Genomic localization of RNA binding proteins reveals links between pre-mRNA processing and transcription.

Abstract:

:Pre-mRNA processing often occurs in coordination with transcription thereby coupling these two key regulatory events. As such, many proteins involved in mRNA processing associate with the transcriptional machinery and are in proximity to DNA. This proximity allows for the mapping of the genomic associations of RNA binding proteins by chromatin immunoprecipitation (ChIP) as a way of determining their sites of action on the encoded mRNA. Here, we used ChIP combined with high-density microarrays to localize on the human genome three functionally distinct RNA binding proteins: the splicing factor polypyrimidine tract binding protein (PTBP1/hnRNP I), the mRNA export factor THO complex subunit 4 (ALY/THOC4), and the 3' end cleavage stimulation factor 64 kDa (CSTF2). We observed interactions at promoters, internal exons, and 3' ends of active genes. PTBP1 had biases toward promoters and often coincided with RNA polymerase II (RNA Pol II). The 3' processing factor, CSTF2, had biases toward 3' ends but was also observed at promoters. The mRNA processing and export factor, ALY, mapped to some exons but predominantly localized to introns and did not coincide with RNA Pol II. Because the RNA binding proteins did not consistently coincide with RNA Pol II, the data support a processing mechanism driven by reorganization of transcription complexes as opposed to a scanning mechanism. In sum, we present the mapping in mammalian cells of RNA binding proteins across a portion of the genome that provides insight into the transcriptional assembly of RNA-protein complexes.

journal_name

Genome Res

journal_title

Genome research

authors

Swinburne IA,Meyer CA,Liu XS,Silver PA,Brodsky AS

doi

10.1101/gr.5211806

subject

Has Abstract

pub_date

2006-07-01 00:00:00

pages

912-21

issue

7

eissn

1088-9051

issn

1549-5469

pii

gr.5211806

journal_volume

16

pub_type

杂志文章
  • Cell-type, allelic, and genetic signatures in the human pancreatic beta cell transcriptome.

    abstract::Elucidating the pathophysiology and molecular attributes of common disorders as well as developing targeted and effective treatments hinges on the study of the relevant cell type and tissues. Pancreatic beta cells within the islets of Langerhans are centrally involved in the pathogenesis of both type 1 and type 2 diab...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.150706.112

    authors: Nica AC,Ongen H,Irminger JC,Bosco D,Berney T,Antonarakis SE,Halban PA,Dermitzakis ET

    更新日期:2013-09-01 00:00:00

  • Shuffling of genes within low-copy repeats on 22q11 (LCR22) by Alu-mediated recombination events during evolution.

    abstract::Low-copy repeats, or segmental duplications, are highly dynamic regions in the genome. The low-copy repeats on chromosome 22q11.2 (LCR22) are a complex mosaic of genes and pseudogenes formed by duplication processes; they mediate chromosome rearrangements associated with velo-cardio-facial syndrome/DiGeorge syndrome, ...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.1549503

    authors: Babcock M,Pavlicek A,Spiteri E,Kashork CD,Ioshikhes I,Shaffer LG,Jurka J,Morrow BE

    更新日期:2003-12-01 00:00:00

  • Transcription factor binding and modified histones in human bidirectional promoters.

    abstract::Bidirectional promoters have received considerable attention because of their ability to regulate two downstream genes (divergent genes). They are also highly abundant, directing the transcription of approximately 11% of genes in the human genome. We categorized the presence of DNA sequence motifs, binding of transcri...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.5623407

    authors: Lin JM,Collins PJ,Trinklein ND,Fu Y,Xi H,Myers RM,Weng Z

    更新日期:2007-06-01 00:00:00

  • Genetic and phenotypic intra-species variation in Candida albicans.

    abstract::Candida albicans is a commensal fungus of the human gastrointestinal tract and a prevalent opportunistic pathogen. To examine diversity within this species, extensive genomic and phenotypic analyses were performed on 21 clinical C. albicans isolates. Genomic variation was evident in the form of polymorphisms, copy num...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.174623.114

    authors: Hirakawa MP,Martinez DA,Sakthikumar S,Anderson MZ,Berlin A,Gujja S,Zeng Q,Zisson E,Wang JM,Greenberg JM,Berman J,Bennett RJ,Cuomo CA

    更新日期:2015-03-01 00:00:00

  • Conservation of regulatory sequences and gene expression patterns in the disintegrating Drosophila Hox gene complex.

    abstract::Homeotic (Hox) genes are usually clustered and arranged in the same order as they are expressed along the anteroposterior body axis of metazoans. The mechanistic explanation for this colinearity has been elusive, and it may well be that a single and universal cause does not exist. The Hox-gene complex (HOM-C) has been...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.3468605

    authors: Negre B,Casillas S,Suzanne M,Sánchez-Herrero E,Akam M,Nefedov M,Barbadilla A,de Jong P,Ruiz A

    更新日期:2005-05-01 00:00:00

  • Analysis of the floral transcriptome uncovers new regulators of organ determination and gene families related to flower organ differentiation in Gerbera hybrida (Asteraceae).

    abstract::Development of composite inflorescences in the plant family Asteraceae has features that cannot be studied in the traditional model plants for flower development. In Gerbera hybrida, inflorescences are composed of morphologically different types of flowers tightly packed into a flower head (capitulum). Individual flor...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.3043705

    authors: Laitinen RA,Immanen J,Auvinen P,Rudd S,Alatalo E,Paulin L,Ainasoja M,Kotilainen M,Koskela S,Teeri TH,Elomaa P

    更新日期:2005-04-01 00:00:00

  • A novel k-mer set memory (KSM) motif representation improves regulatory variant prediction.

    abstract::The representation and discovery of transcription factor (TF) sequence binding specificities is critical for understanding gene regulatory networks and interpreting the impact of disease-associated noncoding genetic variants. We present a novel TF binding motif representation, the k-mer set memory (KSM), which consist...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.226852.117

    authors: Guo Y,Tian K,Zeng H,Guo X,Gifford DK

    更新日期:2018-06-01 00:00:00

  • Yeast genetic interaction screen of human genes associated with amyotrophic lateral sclerosis: identification of MAP2K5 kinase as a potential drug target.

    abstract::To understand disease mechanisms, a large-scale analysis of human-yeast genetic interactions was performed. Of 1305 human disease genes assayed, 20 genes exhibited strong toxicity in yeast. Human-yeast genetic interactions were identified by en masse transformation of the human disease genes into a pool of 4653 homozy...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.211649.116

    authors: Jo M,Chung AY,Yachie N,Seo M,Jeon H,Nam Y,Seo Y,Kim E,Zhong Q,Vidal M,Park HC,Roth FP,Suk K

    更新日期:2017-09-01 00:00:00

  • Sister chromatid telomere fusions, but not NHEJ-mediated inter-chromosomal telomere fusions, occur independently of DNA ligases 3 and 4.

    abstract::Telomeres shorten with each cell division and can ultimately become substrates for nonhomologous end-joining repair, leading to large-scale genomic rearrangements of the kind frequently observed in human cancers. We have characterized more than 1400 telomere fusion events at the single-molecule level, using a combinat...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.200840.115

    authors: Liddiard K,Ruis B,Takasugi T,Harvey A,Ashelford KE,Hendrickson EA,Baird DM

    更新日期:2016-05-01 00:00:00

  • Nonrandom domain organization of the Arabidopsis genome at the nuclear periphery.

    abstract::The nuclear space is not a homogeneous biochemical environment. Many studies have demonstrated that the transcriptional activity of a gene is linked to its positioning within the nuclear space. Following the discovery of lamin-associated domains (LADs), which are transcriptionally repressed chromatin regions, the nonr...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.215186.116

    authors: Bi X,Cheng YJ,Hu B,Ma X,Wu R,Wang JW,Liu C

    更新日期:2017-07-01 00:00:00

  • Multiple waves of recent DNA transposon activity in the bat, Myotis lucifugus.

    abstract::DNA transposons, or class 2 transposable elements, have successfully propagated in a wide variety of genomes. However, it is widely believed that DNA transposon activity has ceased in mammalian genomes for at least the last 40 million years. We recently reported evidence for the relatively recent activity of hAT and H...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.071886.107

    authors: Ray DA,Feschotte C,Pagan HJ,Smith JD,Pritham EJ,Arensburger P,Atkinson PW,Craig NL

    更新日期:2008-05-01 00:00:00

  • Introgression maintains the genetic integrity of the mating-type determining chromosome of the fungus Neurospora tetrasperma.

    abstract::Genome evolution is driven by a complex interplay of factors, including selection, recombination, and introgression. The regions determining sexual identity are particularly dynamic parts of eukaryotic genomes that are prone to molecular degeneration associated with suppressed recombination. In the fungus Neurospora t...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.197244.115

    authors: Corcoran P,Anderson JL,Jacobson DJ,Sun Y,Ni P,Lascoux M,Johannesson H

    更新日期:2016-04-01 00:00:00

  • Detecting genetic variation in microarray expression data.

    abstract::The use of high-density oligonucleotide arrays to measure the expression levels of thousands of genes in parallel has become commonplace. To take further advantage of the growing body of data, we developed a method, termed "GeSNP," to mine the detailed hybridization patterns in oligonucleotide array expression data fo...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.6307307

    authors: Greenhall JA,Zapala MA,Cáceres M,Libiger O,Barlow C,Schork NJ,Lockhart DJ

    更新日期:2007-08-01 00:00:00

  • Probing genomic diversity and evolution of Escherichia coli O157 by single nucleotide polymorphisms.

    abstract::Infections by Shiga toxin-producing Escherichia coli O157:H7 (STEC O157) are the predominant cause of bloody diarrhea and hemolytic uremic syndrome in the United States. In silico comparison of the two complete STEC O157 genomes (Sakai and EDL933) revealed a strikingly high level of sequence identity in orthologous pr...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.4759706

    authors: Zhang W,Qi W,Albert TJ,Motiwala AS,Alland D,Hyytia-Trees EK,Ribot EM,Fields PI,Whittam TS,Swaminathan B

    更新日期:2006-06-01 00:00:00

  • Copy number variation at the breakpoint region of isochromosome 17q.

    abstract::Isochromosome 17q, or i(17q), is one of the most frequent nonrandom changes occurring in human neoplasia. Most of the i(17q) breakpoints cluster within a approximately 240-kb interval located in the Smith-Magenis syndrome common deletion region in 17p11.2. The breakpoint cluster region is characterized by a complex ar...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.080697.108

    authors: Carvalho CM,Lupski JR

    更新日期:2008-11-01 00:00:00

  • Genome-wide mapping of human DNA-replication origins: levels of transcription at ORC1 sites regulate origin selection and replication timing.

    abstract::We report the genome-wide mapping of ORC1 binding sites in mammals, by chromatin immunoprecipitation and parallel sequencing (ChIP-seq). ORC1 binding sites in HeLa cells were validated as active DNA replication origins (ORIs) using Repli-seq, a method that allows identification of ORI-containing regions by parallel se...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.142331.112

    authors: Dellino GI,Cittaro D,Piccioni R,Luzi L,Banfi S,Segalla S,Cesaroni M,Mendoza-Maldonado R,Giacca M,Pelicci PG

    更新日期:2013-01-01 00:00:00

  • Retroelement distributions in the human genome: variations associated with age and proximity to genes.

    abstract::Remnants of more than 3 million transposable elements, primarily retroelements, comprise nearly half of the human genome and have generated much speculation concerning their evolutionary significance. We have exploited the draft human genome sequence to examine the distributions of retroelements on a genome-wide scale...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.388902

    authors: Medstrand P,van de Lagemaat LN,Mager DL

    更新日期:2002-10-01 00:00:00

  • Evolutionary constraints in conserved nongenic sequences of mammals.

    abstract::Mammalian genomes contain many highly conserved nongenic sequences (CNGs) whose functional significance is poorly understood. Sets of CNGs have previously been identified by selecting the most conserved elements from a chromosome or genome, but in these highly selected samples, conservation may be unrelated to purifyi...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.3942005

    authors: Keightley PD,Kryukov GV,Sunyaev S,Halligan DL,Gaffney DJ

    更新日期:2005-10-01 00:00:00

  • Characterizing the genetic basis of transcriptome diversity through RNA-sequencing of 922 individuals.

    abstract::Understanding the consequences of regulatory variation in the human genome remains a major challenge, with important implications for understanding gene regulation and interpreting the many disease-risk variants that fall outside of protein-coding regions. Here, we provide a direct window into the regulatory consequen...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.155192.113

    authors: Battle A,Mostafavi S,Zhu X,Potash JB,Weissman MM,McCormick C,Haudenschild CD,Beckman KB,Shi J,Mei R,Urban AE,Montgomery SB,Levinson DF,Koller D

    更新日期:2014-01-01 00:00:00

  • Multiparameter functional diversity of human C2H2 zinc finger proteins.

    abstract::C2H2 zinc finger proteins represent the largest and most enigmatic class of human transcription factors. Their C2H2-ZF arrays are highly variable, indicating that most will have unique DNA binding motifs. However, most of the binding motifs have not been directly determined. In addition, little is known about whether ...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.209643.116

    authors: Schmitges FW,Radovani E,Najafabadi HS,Barazandeh M,Campitelli LF,Yin Y,Jolma A,Zhong G,Guo H,Kanagalingam T,Dai WF,Taipale J,Emili A,Greenblatt JF,Hughes TR

    更新日期:2016-12-01 00:00:00

  • Comparative gene mapping: a fine-scale survey of chromosome rearrangements between ruminants and humans.

    abstract::A total of 202 genes were cytogenetically mapped to goat chromosomes, multiplying by five the total number of regional gene localizations in domestic ruminants (255). This map encompasses 249 and 173 common anchor loci regularly spaced along human and murine chromosomes, respectively, which makes it possible to perfor...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.8.9.901

    authors: Schibler L,Vaiman D,Oustry A,Giraud-Delville C,Cribiu EP

    更新日期:1998-09-01 00:00:00

  • Integrative functional genomics identifies an enhancer looping to the SOX9 gene disrupted by the 17q24.3 prostate cancer risk locus.

    abstract::Genome-wide association studies (GWAS) are identifying genetic predisposition to various diseases. The 17q24.3 locus harbors the single nucleotide polymorphism (SNP) rs1859962 that is statistically associated with prostate cancer (PCa). It defines a 130-kb linkage disequilibrium (LD) block that lies in an ∼2-Mb gene d...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.135665.111

    authors: Zhang X,Cowper-Sal lari R,Bailey SD,Moore JH,Lupien M

    更新日期:2012-08-01 00:00:00

  • Nucleosome occupancy as a novel chromatin parameter for replication origin functions.

    abstract::Eukaryotic DNA replication initiates from multiple discrete sites in the genome, termed origins of replication (origins). Prior to S phase, multiple origins are poised to initiate replication by recruitment of the pre-replicative complex (pre-RC). For proper replication to occur, origin activation must be tightly regu...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.209940.116

    authors: Rodriguez J,Lee L,Lynch B,Tsukiyama T

    更新日期:2017-02-01 00:00:00

  • The human obese (OB) gene: RNA expression pattern and mapping on the physical, cytogenetic, and genetic maps of chromosome 7.

    abstract::The recently identified mouse obese (ob) gene apparently encodes a secreted protein that may function in the signaling pathway of adipose tissue. Mutations in the mouse ob gene are associated with the early development of gross obesity. A detailed knowledge concerning the RNA expression pattern and precise genomic loc...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.5.1.5

    authors: Green ED,Maffei M,Braden VV,Proenca R,DeSilva U,Zhang Y,Chua SC Jr,Leibel RL,Weissenbach J,Friedman JM

    更新日期:1995-08-01 00:00:00

  • Methylation analysis of a marsupial X-linked CpG island by bisulfite genomic sequencing.

    abstract::Paternal X chromosome inactivation occurs in rodent extraembryonic membranes and in all tissues of marsupials. Methylation of CpG islands occurs on the inactive X in eutherians and is considered to be a stabilizing mechanism. The only previous study of a marsupial X-linked CpG island was of the G6PD gene of the Virgin...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.6.2.114

    authors: Loebel DA,Johnston PG

    更新日期:1996-02-01 00:00:00

  • Distribution of hammerhead and hammerhead-like RNA motifs through the GenBank.

    abstract::Hammerhead ribozymes previously were found in satellite RNAs from plant viroids and in repetitive DNA from certain species of newts and schistosomes. To determine if this catalytic RNA motif has a wider distribution, we decided to scrutinize the GenBank database for RNAs that contain hammerhead or hammerhead-like moti...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.10.7.1011

    authors: Ferbeyre G,Bourdeau V,Pageau M,Miramontes P,Cedergren R

    更新日期:2000-07-01 00:00:00

  • Principled multi-omic analysis reveals gene regulatory mechanisms of phenotype variation.

    abstract::Recent studies have analyzed large-scale data sets of gene expression to identify genes associated with interindividual variation in phenotypes ranging from cancer subtypes to drug sensitivity, promising new avenues of research in personalized medicine. However, gene expression data alone is limited in its ability to ...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.227066.117

    authors: Hanson C,Cairns J,Wang L,Sinha S

    更新日期:2018-08-01 00:00:00

  • Gene regulation and speciation in house mice.

    abstract::One approach to understanding the process of speciation is to characterize the genetic architecture of post-zygotic isolation. As gene regulation requires interactions between loci, negative epistatic interactions between divergent regulatory elements might underlie hybrid incompatibilities and contribute to reproduct...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.195743.115

    authors: Mack KL,Campbell P,Nachman MW

    更新日期:2016-04-01 00:00:00

  • Assessing clusters and motifs from gene expression data.

    abstract::Large-scale gene expression studies and genomic sequencing projects are providing vast amounts of information that can be used to identify or predict cellular regulatory processes. Genes can be clustered on the basis of the similarity of their expression profiles or function and these clusters are likely to contain ge...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.148301

    authors: Jakt LM,Cao L,Cheah KS,Smith DK

    更新日期:2001-01-01 00:00:00

  • High resolution mapping of modified DNA nucleobases using excision repair enzymes.

    abstract::The incorporation and creation of modified nucleobases in DNA have profound effects on genome function. We describe methods for mapping positions and local content of modified DNA nucleobases in genomic DNA. We combined in vitro nucleobase excision with massively parallel DNA sequencing (Excision-seq) to determine the...

    journal_title:Genome research

    pub_type: 杂志文章

    doi:10.1101/gr.174052.114

    authors: Bryan DS,Ransom M,Adane B,York K,Hesselberth JR

    更新日期:2014-09-01 00:00:00