Amy Beaton
University of California, Berkeley
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Featured researches published by Amy Beaton.
Genome Biology | 2002
Pavel Tomancak; Amy Beaton; Richard Weiszmann; Elaine Kwan; ShengQiang Shu; Suzanna E. Lewis; Stephen Richards; Michael Ashburner; Volker Hartenstein; Susan E. Celniker; Gerald M. Rubin
BackgroundCell-fate specification and tissue differentiation during development are largely achieved by the regulation of gene transcription.ResultsAs a first step to creating a comprehensive atlas of gene-expression patterns during Drosophila embryogenesis, we examined 2,179 genes by in situ hybridization to fixed Drosophila embryos. Of the genes assayed, 63.7% displayed dynamic expression patterns that were documented with 25,690 digital photomicrographs of individual embryos. The photomicrographs were annotated using controlled vocabularies for anatomical structures that are organized into a developmental hierarchy. We also generated a detailed time course of gene expression during embryogenesis using microarrays to provide an independent corroboration of the in situ hybridization results. All image, annotation and microarray data are stored in publicly available database. We found that the RNA transcripts of about 1% of genes show clear subcellular localization. Nearly all the annotated expression patterns are distinct. We present an approach for organizing the data by hierarchical clustering of annotation terms that allows us to group tissues that express similar sets of genes as well as genes displaying similar expression patterns.ConclusionsAnalyzing gene-expression patterns by in situ hybridization to whole-mount embryos provides an extremely rich dataset that can be used to identify genes involved in developmental processes that have been missed by traditional genetic analysis. Systematic analysis of rigorously annotated patterns of gene expression will complement and extend the types of analyses carried out using expression microarrays.
Genome Biology | 2007
Pavel Tomancak; Benjamin P. Berman; Amy Beaton; Richard Weiszmann; Elaine Kwan; Volker Hartenstein; Susan E. Celniker; Gerald M. Rubin
BackgroundCell and tissue specific gene expression is a defining feature of embryonic development in multi-cellular organisms. However, the range of gene expression patterns, the extent of the correlation of expression with function, and the classes of genes whose spatial expression are tightly regulated have been unclear due to the lack of an unbiased, genome-wide survey of gene expression patterns.ResultsWe determined and documented embryonic expression patterns for 6,003 (44%) of the 13,659 protein-coding genes identified in the Drosophila melanogaster genome with over 70,000 images and controlled vocabulary annotations. Individual expression patterns are extraordinarily diverse, but by supplementing qualitative in situ hybridization data with quantitative microarray time-course data using a hybrid clustering strategy, we identify groups of genes with similar expression. Of 4,496 genes with detectable expression in the embryo, 2,549 (57%) fall into 10 clusters representing broad expression patterns. The remaining 1,947 (43%) genes fall into 29 clusters representing restricted expression, 20% patterned as early as blastoderm, with the majority restricted to differentiated cell types, such as epithelia, nervous system, or muscle. We investigate the relationship between expression clusters and known molecular and cellular-physiological functions.ConclusionNearly 60% of the genes with detectable expression exhibit broad patterns reflecting quantitative rather than qualitative differences between tissues. The other 40% show tissue-restricted expression; the expression patterns of over 1,500 of these genes are documented here for the first time. Within each of these categories, we identified clusters of genes associated with particular cellular and developmental functions.
Genetics | 1999
Allan C. Spradling; David B. Stern; Amy Beaton; E J Rhem; Todd R. Laverty; N. Mozden; Sima Misra; Gerald M. Rubin
Genetics | 1988
Istvan Kiss; Amy Beaton; Jil C. Tardiff; Dianne Fristrom; James W. Fristrom
Genetics | 1988
Amy Beaton; I. Kiss; Dianne Fristrom; James W. Fristrom
PLOS Biology | 2008
Xiao-Yong Li; Stewart MacArthur; Richard Bourgon; David A. Nix; Daniel A. Pollard; Venky N. Iyer; Aaron Hechmer; Lisa Simirenko; Mark Stapleton; Cris L. Luengo Hendriks; Hou Cheng Chu; Nobuo Ogawa; William Inwood; Victor Sementchenko; Amy Beaton; Richard Weiszmann; Susan E. Celniker; David W. Knowles; Thomas R. Gingeras; Terence P. Speed; Michael B. Eisen; Mark D. Biggin
Archive | 2011
Pavel Tomancak; Amy Beaton; Richard Weiszmann; Elaine Kwan; ShengQiang Shu; Suzanna E. Lewis; Stephen Richards; Michael Ashburner; Volker Hartenstein; Susan E Celniker; Gerald M. Rubin
Lawrence Berkeley National Laboratory | 2008
Xiao-Yong Li; Stewart MacArthur; Richard Bourgon; David A. Nix; Daniel A. Pollard; Venky N. Iyer; Aaron Hechmer; Lisa Simirenko; Mark Stapleton; Cris L. Luengo Hendriks; Hou Cheng Chu; Nobuo Ogawa; William Inwood; Victor Sementchenko; Amy Beaton; Richard Weiszmann; Susan E. Celniker; David W. Knowles; Thomas R. Gingeras; Terence P. Speed; Michael B. Eisen; Mark D. Biggin
Archive | 2007
Soile V.E. Keranen; Cristian L. Luengo Hendriks; Charless C. Fowlkes; Lisa Simirenko; Gunther H. Weber; Oliver Ruebel; Min-Yu Huang; Angela H. DePace; Clara Henriquez; Xiao-Yong Li; Hou C. Chu; David W. Kaszuba; Amy Beaton; Susan E Celniker; Bernd Hamann; Michael B. Eisen; Jitendra Malik; David W. Knowles; Mark D. Biggin
Genetics | 1999
Allan C. Spradling; David B. Stern; Amy Beaton; Rehm Ej; Todd R. Laverty; N. Mozden; Sima Misra; Gerald M. Rubin