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The significance of responses of the genome to challenges
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Regulated splicing of the Drosophila P transposable element third intron in vitro: somatic repression
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Siebel1
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The mechanism of somatic inhibition of Drosophila P-element pre-mRNA splicing: multiprotein complexes at the exon pseudo-5′ splice site control U1 snRNP binding
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Genes Dev
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Siebel1
Fresco2
Rio3
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5
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0028146254
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Regulation of tissue-specific P-element pre-mRNA splicing requires the RNA-binding protein PSI
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The identification of P-element sequences upstream from the 5′-splice site of IVS3 that negatively regulate splicing of this intron in somatic tissue. Mutations in this region simultaneously disrupt binding of several proteins and activate splicing. Antibodies specific for a host-encoded 97 kDa protein called PSI (P-element somatic inhibitor) relieve inhibition of IVS3 splicing in somatic extracts.
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Genes Dev
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Siebel1
Kanaar2
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6
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Maternal inheritance of P cytotype in Drosophila melanogaster: a ‘pre-P cytotype’ is strictly extra-chromosomally transmitted
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Ronsseray1
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8
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0024306569
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Modified P elements that mimic the P cytotype in Drosophila melanogaster
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(1989)
Genetics
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Robertson1
Engels2
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9
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Cytotype control of Drosophila P element transposition: the 66 kd protein is a repressor of transposase activity
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(1990)
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Misra1
Rio2
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11
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0029026228
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P-element repressor autoregulation involves germ-line transcriptional repression and reduction of third intron splicing
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A study of the expression of vectors carrying the hsp83 or vasa promoter driving a coding sequence with a nuclear localization signal, a P-element fragment with exon sequences flanking IVS3 (with or without IVS3 itself), and a fused lacZ-neo reading frame. The P cytotype represses the expression of these transgenes. A correlation between level of transgene RNA and IVS3 splicing suggests a model for autoregulation of the 66 kDa protein thought to be implicated in regulation.
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Genes Dev
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Roche1
Schiff2
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Cytotype control of Drosophila melanogaster P element transposition: genomic position determines maternal repression
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Misra1
Buratowski2
Ohkawa3
Rio4
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13
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0027992609
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An env-like protein encoded by a Drosophila retroelement: evidence that gypsy is an infectious retrovirus
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This paper shows that the env-like protein of gypsy is processed similarly to retroviral env proteins. Furthermore, it demonstrates that the expression of the env-like gene of gypsy correlates with the mobilizations of gypsy and the production of infectious gypsy particles. Thus, gypsy is a functional, infectious retrovirus.
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Genes Dev
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Song1
Gerasimova2
Kurkulos3
Boeke4
Corces5
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0028053175
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Retroviruses in invertebrates: the gypsy retrotransposon is apparently an infectious retrovirus of Drosophila melanogaster
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This paper provides the first example of an infectious retrovirus in invertebrates and demonstrates the apparent infectivity of gypsy virus-like particles.
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(1994)
Proc Natl Acad Sci USA
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Kim1
Terzian2
Santamaria3
Pelisson4
Prud'homme5
Bucheton6
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16
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0028795178
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Flamenco, a gene controlling the gypsy retrovirus of Drosophila melanogaster
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The identification and genetic analysis of the locus flamenco (flam), the wild-type allele which is responsible for suppression of functional gypsy elements in stable (repressive) strains of D. melanogaster.
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(1995)
Genetics
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Prud'homme1
Gans2
Masson3
Terzian4
Bucheton5
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0028015682
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Indentification of spliced RNA species of Drosophila melanogaster gypsy retrotransposon. New evidence for retroviral nature of the gypsy element
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FEBS Lett
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Avedisov1
Ilyin2
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18
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0028110848
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Gypsy transposition correlates with the production of a retroviral envelope-like protein under the tissue-specific control of Drosophila flamenco gene
-
Describes the mechanism of regulation of gypsy expression by the flamenco (flam) gene. The results show that flam affects transcription and splicing of gypsy in a tissue-specific manner. In homozygous flam-females, gypsy is expressed at the apical poles of follicle cells and not in the oocyte. The authors put forward the hypothesis that transposition of gypsy includes infection of the oocyte by the gypsy viral particles produced in the follicle cells.
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(1994)
EMBO J
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Pelisson1
Song2
Prud'homme3
Smith4
Bucheton5
Corces6
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19
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0027296571
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Mutations at the Darkener of apricot locus modulate transcript levels of copia and copia-induced mutations in Drosophila melanogaster
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(1993)
Genetics
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Rabinow1
Chiang2
Birchler3
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20
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0028000617
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Weakener of white (Wow), a gene that modifies the expression of the white eye color locus and that suppresses position effect variegation in Drosophila melanogaster
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Mutations in Weakener of white gene (Wow), suppress position effect variegation of a euchromatic gene and enhance position effect variegation of a heterochromatic gene. Wow interacts with at least the retrotransposons copia, BEL, and B104. Mutations in Wow increase the steady state RNA level of copia in a development-dependent manner and have recessive effect on viability and fertility of flies.
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(1994)
Genetics
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Birchler1
Bhadra2
Rainbow3
Lins4
Nguyen-Huynh5
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21
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0027931653
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The Lighten up (Lip) gene of Drosophila melanogaster, a modifier of retroelement expression, position effect variegation and white locus insertion alleles
-
The Lighten up gene (Lip, 3) modifies retroelement expression, position effect variegation and white locus insertion alleles. Mutations in Lip enhance white alleles induced by insertions of the LTR retrotransposons copia, blood and coral as well as the non-LTR retrotransposon I. Lip mutations increase transcript abundance of both blood and copia and are also recessive lethal.
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(1994)
Genetics
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Csink1
Linsk2
Birchler3
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22
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0028107627
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Mosaic suppressor, a gene in Drosophila that modifies retrotransposon expression and interacts with zeste
-
Mutations in Mosaic suppressor gene (Msu) interact with white alleles induced by insertions of copia, BEL, B104, and mdg3. They also modify transcript abundance of copia. Mutant Msu alleles are recessive lethal. Mutations in this locus are recessive enhancers of zeste, suggesting a connection between the control of retroelement expression and more global pairing-dependent phenomena.
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(1994)
Genetics
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Csink1
Linsk2
Birchler3
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23
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0028303751
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The Doa locus encodes a member of a new protein kinase family and is essential for eye and embryonic development in Drosophila melanogaster
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(1994)
Genes Dev
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Yun1
Farkas2
Lee3
Rabinow4
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25
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0026031940
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Interactions of retrotransposons with the host genome: the case of the gypsy element of Drosophila
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(1991)
Trends Genet
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Corces1
Geyer2
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26
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0024114026
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The Drosophila melanogaster suppressor of Hairy wing protein binds to specific sequences of the gypsy retrotransposon
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(1988)
Genes Dev
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Spana1
Harrison2
Corces3
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28
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0024670895
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Interaction of the Enhancer of white-apricot with transposable element alleles at the white locus in Drosophila melanogaster
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(1989)
Genetics
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Birchler1
Hiebert2
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29
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0024531309
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Interaction of the mottler of white with the transposable element alleles at the white locus in Drosophila melanogasters
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(1989)
Genes Dev
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Birchler1
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31
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0027979821
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Evidence for a role of the Drosophila melanogaster suppressor of sable gene in the pre-mRNA splicing pathway
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Mol Cell Biol
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Fridell1
Searles2
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32
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0025011452
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Copia expression is variable among natural populations of Drosophila
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(1990)
Genetics
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Csink1
McDonald2
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33
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0027930437
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Identification of a strong transcriptional activator for the copia retrotransposon responsible for its differential expression in Drosophila hydei and melanogaster cell lines
-
Identification of a 72 bp regulatory sequence in the 5′ untranslated part of copia that is responsible for the differential expression of 5′ copia: lacZ transgenes in D. hydei versus D. melanogaster cell lines. The differential expression results from the presence of a D. hydei protein that binds to the copia sequence.
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Biochem Biophys Res Commun
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Cavarec1
Jensen2
Heidmann3
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35
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0029127021
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Diverse transposable elements are mobilized in hybrid dysgenesis in Drosophila virilis
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In this paper, we demonstrate a system of hybrid dysgenesis in D. virilis in which at least four unrelated transposable elements are all mobilized following a dysgenic cross. The mobilized elements include a mariner/Tc1 element, a LINE element, a retrotransposon [36], and a DIRS-like element [37].
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(1995)
Proc Natl Acad Sci USA
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Petrov1
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Hartl3
Lozovskaya4
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