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1.
Nat Genet ; 39(10): 1217-24, 2007 Oct.
Article in English | MEDLINE | ID: mdl-17873874

ABSTRACT

Genetic variation influences gene expression, and this variation in gene expression can be efficiently mapped to specific genomic regions and variants. Here we have used gene expression profiling of Epstein-Barr virus-transformed lymphoblastoid cell lines of all 270 individuals genotyped in the HapMap Consortium to elucidate the detailed features of genetic variation underlying gene expression variation. We find that gene expression is heritable and that differentiation between populations is in agreement with earlier small-scale studies. A detailed association analysis of over 2.2 million common SNPs per population (5% frequency in HapMap) with gene expression identified at least 1,348 genes with association signals in cis and at least 180 in trans. Replication in at least one independent population was achieved for 37% of cis signals and 15% of trans signals, respectively. Our results strongly support an abundance of cis-regulatory variation in the human genome. Detection of trans effects is limited but suggests that regulatory variation may be the key primary effect contributing to phenotypic variation in humans. We also explore several methodologies that improve the current state of analysis of gene expression variation.


Subject(s)
Gene Expression , Genetics, Population , Genome, Human , Genomics , Alleles , Cell Line, Tumor , Chromosomes, Human, Pair 2 , Gene Expression Profiling , Genetic Variation , Humans , Phenotype , Polymorphism, Single Nucleotide , Repressor Proteins/genetics , Transcription Initiation Site
2.
Genome Res ; 17(11): 1690-6, 2007 Nov.
Article in English | MEDLINE | ID: mdl-17895424

ABSTRACT

The goals of the human genome project did not include sequencing of the heterochromatic regions. We describe here an initial sequence of 1.1 Mb of the short arm of human chromosome 21 (HSA21p), estimated to be 10% of 21p. This region contains extensive euchromatic-like sequence and includes on average one transcript every 100 kb. These transcripts show multiple inter- and intrachromosomal copies, and extensive copy number and sequence variability. The sequencing of the "heterochromatic" regions of the human genome is likely to reveal many additional functional elements and provide important evolutionary information.


Subject(s)
Chromosomes, Human, Pair 21 , Euchromatin/genetics , Polymorphism, Genetic , Contig Mapping , Genome, Human , Humans , In Situ Hybridization, Fluorescence
3.
Genome Biol ; 8(6): R118, 2007.
Article in English | MEDLINE | ID: mdl-17578567

ABSTRACT

BACKGROUND: Gene regulation is considered one of the driving forces of evolution. Although protein-coding DNA sequences and RNA genes have been subject to recent evolutionary events in the human lineage, it has been hypothesized that the large phenotypic divergence between humans and chimpanzees has been driven mainly by changes in gene regulation rather than altered protein-coding gene sequences. Comparative analysis of vertebrate genomes has revealed an abundance of evolutionarily conserved but noncoding sequences. These conserved noncoding (CNC) sequences may well harbor critical regulatory variants that have driven recent human evolution. RESULTS: Here we identify 1,356 CNC sequences that appear to have undergone dramatic human-specific changes in selective pressures, at least 15% of which have substitution rates significantly above that expected under neutrality. The 1,356 'accelerated CNC' (ANC) sequences are enriched in recent segmental duplications, suggesting a recent change in selective constraint following duplication. In addition, single nucleotide polymorphisms within ANC sequences have a significant excess of high frequency derived alleles and high F(ST) values relative to controls, indicating that acceleration and positive selection are recent in human populations. Finally, a significant number of single nucleotide polymorphisms within ANC sequences are associated with changes in gene expression. The probability of variation in an ANC sequence being associated with a gene expression phenotype is fivefold higher than variation in a control CNC sequence. CONCLUSION: Our analysis suggests that ANC sequences have until very recently played a role in human evolution, potentially through lineage-specific changes in gene regulation.


Subject(s)
Evolution, Molecular , Gene Expression Regulation , Genome, Human , Regulatory Sequences, Nucleic Acid , Animals , Base Sequence , Conserved Sequence , Genome , Humans , Macaca , Pan troglodytes , Polymorphism, Single Nucleotide , Selection, Genetic , Sequence Analysis, DNA
4.
Science ; 315(5813): 848-53, 2007 Feb 09.
Article in English | MEDLINE | ID: mdl-17289997

ABSTRACT

Extensive studies are currently being performed to associate disease susceptibility with one form of genetic variation, namely, single-nucleotide polymorphisms (SNPs). In recent years, another type of common genetic variation has been characterized, namely, structural variation, including copy number variants (CNVs). To determine the overall contribution of CNVs to complex phenotypes, we have performed association analyses of expression levels of 14,925 transcripts with SNPs and CNVs in individuals who are part of the International HapMap project. SNPs and CNVs captured 83.6% and 17.7% of the total detected genetic variation in gene expression, respectively, but the signals from the two types of variation had little overlap. Interrogation of the genome for both types of variants may be an effective way to elucidate the causes of complex phenotypes and disease in humans.


Subject(s)
Gene Dosage , Gene Expression Regulation , Genetic Variation , Genome, Human , Polymorphism, Single Nucleotide , Cell Line , Female , Gene Deletion , Gene Duplication , Genetics, Population , Genomics/methods , Haplotypes , Humans , Linkage Disequilibrium , Male , Mutation , Nucleic Acid Hybridization , Phenotype , Regression Analysis
5.
Curr Opin Genet Dev ; 16(6): 559-64, 2006 Dec.
Article in English | MEDLINE | ID: mdl-17055246

ABSTRACT

The focus of large genomic studies has shifted from only looking at genes and protein-coding sequences to exploring the full set of elements in each genome. The explosion of comparative sequencing data has led to an increase in methodologies, approaches and ideas on how to analyze the unknown fraction of the genome, namely the non-protein-coding fraction. The main issues relate to the discovery, evolutionary analysis and natural variation of non-coding DNA, and the parameters that prevent us from fully understanding the properties of non-coding DNA.


Subject(s)
DNA/genetics , Evolution, Molecular , Regulatory Sequences, Nucleic Acid/physiology , Animals , Base Sequence , Conserved Sequence , Humans , Selection, Genetic
6.
Proc Natl Acad Sci U S A ; 102(30): 10563-8, 2005 Jul 26.
Article in English | MEDLINE | ID: mdl-16030148

ABSTRACT

Previous studies of the pericentromeric region of the human X chromosome short arm (Xp) revealed an age gradient from ancient DNA that contains expressed genes to recent human-specific DNA at the functional centromere. We analyzed the finished sequence of this human genomic region to investigate its evolutionary history. Phylogenetic analysis of >1,500 alpha-satellite monomers from the region revealed the presence of five physical domains, each containing monomers from a distinct phylogenetic clade. The most distal domain contains long interspersed nucleotide element repeats that were active >35 million years ago, whereas the four proximal domains contain more recently active long interspersed nucleotide element repeats. An out-of-register, unequal recombination (i.e., crossover) detected at the edge of the X chromosome-specific alpha-satellite array (DXZ1) may reflect the most recent of a series of punctuating events during evolution that resulted in a proximal physical expansion of the X centromere. The first 18 kb of this array has 97-99% pairwise identity among all 2-kb repeat units. To perform more detailed evolutionary comparisons, we sequenced the junction between the ancient DNA of Xp and the primate-specific alpha satellite in chimpanzee, gorilla, orangutan, vervet, macaque, and baboon. The striking conservation found in all cases supports the ancestral nature of the alpha satellite at this location. These studies demonstrate that the primate X centromere appears to have evolved through repeated expansion events occurring within the central, active region of centromeric DNA, with the newly added sequences then conferring centromere function.


Subject(s)
Centromere/genetics , Chromosomes, Human, X/genetics , DNA Repeat Expansion/genetics , Evolution, Molecular , Phylogeny , Primates/genetics , Animals , Base Sequence , Cluster Analysis , Conserved Sequence/genetics , Humans , Interspersed Repetitive Sequences/genetics , Molecular Sequence Data , Sequence Analysis, DNA
7.
Nature ; 434(7031): 325-37, 2005 Mar 17.
Article in English | MEDLINE | ID: mdl-15772651

ABSTRACT

The human X chromosome has a unique biology that was shaped by its evolution as the sex chromosome shared by males and females. We have determined 99.3% of the euchromatic sequence of the X chromosome. Our analysis illustrates the autosomal origin of the mammalian sex chromosomes, the stepwise process that led to the progressive loss of recombination between X and Y, and the extent of subsequent degradation of the Y chromosome. LINE1 repeat elements cover one-third of the X chromosome, with a distribution that is consistent with their proposed role as way stations in the process of X-chromosome inactivation. We found 1,098 genes in the sequence, of which 99 encode proteins expressed in testis and in various tumour types. A disproportionately high number of mendelian diseases are documented for the X chromosome. Of this number, 168 have been explained by mutations in 113 X-linked genes, which in many cases were characterized with the aid of the DNA sequence.


Subject(s)
Chromosomes, Human, X/genetics , Evolution, Molecular , Genomics , Sequence Analysis, DNA , Animals , Antigens, Neoplasm/genetics , Centromere/genetics , Chromosomes, Human, Y/genetics , Contig Mapping , Crossing Over, Genetic/genetics , Dosage Compensation, Genetic , Female , Genetic Linkage/genetics , Genetics, Medical , Humans , Male , Polymorphism, Single Nucleotide/genetics , RNA/genetics , Repetitive Sequences, Nucleic Acid/genetics , Sequence Homology, Nucleic Acid , Testis/metabolism
8.
Genomics ; 81(3): 249-59, 2003 Mar.
Article in English | MEDLINE | ID: mdl-12659809

ABSTRACT

Comparative genomic sequence analysis is a powerful technique for identifying regulatory regions in genomic DNA. However, its utility largely depends on the evolutionary distances between the species involved. Here we describe the screening of a genomic BAC library from the stripe-faced dunnart, Sminthopsis macroura, formerly known as the narrow-footed marsupial mouse. We isolated a clone containing the LYL1 locus, completely sequenced the 60.6-kb insert, and compared it with orthologous human and mouse sequences. Noncoding homology was substantially reduced in the human/dunnart analysis compared with human/mouse, yet we could readily identify all promoters and exons. Human/mouse/dunnart alignments of the LYL1 candidate promoter allowed us to identify putative transcription factor binding sites, revealing a pattern highly reminiscent of critical regulatory regions of the LYL1 paralogue, SCL. This newly identified LYL1 promoter showed strong activity in myeloid progenitor cells and was bound in vivo by Fli1, Elf1, and Gata2-transcription factors all previously shown to bind to the SCL stem cell enhancer. This study represents the first large-scale comparative analysis involving marsupial genomic sequence and demonstrates that such comparisons provide a powerful approach to characterizing mammalian regulatory elements.


Subject(s)
Chromosome Mapping , DNA-Binding Proteins/genetics , Marsupialia/genetics , Neoplasm Proteins/genetics , Phylogeny , Amino Acid Sequence , Animals , Base Sequence , Basic Helix-Loop-Helix Transcription Factors , DNA , DNA-Binding Proteins/chemistry , Models, Genetic , Molecular Sequence Data , Neoplasm Proteins/chemistry , Promoter Regions, Genetic , Sequence Homology, Amino Acid , Sequence Homology, Nucleic Acid
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