19 results on '"Hardison, Ross"'
Search Results
2. Defining functional DNA elements in the human genome
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Kellis, Manolis, Wold, Barbara, Snyderd, Michael P., Bernstein, Bradley E., Kundaje, Anshul, Marinov, Georgi K., Ward, Lucas D., Birney, Ewan, Crawford, Gregory E., Dekker, Job, Dunham, Ian, Elnitski, Laura L., Farnham, Peggy J., Feingold, Elise A., Gerstein, Mark, Giddings, Morgan C., Gilbert, David M., Gingeras, Thomas R., Green, Eric D., Guigo, Roderic, Hubbard, Tim, Kent, Jim, Lieb, Jason D., Myerst, Richard M., Pazin, Michael J., Ren, Bing, Stamatoyannopoulos, John A., Weng, Zhiping, White, Kevin P., and Hardison, Ross C.
- Published
- 2014
3. GWAS to Therapy by Genome Edits?
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Hardison, Ross C. and Blobel, Gerd A.
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- 2013
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4. Genome-Wide Organization of GATA1 and TAL1 Determined at High Resolution.
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Han, G. Celine, Vinayachandran, Vinesh, Bataille, Alain R., Bongsoo Park, Ka Yim Chan-Salis, Keller, Cheryl A., Long, Maria, Mahony, Shaun, Hardison, Ross C., and Pugh, B. Franklin
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GENOMES ,GATA proteins ,TAL effectors ,ERYTHROCYTES ,PROGENITOR cells ,CELL differentiation ,GENETIC transcription - Abstract
Erythroid development and differentiation from multiprogenitor cells into red blood cells requires precise transcriptional regulation. Key erythroid transcription factors, GATA1 and TAL1, cooperate, along with other proteins, to regulate many aspects of this process. How GATA1 and TAL1 are juxtaposed along the DNA and their cognate DNA binding site across the mouse genome remains unclear. We applied high-resolution ChIP-exo (chromatin immunoprecipitation followed by 5'-to-3' exonuclease treatment and then massively parallel DNA sequencing) to GATA1 and TAL1 to study their positional organization across the mouse genome during GATA1-dependent maturation. Two complementary methods, MultiGPS and peak pairing, were used to determine high-confidence binding locations by ChIP-exo. We identified ~ 10,000 GATA1 and ~ 15,000 TAL1 locations, which were essentially confirmed by ChIP-seq (chromatin immunoprecipitation followed by massively parallel DNA sequencing). Of these, ~4,000 locations were bound by both GATA1 and TAL1. About three-quarters of them were tightly linked to a partial E-box located 7 or 8 bp upstream of a WGATAA motif. Both TAL1 and GATA1 generated distinct characteristic ChIP-exo peaks around WGATAA motifs that reflect their positional arrangement within a complex. We show that TAL1 and GATA1 form a precisely organized complex at a compound motif consisting of a TG 7 or 8 bp upstream of a WGATAA motif across thousands of genomic locations. [ABSTRACT FROM AUTHOR]
- Published
- 2015
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5. The effects of chromatin organization on variation in mutation rates in the genome.
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Makova, Kateryna D. and Hardison, Ross C.
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CANCER cell growth , *CANCER cell proliferation , *GENOMES , *CHROMATIN , *CANCER invasiveness - Abstract
The variation in local rates of mutations can affect both the evolution of genes and their function in normal and cancer cells. Deciphering the molecular determinants of this variation will be aided by the elucidation of distinct types of mutations, as they differ in regional preferences and in associations with genomic features. Chromatin organization contributes to regional variation in mutation rates, but its contribution differs among mutation types. In both germline and somatic mutations, base substitutions are more abundant in regions of closed chromatin, perhaps reflecting error accumulation late in replication. By contrast, a distinctive mutational state with very high levels of insertions and deletions (indels) and substitutions is enriched in regions of open chromatin. These associations indicate an intricate interplay between the nucleotide sequence of DNA and its dynamic packaging into chromatin, and have important implications for current biomedical research. This Review focuses on recent studies showing associations between chromatin state and mutation rates, including pairwise and multivariate investigations of germline and somatic (particularly cancer) mutations. [ABSTRACT FROM AUTHOR]
- Published
- 2015
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6. Revealing Mammalian Evolutionary Relationships by Comparative Analysis of Gene Clusters.
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Song, Giltae, Riemer, Cathy, Dickins, Benjamin, Kim, Hie Lim, Zhang, Louxin, Zhang, Yu, Hsu, Chih-Hao, Hardison, Ross C., NISC Comparative Sequencing Program, Green, Eric D., and Miller, Webb
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GENOMES ,COMPARATIVE studies ,GENETICS ,GENOTYPES ,GENOME size - Abstract
Many software tools for comparative analysis of genomic sequence data have been released in recent decades. Despite this, it remains challenging to determine evolutionary relationships in gene clusters due to their complex histories involving duplications, deletions, inversions, and conversions. One concept describing these relationships is orthology. Orthologs derive from a common ancestor by speciation, in contrast to paralogs, which derive from duplication. Discriminating orthologs from paralogs is a necessary step in most multispecies sequence analyses, but doing so accurately is impeded by the occurrence of gene conversion events. We propose a refined method of orthology assignment based on two paradigms for interpreting its definition: by genomic context or by sequence content. X-orthology (based on context) traces orthology resulting from speciation and duplication only, while N-orthology (based on content) includes the influence of conversion events. We developed a computational method for automatically mapping both types of orthology on a per-nucleotide basis in gene cluster regions studied by comparative sequencing, and we make this mapping accessible by visualizing the output. All of these steps are incorporated into our newly extended CHAP 2 package. We evaluate our method using both simulated data and real gene clusters (including the well-characterized α-globin and β-globin clusters). We also illustrate use of CHAP 2 by analyzing four more loci: CCL (chemokine ligand), IFN (interferon), CYP2abf (part of cytochrome P450 family 2), and KIR (killer cell immunoglobulin-like receptors). These new methods facilitate and extend our understanding of evolution at these and other loci by adding automated accurate evolutionary inference to the biologist's toolkit. The CHAP 2 package is freely available from http://www.bx.psu.edu/miller_lab. [ABSTRACT FROM PUBLISHER]
- Published
- 2012
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7. Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution.
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Hillier, LaDeana W., Miller, Webb, Birney, Ewan, Warren, Wesley, Hardison, Ross C., Ponting, Chris P., Bork, Peer, Burt, David W., Groenen, Martien A. M., Delany, Mary E., Dodgson, Jerry B., Chinwalla, Asif T., Cliften, Paul F., Clifton, Sandra W., Delehaunty, Kimberly D., Fronick, Catrina, Fulton, Robert S., Graves, Tina A., Kremitzki, Colin, and Layman, Dan
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GENOMES ,POULTRY ,VERTEBRATES ,GENE mapping ,ANIMAL genetics techniques ,CHROMOSOMES - Abstract
We present here a draft genome sequence of the red jungle fowl, Gallus gallus. Because the chicken is a modern descendant of the dinosaurs and the first non-mammalian amniote to have its genome sequenced, the draft sequence of its genome-composed of approximately one billion base pairs of sequence and an estimated 20,000-23,000 genes-provides a new perspective on vertebrate genome evolution, while also improving the annotation of mammalian genomes. For example, the evolutionary distance between chicken and human provides high specificity in detecting functional elements, both non-coding and coding. Notably, many conserved non-coding sequences are far from genes and cannot be assigned to defined functional classes. In coding regions the evolutionary dynamics of protein domains and orthologous groups illustrate processes that distinguish the lineages leading to birds and mammals. The distinctive properties of avian microchromosomes, together with the inferred patterns of conserved synteny, provide additional insights into vertebrate chromosome architecture. [ABSTRACT FROM AUTHOR]
- Published
- 2004
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8. COMPARATIVE GENOMICS.
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Miller, Webb, Makova, Kateryna D., Nekrutenko, Anton, and Hardison, Ross C.
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GENOMES ,MAMMALS ,GENETICS ,BIOINFORMATICS ,COMPUTERS in biology - Abstract
The genomes from three mammals (human, mouse, and rat), two worms, and several yeasts have been sequenced, and more genomes will be completed in the near future for comparison with those of the major model organisms. Scientists have used various methods to align and compare the sequenced genomes to address critical issues in genome function and evolution. This review covers some of the major new insights about gene content, gene regulation, and the fraction of mammalian genomes that are under purifying selection and presumed functional. We review the evolutionary processes that shape genomes, with particular attention to variation in rates within genomes and along different lineages. Internet resources for accessing and analyzing the treasure trove of sequence alignments and annotations are reviewed, and we discuss critical problems to address in new bioinformatic developments in comparative genomics. [ABSTRACT FROM AUTHOR]
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- 2004
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9. Comparative Genomics.
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Hardison, Ross C
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COMPARATIVE genomics , *GENOMES - Abstract
Comparing the genomes of two different species allow the exploration of a host of intriguing evolutionary and genetic questions. [ABSTRACT FROM AUTHOR]
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- 2003
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10. What fraction of the human genome is functional?
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Ponting, Chris P. and Hardison, Ross C.
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NUCLEOTIDES , *GENOMES , *MAMMALS , *HETEROGENEITY , *LABORATORY mice - Abstract
Many evolutionary studies over the past decade have estimated αsel, the proportion of all nucleotides in the human genome that are subject to purifying selection because of their biological function. Most of these studies have estimated the nucleotide substitution rates from genome sequence alignments across many diverse mammals. Some αsel estimates will be affected by the heterogeneity of substitution rates in neutral sequence across the genome. Most will also be inaccurate if change in the functional sequence repertoire occurs rapidly relative to the separation of lineages that are being compared. Evidence gathered from both evolutionary and experimental analyses now indicate that rates of "turnover" of functional, predominantly noncoding, sequence are, indeed, high. They are sufficiently high that an estimated 50% of mouse constrained noncoding sequence is predicted not to be shared with rat, a closely related rodent. The rapidity of turnover results in, at least, a twofold underestimate of αsel by analyses that measure constraint across the eutherian phylogeny. Approaches that take account of turnover estimate that the steady-state value of αsel lies between 10% and 15%. Experimental studies corroborate the predicted rates of loss and gain of noncoding functional sites. These studies show the limitations inherent in the use of deep sequence conservation for identifying functional sequence. Experimental investigations focusing on lineage-specific, noncoding, and functional sequence are now essential if we are to appreciate the complete functional repertoire of the human genome. [ABSTRACT FROM AUTHOR]
- Published
- 2011
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11. Galaxy: A platform for interactive large-scale genome analysis.
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Giardine, Belinda, Riemer, Cathy, Hardison, Ross C., Burhans, Richard, Elnitski, Laura, Prachi Shah, Yi Zhang, Blankenberg, Daniel, Albert, Istvan, Taylor, James, Miller, Webb, Kent, W. James, and Nekrutenko, Anton
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GENOMES , *GENOMICS , *GENETICS , *MEDICINE , *DATABASES - Abstract
Accessing and analyzing the exponentially expanding genomic sequence and functional data pose a challenge for biomedical researchers. Here we describe an interactive system, Galaxy, that combines the power of existing genome annotation databases with a simple Web portal to enable users to search remote resources, combine data from independent queries, and visualize the results. The heart of Galaxy is a flexible history system that stores the queries from each user; performs operations such as intersections, unions, and subtractions; and links to other computational tools. Galaxy can be accessed at http://g2.bx.psu.edu. [ABSTRACT FROM AUTHOR]
- Published
- 2005
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12. ZPicture: Dynamic Alignment and Visualization Tool for Analyzing Conservation Profiles.
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Ovcharenko, Ivan, Loots, Gabriela G., Hardison, Ross C., Miller, Webb, and Stubbs, Lisa
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TRANSCRIPTION factors , *BINDING sites , *NUCLEOTIDE sequence , *GENOMES , *BACTERIA , *GENETIC code - Abstract
Describes the use of comparative sequence analysis in identifying functional coding and noncoding elements conserved throughout evolution in the U.S. Presence of conserved transcription factor-binding sites; Adjustment of the threshold levels of conservation; Alignment of the microbial genomes.
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- 2004
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13. 28-Way vertebrate alignment and conservation track in the UCSC Genome Browser.
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Miller, Webb, Rosenbloom, Kate, Hardison, Ross C., Minmei Hou, Taylor, James, Raney, Brian, Burhans, Richard, King, David C., Baertsch, Robert, Blankenberg, Daniel, Kosakovsky Pond, Sergei L., Nekrutenko, Anton, Giardine, Belinda, Harris, Robert S., Tyekucheva, Svitlana, Diekhans, Mark, Pringle, Thomas H., Murphy, William J., Lesk, Arthur, and Weinstock, George M.
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VERTEBRATES , *GENOMES , *NUCLEOTIDE sequence , *HUMAN genome , *MAMMAL genetics - Abstract
This article describes a set of alignments of 28 vertebrate genome sequences that is provided by the UCSC Genome Browser. The alignments can be viewed on the Human Genome Browser (March 2006 assembly) at http://genome.ucsc.edu, downloaded in bulk by anonymous FTP from http://hgdownload.cse.ucsc.edu/goldenPath/hg18/multiz28way, or analyzed with the Galaxy server at http://g2.bx.psu.edu. This article illustrates the power of this resource for exploring vertebrate and mammalian evolution, using three examples. First, we present several vignettes involving insertions and deletions within protein-coding regions, including a look at some human-specific indels. Then we study the extent to which start codons and stop codons in the human sequence are conserved in other species, showing that start codons are in general more poorly conserved than stop codons. Finally, an investigation of the phylogenetic depth of conservation for several classes of functional elements in the human genome reveals striking differences in the rates and modes of decay in alignability. Each functional class has a distinctive period of stringent constraint, followed by decays that allow (for the case of regulatory regions) or reject (for coding regions and ultraconserved elements) insertions and deletions. [ABSTRACT FROM AUTHOR]
- Published
- 2007
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14. Evaluation of regulatory potential and conservation scores for detecting cis-regulatory modules in aligned mammalian genome sequences.
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King, David C., Taylor, James, Elnitski, Laura, Chiaromonte, Francesca, Miller, Webb, and Hardison, Ross C.
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GENOMES , *MAMMALS , *NUCLEOTIDE sequence , *GENES , *GENOMICS , *BIOINFORMATICS - Abstract
Techniques of comparative genomics are being used to identify candidate functional DNA sequences, and objective evaluations are needed to assess their effectiveness. Different analytical methods score distinctive features of whole-genome alignments among human, mouse, and rat to predict functional regions. We evaluated three of these methods for their ability to identify the positions of known regulatory regions in the well-studied HBB gene complex. Two methods, multispecies conserved sequences and phastCons, quantify levels of conservation to estimate a likelihood that aligned DNA sequences are under purifying selection. A third function, regulatory potential (RP), measures the similarity of patterns in the alignments to those in known regulatory regions. The methods can correctly identify 50%–60% of noncoding positions in the HBB gene complex as regulatory or nonregulatory, with RP performing better than do other methods. When evaluated by the ability to discriminate genomic intervals, RP reaches a sensitivity of 0.78 and a true discovery rate of ∼0.6. The performance is better on other reference sets; both phastCons and RP scores can capture almost all regulatory elements in those sets along with ∼7% of the human genome. [ABSTRACT FROM AUTHOR]
- Published
- 2005
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15. Mulan: Multiple-sequence local alignment and visualization for studying function and evolution.
- Author
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Ovcharenko, Ivan, Loots, Gabriela C., Giardine, Belinda M., Minmei Hou, Jian Ma, Hardison, Ross C., Stubbs, Lisa, and Miller, Webb
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GENOMES , *PHYLOGENY , *GENES , *VERTEBRATES , *INTRONS , *GENETIC transcription - Abstract
Multiple-sequence alignment analysis is a powerful approach for understanding phylogenetic relationships, annotating genes, and detecting functional regulatory elements. With a growing number of partly or fully sequenced vertebrate genomes, effective tools for performing multiple comparisons are required to accurately and efficiently assist biological discoveries. Here we introduce Mulan (http://mulan.dcode.org/), a novel method and a network server for comparing multiple draft and finished-quality sequences to identify functional elements conserved over evolutionary time. Mulan brings together several novel algorithms: the TBA multi-aligner program for rapid identification of local sequence conservation, and the multiTF program for detecting evolutionarily conserved transcription factor binding sites in multiple alignments. In addition, Mulan supports two-way communication with the GALA database; alignments of multiple spedes dynamically generated in GALA can be viewed in Mulan, and conserved transcription factor binding sites identified with Mulan / multiTF can be integrated and overlaid with extensive genome annotation data using GALA. Local multiple alignments computed by Mulan ensure reliable representation of short- and large-scale genomic rearrangements in distant organisms. Mulan allows for interactive modification of critical conservation parameters to differentially predict conserved regions in comparisons of both closely and distantly related species. We illustrate the uses and applications of the Mulan tool through multispecies comparisons of the GATA3 gene locus and the identification of elements that are conserved in a different way in avians than in other genomes, allowing speculation on the evolution of birds. Source code for the aligners and the aligner-evaluation software can be freely downloaded from http://www.bx.psu.edu/miller_lab/. [ABSTRACT FROM AUTHOR]
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- 2005
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16. Regulatory Potential Scores From Genome-Wide Three-Way Alignments of Human, Mouse, and Rat.
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Kolbe, Diana, Taylor, James, Elnitski, Laura, Eswara, Pallavi, Jia Li, Miller, Webb, Hardison, Ross, and Chiaromonte, Francesca
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GENOMES , *HUMAN beings , *RATS , *MICE , *NUCLEOTIDE sequence , *GENOMICS - Abstract
We generalize the computation of the Regulatory Potential (RP) score from two-way alignments of human and mouse to three-way alignments of human, mouse, and rat. This requires overcoming technical challenges that arise because the complexity of the models underlying the score increases exponentially with the number of species. Despite the close evolutionary proximity of rat to mouse, we find that adding the rat sequence increases our ability to predict genomic sites that regulate gene transcription. A variant of the RP scoring scheme that accounts for local variation in neutral mutational patterns further improves our predictions. [ABSTRACT FROM AUTHOR]
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- 2004
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17. Patterns of Insertions and Their Covariation With Substititions in the Rat, Mouse, and Human Genomes.
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Shan Yang, Smit, Arian F., Schwartz, Scott, Chiaromonte, Francesca, Roskin, Krishna M., Haussler, David, Miller, Webb, and Hardison, Ross C.
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GENOMES , *RATS , *HUMAN genome , *DNA , *GENETICS , *RODENTS - Abstract
The rates at which human genomic DNA changes by neutral substitution and insertion of certain families of transposable elements covary in large, megabase-sized segments. We used the rat, mouse, and human genomic DNA sequences to examine these processes in more detail in comparisons over both shorter (rat-mouse) and longer (rodent-primate) times, and demonstrated the generality of the covariation. Different families of transposable elements show distinctive insertion preferences and patterns of variation with substitution rates. SINEs are more abundant in GC-rich DNA, but the regional GC preference for insertion (monitored in young SINEs) differs between rodents and humans. In contrast, insertions in the rodent genomes are predominantly LINEs, which prefer to insert into AT-rich DNA in all three mammals. The insertion frequency of repeats other than SINEs correlates strongly positively with the frequency of substitutions in all species. However, correlations with SINEs show the opposite effects. The correlations are explained only in part by the GC content, indicating that other factors also contribute to the inherent tendency of DNA segments to change over evolutionary time. [ABSTRACT FROM AUTHOR]
- Published
- 2004
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18. ESPERR: Learning strong and weak signals in genomic sequence alignments to identify functional elements.
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Taylor, James, Tyekucheva, Svitlana, King, David C., Hardison, Ross C., Miller, Webb, and Chiaromonte, Francesca
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COMPUTATIONAL biology , *GENOMICS , *GENOMES , *GENETICS , *GENES - Abstract
Genomic sequence signals--such as base composition, presence of particular motifs, or evolutionary constraint--have been used effectively to identify functional elements. However, approaches based only on specific signals known to correlate with function can be quite limiting. When training data are available, application of computational learning algorithms to multispecies alignments has the potential to capture broader and more informative sequence and evolutionary patterns that better characterize a class of elements. However, effective exploitation of patterns in multispecies alignments is impeded by the vast number of possible alignment columns and by a limited understanding of which particular strings of columns may characterize a given class. We have developed a computational method, called ESPERR (evolutionary and sequence pattern extraction through reduced representations), which uses training examples to learn encodings of multispecies alignments into reduced forms tailored for the prediction of chosen classes of functional elements. ESPERR produces a greatly improved Regulatory Potential score, which can discriminate regulatory regions from neutral sites with excellent accuracy (∼ 94%). This score captures strong signals (GC content and conservation), as well as subtler signals (with small contributions from many different alignment patterns) that characterize the regulatory elements in our training set. ESPERR is also effective for predicting other classes of functional elements, as we show for DNaseI hypersensitive sites and highly conserved regions with developmental enhancer activity. Our software, training data, and genome-wide predictions are available from our Web site (http://www.bx.psu.edu/projects/esperr). [ABSTRACT FROM AUTHOR]
- Published
- 2006
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19. Experimental validation of predicted mammalian erythroid cis-regulatory modules.
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Hao Wang, Ying Zhang, Yong Cheng, Yuepin Zhou, King, David C., Taylor, James, Chiaromonte, Francesca, Kasturi, Jyotsna, Petrykowska, Hanna, Gibb, Brian, Dorman, Christine, Miller, Webb, Dore, Louis C., Welch, John, Weiss, Mitchell J., and Hardison, Ross C.
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ERYTHROCYTES , *GENOMICS , *GENOMES , *GENETICS , *GENES , *TRANSCRIPTION factors - Abstract
Multiple alignments of genome sequences are helpful guides to functional analysis, but predicting cis-regulatory modules (CRMs) accurately from such alignments remains an elusive goal. We predict CRMs for mammalian genes expressed in red blood cells by combining two properties gleaned from aligned, noncoding genome sequences: a positive regulatory potential (RP) score, which detects similarity to patterns in alignments distinctive for regulatory regions, and conservation of a binding site motif for the essential erythroid transcription factor GATA-1. Within eight target loci, we tested 75 noncoding segments by reporter gene assays in transiently transfected human K562 cells and/or after site-directed integration into murine erythroleukemia cells. Segments with a high RP score and a conserved exact match to the binding site consensus are validated at a good rate (50%-100%, with rates increasing at higher RP), whereas segments with lower RP scores or nonconsensus binding motifs tend to be inactive. Active DNA segments were shown to be occupied by GATA-1 protein by chromatin immunoprecipitation, whereas sites predicted to be inactive were not occupied. We verify four previously known erythroid CRMs and identify 28 novel ones. Thus, high RP in combination with another feature of a CRM, such as a conserved transcription factor binding site, is a good predictor of functional CRMs. Genome-wide predictions based on RP and a large set of well-defined transcription factor binding sites are available through servers at http://www.bx.psu.edu/. [ABSTRACT FROM AUTHOR]
- Published
- 2006
- Full Text
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