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Featured researches published by David A. Wheeler.


Cell | 1984

Molecular analysis of the period locus in Drosophila melanogaster and identification of a transcript involved in biological rhythms

Pranhitha Reddy; William A. Zehring; David A. Wheeler; Vincent Pirrotta; Christopher Hadfield; Jeffrey C. Hall; Michael Rosbash

We have isolated and analyzed DNA sequences encompassing the period (per) locus of Drosophila melanogaster. The location of this clock gene was delimited by the molecular mapping of chromosome aberrations at or very near the per locus. At least five RNAs are transcribed from this region. One of these transcripts, a 0.9 kb species, is strongly implicated in pers control of biological rhythms. Two independently isolated arrhythmic mutations at the per locus dramatically reduce the level of this transcript. Furthermore, the level of the 0.9 kb transcript is strongly modulated during a light/dark cycle. We discuss evidence, from previously reported genetic and phenotypic analysis of pers function, suggesting that this region may be complex and that several gene products from the per region, including this 0.9 kb transcript, may be involved in the different aspects of normal rhythmicity influenced by this clock gene.


Cell | 1984

P-element transformation with period locus DNA restores rhythmicity to mutant, arrhythmic drosophila melanogaster

William A. Zehring; David A. Wheeler; Pranhitha Reddy; Ronald J. Konopka; Charalambos P. Kyriacou; Michael Rosbash; Jeffrey C. Hall

Mutations at the period (per) locus of Drosophila melanogaster disrupt several biological rhythms. Molecular cloning of DNA sequences encompassing the per+ locus has allowed germ-line transformation experiments to be carried out. Certain subsegments of the per region, transduced into the genome of arrhythmic pero flies, restore rhythmicity in circadian locomotor behavior and the males courtship song.


Journal of Neurogenetics | 1986

Germ-Line Transformation Involving DNA from the period Locus in Drosophila melanogaster: Overlapping Genomic Fragments that Restore Circadian and Ultradian Rhythmicity to per0 and per− Mutants

Melanie Hamblen; William A. Zehring; Charalambos P. Kyriacou; Pranhitha Reddy; Qiang Yu; David A. Wheeler; Laurence J. Zwiebel; Ronald J. Konopka; Michael Rosbash; Jeffrey C. Hall

P-element-mediated transformations involving DNA fragments from the period (per) clock gene of Drosophila melanogaster have shown that several subsegments of the locus restore rhythmicity to per0 or per- mutants. Such fragments overlap in a genomic region complementary to one transcript, a 4.5-kb RNA which is probably the per message, in that it is necessary and (in terms of expression from this X-chromosomal locus) sufficient for the flys circadian rhythms. It is also at least necessary for the high-frequency oscillations normally produced by courting males as they vibrate their wings. The entirety of the 4.5-kb transcript is not necessary for rather strong rhythmicity; nor does it seem to be sufficient, in transformants, for wild-type behavioral phenotypes. A 0.9-kb RNA, homologous to genomic region immediately adjacent to the source of the 4.5-kb species, oscillates in its abundance over the course of a day; but coverage of this transcript source in several transformants carrying a per0 mutation--which eliminates the 0.9-kb RNAs oscillation--does not restore rhythmicity. All of the independently isolated arrhythmic mutations tested were covered by the same array of overlapping per+-derived DNA fragments, implying that the only portion of the locus which has mutated to arrhythmicity is complementary to the 4.5-kb transcript.


Behavior Genetics | 1989

Spectral analysis of courtship songs in behavioral mutants of Drosophila melanogaster.

David A. Wheeler; Shankar J. Kulkarni; Donald A. Gailey; Jeffrey C. Hall

Spectral analyses were applied to the courtship songs of the mutantscacophony (cac), dissonance (diss), fruitless (fru), andperiod (per), as well as to the double mutantcac diss. Aberrant intervals between song pulses were observed indiss, cac, cac diss, andfru songs,diss males displayed a defect in song hums manifested by an irregular sine wave, although the fundamental frequencies were normal. Sine song frequencies and intrapulse frequencies were aberrant incac diss males. Two per mutant alleles (pero1 andpers) were associated with normal seng pulses and hums. These findings are discussed with regard to the mechanisms of song production and the role of these sounds inDrosophila reproduction.


Nature Communications | 2015

MLLT1 YEATS domain mutations in clinically distinctive Favourable Histology Wilms tumours.

Elizabeth J. Perlman; Samantha Gadd; Stefan T. Arold; Anand Radhakrishnan; Daniela S. Gerhard; Lawrence J. Jennings; Vicki Huff; Jaime M. Guidry Auvil; Tanja M. Davidsen; Jeffrey S. Dome; Daoud Meerzaman; Chih Hao Hsu; Cu Nguyen; James M. Anderson; Yussanne Ma; Andrew J. Mungall; Richard A. Moore; Marco A. Marra; Charles G. Mullighan; Jing Ma; David A. Wheeler; Oliver A. Hampton; Julie M. Gastier-Foster; Nicole Ross; Malcolm A. Smith

Wilms tumour is an embryonal tumour of childhood that closely resembles the developing kidney. Genomic changes responsible for the development of the majority of Wilms tumours remain largely unknown. Here we identify recurrent mutations within Wilms tumours that involve the highly conserved YEATS domain of MLLT1 (ENL), a gene known to be involved in transcriptional elongation during early development. The mutant MLLT1 protein shows altered binding to acetylated histone tails. Moreover, MLLT1-mutant tumours show an increase in MYC gene expression and HOX dysregulation. Patients with MLLT1-mutant tumours present at a younger age and have a high prevalence of precursor intralobar nephrogenic rests. These data support a model whereby activating MLLT1 mutations early in renal development result in the development of Wilms tumour.


Biological Cybernetics | 1992

Artificial neural network classification of Drosophila courtship song mutants

Eric K. Neumann; David A. Wheeler; Adam S. Bernstein; Jamie W. Burnside; Jeffrey C. Hall

Courtship songs produced by Drosophila males — wild-type, plus the cacophony and dissonance behavioral mutants — were examined with the aid of newly developed strategies for adaptive acoustic analysis and classification. This system used several techniques involving artificial neural networks (a.k.a. parallel distributed processing), including learned vector quantization of signals and non-linear adaption (back-propagation) of data analysis. “Pulse” song from several individual wild-type and mutant males were first vector-quantized according to their frequency spectra. The accumulated quantized data of this kind, for a given song, were then used to “teach” or adapt a multiple-layered feedforward artificial neural network, which classified that song according to its original genotype. Results are presented on the performance of the final adapted system when faced with novel test data and on acoustic features the system decides upon for predicting the song-mutant genotype in question. The potential applications and extensions of this new system are discussed, including how it could be used to screen for courtship mutants, search novel behavior patterns or cause-and-effect relationships associated with reproduction, compress these kinds of data for digital storage, and analyze Drosophila behavior beyond the case of courtship song.


Journal of Biological Rhythms | 1993

Behavior in Light-Dark Cycles of Drosophila Mutants That Are Arrhythmic, Blind, or Both:

David A. Wheeler; Melanie J. Hamblen-Coyle; Mitchell S. Dushay; Jeffrey C. Hall


Journal of Insect Behavior | 1992

Behavior of period-altered circadian rhythm mutants ofDrosophila in light: Dark cycles (Diptera: Drosophilidae)

Melanie J. Hamblen-Coyle; David A. Wheeler; Joan E. Rutila; Michael Rosbash; Jeffrey C. Hall


Behavior Genetics | 1988

Spectral analysis of Drosophila courtship songs: D. melanogaster, D. simulans, and their interspecific hybrid

David A. Wheeler; Warren L. Fields; Jeffrey C. Hall


Archive | 1992

Behavior of period-altered circadian rhythm mutants of Drosophila in light:dark cycles

Melanie J. Hamblen-Coyle; David A. Wheeler; Joan E. Rutila; Michael Rosbash; Janet Hall

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Charles G. Mullighan

St. Jude Children's Research Hospital

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