo et al., 2000, Seher and Leptin, 2000, Tanimoto et al., 2000, Milan and Cohen, 2000, Glise et al., 2005, Pueyo et al., 2000, Collins and Treisman, 2000, Culi et al., 2001, Simpson et al., 2000, Rajagopalan et al., 2000, Boutros et al., 2000, Azpiazu and Morata, 2000, Kojima et al., 2000, Lu et al., 1999, Zeitlinger and Bohmann, 1999, van Meyel et al., 1999, Gao et al., 2000, van Meyel et al., 2000, Benveniste et al., 1998, Hepker et al., 1999, Royet et al., 1998, Vervoort et al., 1999, Pickup and Banerjee, 1999, Diez del Corral et al., 1999, Bishop et al., 1999, Rincon-Limas et al., 1999, Ligoxygakis et al., 1999, Ting et al., 2005, Sato et al., 1999, Aldaz et al., 2005, Escudero et al., 2005, Zeng and Verheyen, 2004, Ruiz-Gomez et al., 2000, Methot and Basler, 2000, Lu et al., 2000, Gorfinkiel et al., 1997, Baeg et al., 2004, Pueyo and Couso, 2004, Merdes et al., 2004, Nakano et al., 2004, Perez-Garijo et al., 2004, Miguel-Aliaga et al., 2004, Martin et al., 2004, Kirkpatrick et al., 2004, Marquez et al., 2001, Mihaly et al., 2001, Fernandez-Funez et al., 1998, Mishra et al., 2001, Cho et al., 2001, O'Keefe et al., 1998, Kiger and O'Shea, 2001, Milan et al., 1998, Kango-Singh et al., 2003, Chandra et al., 2003, Chen et al., 2002, Patel et al., 2003, Vegh and Basler, 2003, Allan et al., 2003, Pallavi and Shashidhara, 2003, Milan et al., 1997, Aldaz et al., 2003, Wheeler et al., 2003, Bernard et al., 2003, Villa-Cuesta et al., 2003, Yang et al., 2003, Apidianakis et al., 1999, Kreuger et al., 2004, Gorfinkiel et al., 2005, Horabin, 2005, Matakatsu and Blair, 2006, Bischof et al., 2007, Biryukova and Heitzler, 2005, Cha et al., 2003, Soller et al., 2006, Baena-Lopez and Garcia-Bellido, 2006, Wei et al., 2005, Crickmore and Mann, 2006, Crickmore and Mann, 2006, Oshima, 2006, Blair et al., 2006, Jacobsen et al., 2006, Ramel, 2007, Stabell et al., 2006, Li et al., 2006, Bischof et al., 2007, Baumgardt et al., 2007, Hyun et al., 2006, Garbe et al., 2007, Hulsmeier et al., 2007, Chung et al., 2007, Secombe et al., 2007, He et al., 2005, He et al., 2005, Stabell et al., 2007, Staudt et al., 2006, Miura et al., 2006, Bardin and Schweisguth, 2006, Wu et al., 2005, Hewes et al., 2006, David et al., 2005, Krieser et al., 2007, Kiger et al., 2007, Park et al., 2008, Markstein et al., 2008, Callejo et al., 2006, Bejarano et al., 2008, Mouchel-Vielh et al., 2008, Yan et al., 2008, Carrera et al., 2008, Gluderer et al., 2008, Schwinkendorf and Gallant, 2009, Moores et al., 2008, Miura et al., 2008, Ueyama et al., 2008, Kim et al., 2007, Zeng et al., 2007, Montero et al., 2008, Jang et al., 2008, Steiger et al., 2008, Hijazi et al., 2009, Yang et al., 2005, Lee et al., 2006, Ayers et al., 2009, Schlichting and Dahmann, 2008, Loewer et al., 2004, Eivers et al., 2009, Zirin and Mann, 2007, Lee et al., 2009, Khaliullina et al., 2009, Morris et al., 2006, Guha et al., 2009, Biryukova and Heitzler, 2008, Bejarano et al., 2007, Johnson et al., 2008, Herranz et al., 2006, Gallet et al., 2008, Bejarano et al., 2010, Yan et al., 2009, Widmann and Dahmann, 2009, Usha and Shashidhara, 2010, Baumgartner et al., 2010, Hermle et al., 2010, Jones et al., 2010, Yang et al., 2009, Cheng et al., 2010, Buechling et al., 2010, Djiane and Mlodzik, 2010, Lee et al., 2010, Yan et al., 2010, Franch-Marro et al., 2008, Jia et al., 2009, Baumgardt et al., 2009, Losada-Pérez et al., 2010, Morton et al., 2008, Rhiner et al., 2010, Lu et al., 2010, Kleinschmit et al., 2010, de Haro et al., 2010, Padash-Barmchi et al., 2010, Zhang et al., 2006, Ellis and Carney, 2011, Kondo and Perrimon, 2011, Furrer et al., 2010, Mesquita et al., 2010, Tortoriello et al., 2010, Bronstein et al., 2010, O'Keefe et al., 2011, Morante et al., 2011, Terriente-Félix et al., 2011, Molnar et al., 2011, Song et al., 2010, Resnik-Docampo and de Celis, 2011, Kawamori and Yamaguchi, 2011, Fernández et al., 2011, Hijazi et al., 2011, Montagne et al., 2010, Loncle et al., 2007, Liu et al., 2011, Wojcinski et al., 2011, Du et al., 2011, Gemmill et al., 2002, Hamanaka et al., 2010, Jia et al., 2010, Riedel et al., 2011, Tripura et al., 2011, Franke et al., 2010, Hughes et al., 2010, Keleman et al., 2005, Coleman et al., 2010, Xie et al., 2011, Xie et al., 2010, Deng et al., 2010, Zamparini et al., 2011)
Lethality
References
Sterility
References
sterile | recessive
hide Phenotype Manifest In
embryonic/larval neuron
embryonic deuterocerebrum
embryonic protocerebrum
interneuron | embryonic stage
longitudinal connective
presumptive embryonic/larval central nervous system
wing | heat sensitive
wing disc | dorsal/ventral compartment boundary
wing margin bristle
hide Detailed Description
Statement
Reference
Flies expressing fng[Scer\UAS.cKa] under the control of Scer\GAL4[ap-md544] in a ap[rK568]/ap[md544] background have ventralised halteres. In addition, the halteres form dark-pigmented bristles that are similar to those formed at the wing margin.
Bx[1]/Y ; ap[md544]/+ males have a strong wing scalloping phenotype.
apmd544/+ enhances the severity of the Bx1 wing scalloping phenotype.
apmd544/+ does not cause any visible leg phenotypes in combination with Chig371/+, Chig96.1/+ or Chie5.5/+. ap::ChiΔLID.ΔLIM.Scer\UAS.T:Hsap\MYC; Scer\GAL4ap-md544 suppresses fusion of tarsal segments 4 and 5 in apUGO35/apmd544 flies. ap::Lim3Scer\UAS.cOa; Scer\GAL4ap-md544 suppresses fusion of tarsal segments 4 and 5 in apUGO35/apmd544 flies.
In apUGO35/apmd544 and in apmd544/Df(2R)nap1 flies, the fourth tarsal segment is almost completely lost. The remnant is fused to the fifth tarsal segment. Other segments are normal.
Reduction and fusion of the fourth tarsal segment in apmd544/Df(2R)nap1 animals is rescued by apScer\UAS.cOa.
Mutant animals show a weak phenotype in the wing disc, the dorsal ventral affinity boundary is disrupted. The phenotype is stronger in aprK568/apmd544 animals and stronger still with apUGO35/apmd544.
Neurons which normally express ap (Ap neurons) are still present and extend axons in apP44/apmd544 embryonic brains. However, Ap brain interneurons show defasciculation and pathfinding defects in these animals. The most severe defects are seen in the deutocerebrum, where the two pairs of Ap neuronal cell bodies are positioned incorrectly. These neurons do not appear to undergo the movements seen in wild-type embryos and never become localised on the inner surface of the developing deutocerebrum, instead remaining on the outer surface, with their axons projecting aberrantly along the frontal commissure of the stomatogastric nervous system or in rare cases along the recurrent nerve. The cell bodies of the Ap neurons in the protocerebrum appear to be positioned properly and have a normal size and shape, but many of their commissural axons fail to form commissural fascicles correctly and often leave their commissural bundle and cross over to grow along a neighbouring fascicle. This defect is seen in 30% of cases. Ap neurons that innervate the ring gland have normal axonal projection patterns. Fas2-expressing commissural fascicles are indistinguishable from wild type.
Expression of DrScer\UAS.cIa under the control of Scer\GAL4ap-md544 in apmd544/apUGO35 flies does not restore outgrowth of the wing, although the few margin bristles seen in the dorsal surface of these wings have dorsal identity. Growth of the wing and wing margin formation can be restored in apmd544/apUGO35 flies expressing fngEP3082 under the control of Scer\GAL4ap-md544. Both surfaces of the wing differentiate ventral structures; the anterior wing margin and alula differentiate ventral bristles on both surfaces and the pattern of vein corrugation is ventral. Co-expression of fngEP3082 and DrScer\UAS.cIa under the control of Scer\GAL4ap-md544 in apmd544/apUGO35 flies results in dorsal differentiation in bristles of the dorsal anterior wing margin.
Expression of capsScer\UAS.cSa under the control of Scer\GAL4ap-md544 restores the smooth interface between dorsal and ventral cells in apmd544/apUGO35 wing discs. The boundary between the dorsal and ventral cells is still irregular in apmd544/apUGO35 wing discs expressing trnScer\UAS.cMa under the control of Scer\GAL4ap-md544. Expression of ConScer\UAS.cRa or fngEP3082 under the control of Scer\GAL4ap-md544 does not restore a smooth boundary between the dorsal and ventral cells in apmd544/apUGO35 wing discs.
The wing margin is reduced and the wing is considerably smaller than normal in apmd544/apUGO35 flies. When present, wing margin bristles have ventral identity.
apmd544/apUGO35 wing discs do not form a smooth boundary between dorsal and ventral cells.
A sharp boundary between dorsal and ventral cells is restored in aprK568/apmd544 wing discs expressing fngScer\UAS.cKa under the control of Scer\GAL4ap-md544. No violations of the compartment boundary are seen. The resulting adult flies have wings of roughly normal size with clearly demarcated wing margin. The rescued wing margin is ventralised; dorsal-specific sensory bristles are completely missing along the anterior margin and cells on both sides of the margin secrete ventral bristle types. The dorsal and ventral wing surfaces are not adhered to each other, resulting in a balloon-like structure. apUGO35/apmd544 flies expressing fngScer\UAS.cKa under the control of Scer\GAL4ap-md544 do not have wing margin defects. Coexpression of mewScer\UAS.cWa and fngScer\UAS.cKa under the control of Scer\GAL4ap-md544 partially rescues the apts78j/apmd544 wing phenotype; the overall size and shape, apposition of the two surfaces, position of the wing margin and pattern of the wing veins are remarkably normal. However, these wings consist entirely of ventral cell types. Firstly, the rescued wing margins lack the dorsal-specific bristles types and instead have ventral bristle types on both surfaces. Secondly, the wings have many more alula bristles than normal (which in wild-type are derived only from the ventral surface). Thirdly, a mechanosensory campaniform sensillum that is normally located only on the ventral surface of vein L3 is duplicated and present on both surfaces of the rescued wing. Finally, the morphology of the wing veins indicate that they entirely of ventral identity (the veins show a ventral corrugation pattern on both surfaces of the wing).
The D/V compartment boundary of aprK568/apmd544 wing discs is highly irregular (in contrast to wild type). The resulting adult wings are almost completely eliminated and show no evidence of a wing margin. apts78j/apmd544 flies show a nearly complete loss of wings at 25oC.
A sharp boundary between dorsal and ventral cells is restored in aprK568/apmd544 wing discs expressing fngScer\UAS.cKa under the control of Scer\GAL4ap-md544. No violations of the compartment boundary are seen. The resulting adult flies have wings of roughly normal size with clearly demarcated wing margin. The rescued wing margin is ventralised; dorsal-specific sensory bristles are completely missing along the anterior margin and cells on both sides of the margin secrete ventral bristle types. The dorsal and ventral wing surfaces are not adhered to each other, resulting in a balloon-like structure. apUGO35/apmd544 flies expressing fngScer\UAS.cKa under the control of Scer\GAL4ap-md544 do not have wing margin defects. Coexpression of mewScer\UAS.cWa and fngScer\UAS.cKa under the control of Scer\GAL4ap-md544 partially rescues the apts78j/apmd544 wing phenotype; the overall size and shape, apposition of the two surfaces, position of the wing margin and pattern of the wing veins are remarkably normal. However, these wings consist entirely of ventral cell types. Firstly, the rescued wing margins lack the dorsal-specific bristles types and instead have ventral bristle types on both surfaces. Secondly, the wings have many more alula bristles than normal (which in wild-type are derived only from the ventral surface). Thirdly, a mechanosensory campaniform sensillum that is normally located only on the ventral surface of vein L3 is duplicated and present on both surfaces of the rescued wing. Finally, the morphology of the wing veins indicate that they are entirely of ventral identity (the veins show a ventral corrugation pattern on both surfaces of the wing).
apmd544/apUGO35 fail to develop normal wings.
Transheterozygotes with Df(2R)nap1 show fusion of tarsus 4 with 5, reduction and deformity or loss of tarsus 4. Tarsus four and five fusions appear with lower frequency and expressivity in apUGO35/apmd544 transheterozygotes.
apmd544/apUGO35 flies have immature ovaries, are sterile, die within 24-72 hours of eclosion and have no wings. apmd544/apts78j flies grown at 25oC have wings that lack most of the wing margin but have good proximo-distal growth. apmd544/apts78j flies grown at 25oC have wings that lack most of the wing margin but have good proximo-distal growth. The addition of apHA-B.Scer\UAS severely reduces proximo-distal growth and wing size.
In apmd544/apP44 embryos, all neurons that normally express ap survive and extend axons, but these axons display pathfinding errors in nearly every segment, including defasciculation of axon bundles, aberrant pathway selection within the longitudinal connectives, occasional misrouting across the midline and stalling.
No increase in axon guidance defects is seen in apmd544/Chie5.5 transheterozygotes compared to apmd544/+ or Chie5.5/+ embryos. ap::ChiΔLID.ΔLIM.Scer\UAS.T:Hsap\MYC rescues pathway recognition and axon fasciculation in a majority of segments in apmd544/apP44 embryos when expressed under the control of Scer\GAL4ap-md544. The axon guidance defects seen in apmd544/apP44 embryos are not rescued by coexpression of apΔLIM.Scer\UAS and ChiΔLID.Scer\UAS.T:Hsap\MYC under the control of Scer\GAL4ap-md544. The axon defects seen in Chie5.5 apmd544/apP44 double mutants are completely rescued by ap::ChiΔLID.ΔLIM.Scer\UAS.T:Hsap\MYC expressed under the control of Scer\GAL4ap-md544.
apmd544/apP44 flies show wing defects. This phenotype is suppressed by expression of apScer\UAS.cMa or ap::ChiChAp.Scer\UAS under the control of Scer\GAL4ap-md544.
apmd544/apUGO35 flies show reduction of the wing and complete loss of wing margin. apmd544/apUGO35 wing discs have small wing pouches.
Expression of SerScer\UAS.cSa under the control of Scer\GAL4ap-md544 in apmd544/apUGO35 flies restores the wing margin and supports growth of the wing. Patches of ectopic wing margin are found in both surfaces of the rescued wings and overgrowth of the wing can be seen. Expression of fngEP3082 under the control of Scer\GAL4ap-md544 rescues the phenotype of apmd544/apUGO35 flies. Patches of ectopic wing margin form and can be associated with outgrowth of the wing. Groups of cells appear to violate the dorsoventral boundary in apmd544/apUGO35 wing discs which are also expressing SerScer\UAS.cSa under the control of Scer\GAL4ap-md544. The mispositioned patches of dorsal or ventral cells form relatively smooth interfaces with surrounding cells. Cells appear to violate the dorsoventral boundary in apmd544/apUGO35 wing discs which are also expressing fngEP3082 under the control of Scer\GAL4ap-md544. Expression of both SerScer\UAS.cSa and fngEP3082 under the control of Scer\GAL4ap-md544 in apmd544/apUGO35 flies results in well-developed wings which differentiate ventral features on both surfaces; the wing margin, veins and sense organs on the topologically dorsal surface have exclusively ventral identity.
apmd544/apUGO35 flies lack wings, halteres and the scutellum region of the notum. The flies are sterile and have a lifespan of 1-3 days after eclosion.
apmd544/apUGO35 flies rescued by the expression of Hsap\LHX2Scer\UAS.cRa under the control of Scer\GAL4ap-md544 often develop one to two extra bristles in the scutellum. The phenotypes of apmd544/apUGO35 flies are rescued by Hsap\LHX2Scer\UAS.cRa expressed under the control of Scer\GAL4ap-md544. apmd544/apUGO35 flies rescued by the expression of Hsap\LHX2Scer\UAS.cRa under the control of Scer\GAL4ap-md544 often develop one to two extra bristles in the scutellum.
Heterozygotes have no wing defects. apmd544/apP44 flies have no wings but often have a ribbon- or nub-like outgrowth that lacks any recognisable structures.
apP44/apmd544 embryos show proper positioning of the thoracic ventrolateral clusters in the central nervous system and their axonal bundles appear normal.
Lim3Scer\UAS.cOa expressed under the control of Scer\GAL4ap-md544 partially rescues both the wing and embryonic central nervous system phenotype of apmd544/apP44 animals at 18oC and 25oC respectively. The wing, sterility and uncoordinated behaviour phenotypes of apmd544/apP44 flies are rescued by ap::Lim3Scer\UAS.cOa expressed under the control of Scer\GAL4ap-md544 to the same extent as the rescue seen by apScer\UAS.cOa. In contrast, the axon pathfinding phenotype of apmd544/apP44 embryos is only partially rescued by ap::Lim3Scer\UAS.cOa expressed under the control of Scer\GAL4ap-md544.
apmd544/apP44 flies have no wings, although they often have a ribbon-like outgrowth in the wing region that lacks any recognisable structures. Homozygous adults are sterile, uncoordinated and have a reduced lifespan. Axon pathfinding errors are seen in the central nervous system of apmd544/apP44 embryos; neurons that normally express ap wander within the longitudinal connective and fail to fasciculate with one another. apmd544/apts78j flies have defective wing margins and unfused wing surfaces at 18oC. Introduction of apΔHD.Scer\UAS into this background (expressed under the control of Scer\GAL4ap-md544) eliminates the wing blade altogether.
A single copy of apScer\UAS.cOa expressed under the control of Scer\GAL4ap-md544 almost completely rescues the wing phenotype of apmd544/apP44 flies; the wing blade is normal in size, with a normal margin and vein pattern, but is held at right angles away from the body. The sterility and uncoordinated behaviour phenotypes of apmd544/apP44 flies are also rescued and the central nervous system defects of embryos are rescued. The adult and embryonic phenotypes of apmd544/apP44 animals are not rescued by apΔLIM.Scer\UAS expressed under the control of Scer\GAL4ap-md544. The ribbon-like outgrowth seen in apmd544/apP44 flies is entirely eliminated in flies expressing apΔHD.Scer\UAS under the control of Scer\GAL4ap-md544.
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distribution deduced from reporter (Gal4 UAS)
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Tissue/Position (including subcellular localization)
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Marker for
dorsal mesothoracic disc
dorsal mesothoracic disc dorsal metathoracic disc
dorsal metathoracic disc
medial longitudinal fascicle
ventral thoracic disc | restricted
Reflects
expression of
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Origin as a multiple insertion line
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Balancer
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Bloomington
Kyoto
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Isolated using P{UAS-y.C} adult cuticle patterning screen; see FBrf0090484.
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Reported As
Symbol Synonym
apmd544-GAL4
apγαλ4
ap-G4
ap-Gal4
(Orihara-Ono et al., 2005, Aldaz et al., 2005, Escudero et al., 2005, Baeg et al., 2004, Perez-Garijo et al., 2004, Martin et al., 2004, Zeng and Verheyen, 2004, Escudero et al., 2003, Aldaz et al., 2003, Villa-Cuesta et al., 2003, Hewes et al., 2003, Giagtzoglou et al., 2003, Okajima and Irvine, 2002, Azpiazu and Morata, 2002, Nakamura et al., 2002, Lohr et al., 2002, Cavodeassi et al., 2002, Price et al., 2002, Rintelen et al., 2001, Culi et al., 2001, Calleja et al., 2000, Campbell and Tomlinson, 2000, Azpiazu and Morata, 2000, Tanimoto et al., 2000, Zeitlinger and Bohmann, 1999, Moreno and Morata, 1999, Vervoort et al., 1999, Bishop et al., 1999, Sato et al., 1999, Montero et al., 2008, Kreuger et al., 2004, Bischof et al., 2007, Biryukova and Heitzler, 2005, Wei et al., 2005, Crickmore and Mann, 2006, Crickmore and Mann, 2006, de Navas et al., 2006, Chung et al., 2007, Zhang et al., 2006, Bischof et al., 2007, Molnar et al., 2011, O'Keefe et al., 2011, Du et al., 2011, Bardin and Schweisguth, 2006, Hewes et al., 2006, Stabell et al., 2007, Fernández et al., 2011, Callejo et al., 2006, Yan et al., 2008, Gluderer et al., 2008, Moores et al., 2008, Yang et al., 2005, Lee et al., 2006, Loewer et al., 2004, Zirin and Mann, 2007, Guha et al., 2009, Biryukova and Heitzler, 2008, Bejarano et al., 2007, Herranz et al., 2006, Gallet et al., 2008, Bejarano et al., 2010, Yan et al., 2009, Baumgartner et al., 2010, Jones et al., 2010, Djiane and Mlodzik, 2010, Yan et al., 2010, Franch-Marro et al., 2008, Jia et al., 2009, Losada-Pérez et al., 2010, Lu et al., 2010, Kleinschmit et al., 2010, Bronstein et al., 2010, Terriente-Félix et al., 2011, Resnik-Docampo and de Celis, 2011, Montagne et al., 2010, Loncle et al., 2007, Jia et al., 2010, Xie et al., 2011, Xie et al., 2010)
ApGal4
ap-GAl4
ap-GAL4md544
ap-Gal4md544
apterous (ap)-GAL4
apterousGAL4
Apterous GAL4
apterous Gal4
Apterous Gal4
AptGal4
aptGal4
GAL4-apterous
P(GawB)apmd544
P[GawB]apmd544
P{w+mW.hs=GawB}apmd544
Secondary FlyBase IDs
  • FBti0002814
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hide Recent research papers ( 45 )
Du et al., 2011, PLoS ONE 6(9): e24168
In Vivo RNAi Screen Reveals Neddylation Genes as Novel Regulators of Hedgehog Signaling. [FBrf0215574]
Ellis and Carney, 2011, Genetics 187(1): 157--169
Socially-Responsive Gene Expression in Male Drosophila melanogaster Is Influenced by the Sex of the Interacting Partner. [FBrf0212780]
Fernández et al., 2011, Development 138(11): 2337--2346
Actin-Capping Protein and the Hippo pathway regulate F-actin and tissue growth in Drosophila. [FBrf0213674]
Hijazi et al., 2011, PLoS ONE 6(3): e17763
The ly6 protein coiled is required for septate junction and blood brain barrier organisation in Drosophila. [FBrf0213269]
Kawamori and Yamaguchi, 2011, Cell Struct. Funct. 36(1): 103--119
DREF is Critical for Drosophila Bristle Development by Regulating Endoreplication in Shaft Cells. [FBrf0213809]
Kondo and Perrimon, 2011, Sci. Signal. 4(154): rs1
A Genome-Wide RNAi Screen Identifies Core Components of the G2-M DNA Damage Checkpoint. [FBrf0212700]
Liu et al., 2011, Dev. Growth Differ. 53(6): 822--841
Negative modulation of bone morphogenetic protein signaling by Dullard during wing vein formation in Drosophila. [FBrf0214664]
Molnar et al., 2011, PLoS Genet. 7(3): e1001335
Role of the Drosophila non-visual ß-arrestin kurtz in hedgehog signalling. [FBrf0213301]
Morante et al., 2011, Development 138(4): 687--693
Cell migration in Drosophila optic lobe neurons is controlled by eyeless/Pax6. [FBrf0212874]
O'Keefe et al., 2011, Mech. Dev. 128(1-2): 59--70
EndoGI modulates Notch signaling and axon guidance in Drosophila. [FBrf0213012]
Resnik-Docampo and de Celis, 2011, PLoS ONE 6(1): e14528
MAP4K3 Is a Component of the TORC1 Signalling Complex that Modulates Cell Growth and Viability in Drosophila melanogaster. [FBrf0212911]
Riedel et al., 2011, Development 138(1): 149--158
Megalin-dependent Yellow endocytosis restricts melanization in the Drosophila cuticle. [FBrf0212536]
Terriente-Félix et al., 2011, Dev. Biol. 350(2): 382--392
A conserved function of the chromatin ATPase Kismet in the regulation of hedgehog expression. [FBrf0212899]
Tripura et al., 2011, Int. J. Dev. Biol. 55(6): 583--590
Regulation and activity of JNK signaling in the wing disc peripodial membrane during adult morphogenesis in Drosophila. [FBrf0216296]
Wojcinski et al., 2011, Dev. Biol. 358(1): 168--180
DSulfatase-1 fine-tunes Hedgehog patterning activity through a novel regulatory feedback loop. [FBrf0215253]
Xie et al., 2011, Insect Biochem. Mol. Biol. 41(3): 167--177
RNAi knockdown of dRNaseZ, the Drosophila homolog of ELAC2, impairs growth of mitotic and endoreplicating tissues. [FBrf0213094]
Zamparini et al., 2011, Development 138(18): 4039--4050
Vreteno, a gonad-specific protein, is essential for germline development and primary piRNA biogenesis in Drosophila. [FBrf0214783]
Bejarano et al., 2010, Dev. Biol. 338(1): 63--73
miR-9a prevents apoptosis during wing development by repressing Drosophila LIM-only. [FBrf0209786]
Bronstein et al., 2010, PLoS Genet. 6(8): e1001063
Transcriptional regulation by CHIP/LDB complexes. [FBrf0211594]
Buechling et al., 2010, Curr. Biol. 20(14): 1263--1268
Wnt/Frizzled Signaling Requires dPRR, the Drosophila Homolog of the Prorenin Receptor. [FBrf0211368]
Cheng et al., 2010, Dev. Biol. 337(1): 99--109
Regulation of smoothened by Drosophila G-protein-coupled receptor kinases. [FBrf0209432]
Coleman et al., 2010, Development 137(14): 2417--2426
The Adam family metalloprotease Kuzbanian regulates the cleavage of the roundabout receptor to control axon repulsion at the midline. [FBrf0211121]
de Haro et al., 2010, Cell Tissue Res. 339(2): 321--336
Detailed analysis of leucokinin-expressing neurons and their candidate functions in the Drosophila nervous system. [FBrf0209907]
Deng et al., 2010, Mol. Biol. Cell 21(19): 3304--3316
Vestigial is required during late-stage muscle differentiation in Drosophila melanogaster embryos. [FBrf0211962]
Djiane and Mlodzik, 2010, PLoS ONE 5(6): e11228
The Drosophila GIPC homologue can modulate myosin based processes and planar cell polarity but is not essential for development. [FBrf0211141]
Franke et al., 2010, Dev. Biol. 345(2): 117--132
Nonmuscle myosin II is required for cell proliferation, cell sheet adhesion and wing hair morphology during wing morphogenesis. [FBrf0211576]
Furrer et al., 2010, J. Biol. Chem. 285(51): 39623--39636
Drosophila Myc Interacts with Host Cell Factor (dHCF) to Activate Transcription and Control Growth. [FBrf0212501]
Hamanaka et al., 2010, Curr. Biol. 20(1): 9--18
Transcriptional Orchestration of the Regulated Secretory Pathway in Neurons by the bHLH protein DIMM. [FBrf0209946]
Hermle et al., 2010, Curr. Biol. 20(14): 1269--1276
Regulation of Frizzled-Dependent Planar Polarity Signaling by a V-ATPase Subunit. [FBrf0211335]
Hughes et al., 2010, J. Cell Sci. 123(7): 1099--1107
Sip1, the Drosophila orthologue of EBP50/NHERF1, functions with the sterile 20 family kinase Slik to regulate Moesin activity. [FBrf0210408]
Jia et al., 2010, J. Biol. Chem. 285(48): 37218--37226
Casein kinase 2 promotes Hedgehog signaling by regulating both smoothened and Cubitus interruptus. [FBrf0214177]
Jones et al., 2010, J. Cell Sci. 123(13): 2179--2189
Cytokinesis proteins Tum and Pav have a nuclear role in Wnt regulation. [FBrf0211056]
Kleinschmit et al., 2010, Dev. Biol. 345(2): 204--214
Drosophila heparan sulfate 6-O endosulfatase regulates Wingless morphogen gradient formation. [FBrf0211640]
Lee et al., 2010, Science 327(5970): 1223--1228
Sestrin as a feedback inhibitor of TOR that prevents age-related pathologies. [FBrf0210161]
Losada-Pérez et al., 2010, Mech. Dev. 127(9-12): 458--471
Lineage-unrelated neurons generated in different temporal windows and expressing different combinatorial codes can converge in the activation of the same terminal differentiation gene. [FBrf0212045]
Lu et al., 2010, Genetics 185(2): 549--558
The Drosophila planar polarity proteins inturned and multiple wing hairs interact physically and function together. [FBrf0211207]
Mesquita et al., 2010, PLoS Biol. 8(12): e1000566
A dp53-Dependent Mechanism Involved in Coordinating Tissue Growth in Drosophila. [FBrf0212630]
Montagne et al., 2010, PLoS Genet. 6: e1000937
The nuclear receptor DHR3 modulates dS6 kinase-dependent growth in Drosophila. [FBrf0210767]
Padash-Barmchi et al., 2010, J. Cell Sci. 123(23): 4052--4062
Control of Gliotactin localization and levels by tyrosine phosphorylation and endocytosis is necessary for survival of polarized epithelia. [FBrf0212409]
Rhiner et al., 2010, Dev. Cell 18(6): 985--998
Flower forms an extracellular code that reveals the fitness of a cell to its neighbors in Drosophila. [FBrf0211273]
Song et al., 2010, Genes Dev. 24(9): 881--886
Coop functions as a corepressor of Pangolin and antagonizes Wingless signaling. [FBrf0213249]
Tortoriello et al., 2010, FEBS J. 277(15): 3249--3263
Linking pseudouridine synthases to growth, development and cell competition. [FBrf0211423]
Usha and Shashidhara, 2010, Dev. Biol. 341(2): 389--399
Interaction between Ataxin-2 Binding Protein 1 and Cubitus-interruptus during wing development in Drosophila. [FBrf0210647]
Xie et al., 2010, Int. J. Biol. Sci. 6(3): 252--267
NIP/DuoxA is essential for Drosophila embryonic development and regulates oxidative stress response. [FBrf0211057]
Yan et al., 2010, Development 137(12): 2033--2044
The cell-surface proteins Dally-like and Ihog differentially regulate Hedgehog signaling strength and range during development. [FBrf0210906]