- Research article
- Open Access
A comprehensive functional analysis of tissue specificity of human gene expression
- Zoltán Dezső†1Email author,
- Yuri Nikolsky†1,
- Evgeny Sviridov2,
- Weiwei Shi1,
- Tatiana Serebriyskaya2,
- Damir Dosymbekov2,
- Andrej Bugrim1,
- Eugene Rakhmatulin1,
- Richard J Brennan1,
- Alexey Guryanov2,
- Kelly Li3,
- Julie Blake3,
- Raymond R Samaha3 and
- Tatiana Nikolskaya2
© Dezső et al; licensee BioMed Central Ltd. 2008
- Received: 29 October 2008
- Accepted: 12 November 2008
- Published: 12 November 2008
In recent years, the maturation of microarray technology has allowed the genome-wide analysis of gene expression patterns to identify tissue-specific and ubiquitously expressed ('housekeeping') genes. We have performed a functional and topological analysis of housekeeping and tissue-specific networks to identify universally necessary biological processes, and those unique to or characteristic of particular tissues.
We measured whole genome expression in 31 human tissues, identifying 2374 housekeeping genes expressed in all tissues, and genes uniquely expressed in each tissue. Comprehensive functional analysis showed that the housekeeping set is substantially larger than previously thought, and is enriched with vital processes such as oxidative phosphorylation, ubiquitin-dependent proteolysis, translation and energy metabolism. Network topology of the housekeeping network was characterized by higher connectivity and shorter paths between the proteins than the global network. Ontology enrichment scoring and network topology of tissue-specific genes were consistent with each tissue's function and expression patterns clustered together in accordance with tissue origin. Tissue-specific genes were twice as likely as housekeeping genes to be drug targets, allowing the identification of tissue 'signature networks' that will facilitate the discovery of new therapeutic targets and biomarkers of tissue-targeted diseases.
A comprehensive functional analysis of housekeeping and tissue-specific genes showed that the biological function of housekeeping and tissue-specific genes was consistent with tissue origin. Network analysis revealed that tissue-specific networks have distinct network properties related to each tissue's function. Tissue 'signature networks' promise to be a rich source of targets and biomarkers for disease treatment and diagnosis.
- Gene Ontology
- Cluster Coefficient
- Average Short Path
- Giant Strong Component
- Comprehensive Functional Analysis
The issue of tissue and cell-type specificity of gene expression is central to human biology and biomedicine. It impacts such fundamental problems as tissue ontogenesis, evolution and carcinogenesis. It is generally believed that the most relevant disease biomarkers and drug targets predominantly are found among proteins specific for the tissue the disease affects. In 1965 Watson et al. described genes universally expressed to maintain cellular functions as 'housekeeping' (HK) genes . Comprehensive experimentation in this area was, however, limited until, in the 1990s, microarrays enabled 'genome-wide' snapshots of gene expression. Numerous studies on tissue-specific expression have since been published [2–8], identifying between 451 and 1789 genes  as a HK core on different microarray platforms. There is no standard method for assigning a gene as HK, and no comprehensive functional analysis of HK and tissue-specific genes has previously been done.
Here we report the identification of 2374 HK genes, based on a novel study of gene expression in 31 human tissues on a whole-genome ABI array. We set up a definitive 'HK baseline' for gene expression across tissues, and compared previously published HK data sets with ours. We also identified gene sets uniquely expressed in individual tissues and groups of tissues, and generated tissue-specific merged metabolic/signaling 'signature networks'. Both HK and tissue-specific genes were subjected to a comprehensive, three-phase functional analysis, including gene set enrichment across four ontologies, network topology analysis and tissue-specific network analysis. We clustered tissues into groups according to expression patterns and network parameters, and revealed associations between HK and tissue-specific genes with human diseases and drug targets.
Definition of housekeeping and tissue-specific genes
Number of housekeeping and tissue-specific genes
Peripheral blood lymphocytes
Average, somatic tissues
An alternative method, using the Student's t-test, was also applied to identify tissue-specific genes. Functional analysis showed striking similarities in the biological processes encompassed in the genes specific to each tissue between the t-test and the threshold-based methods (description of method and results in Additional file 3).
Ontological analysis of housekeeping and tissue-specific genes
Enrichment analysis of housekeeping and three selected tissue-specific gene sets.
Canonical pathways maps
CREM signaling in testis
Tyrosine metabolism (dopamine)
Glycolysis and gluconeogenesis
TGF, WNT and cytoskeletal remodeling
ATM/ATR regulation of G2/M checkpoint
Formation of Sin3A and NuRD complexes and their role in transcription regulation
Regulation of CDK5 in CNS
Role of APC in cell cycle regulation
Cortisone biosynthesis and metabolism
TGF, WNT and cytoskeleton remodeling
Role of Nek in cell cycle regulation
Rap1A regulation pathway
Androstenedione and testosterone biosynthesis and metabolism
Regulation activity of EIF4F
Androgen receptor nuclear signaling
Non-genomic (rapid) action of androgen receptor
WNT signaling pathway
Receptor-mediated HIF regulation
Insulin regulation of fatty acid metabolism
Androgen receptor nuclear signaling
Role of tetraspanins in the integrin-mediated cell adhesion
Rap1B regulation pathway
WNT signaling pathway
Nucleocytoplasmic transport of CDK/Cyclins
TGF, WNT and cytoskeletal remodeling
Regulation activity of EIF2
Signal transduction_Visual perception
Transmission of nerve impulse
Cell adhesion cadherins
Reproduction_GnRH signaling pathways
Signal transduction_CREM pathway
Development neurogenesis in general
Development_Neurogenesis in general
Reproduction_Male sex differentiation
Signal transduction NOTCH signaling
Translation_Regulation of initiation
Signal transduction_Androgen receptor nuclear signaling
Signal transduction_Androgen receptor signaling cross talk
Protein folding_Folding in normal condition
Signal transduction_CREM pathway
Immune_Phagosome in antigen presentation
Signal transduction_Neuropeptides signaling pathway
Protein folding_Protein folding nucleus
Cell adhesion_Integrin priming
Development ossification and bone remodeling
Protein folding_Response to unfolded protein
Translation_Regulation of initiation
Signal transduction_Visual perception
Protein folding_ER and cytoplasm
Reproduction_Male sex differentiation
Cell adhesion amyloid proteins
Sensory perception of light stimulus
Cellular metabolic process
Smooth muscle differentiation
Macromolecule metabolic process
Male gamete generation
Primary metabolic process
Detection of visible light
Male gonad development
Macromolecule biosynthetic process
Detection of light stimulus
Embryonic epithelial tube formation
Cellular protein metabolic process
Detection of abiotic stimulus
Development of primary male sexual characteristic
Cellular macromolecule metabolic process
Germ cell development
Protein metabolic process
Detection of light stimulus during visual perception
Detection of light stimulus during sensory perception
Development of primary sexual characteristics
Dopamine biosynthetic process from tyrosine
Neoplasm by site
Adrenal gland disease
Genetic disease, inborn
Adrenal cortex disease
Digestive systems neoplasm
Ciliary motility disorders
Adrenal cortex neoplasm
Adrenal gland neoplasm
Lysosomal storage disease
Eye diseases, hereditary
Carcinoma, basal cell
Neoplasm, basal cell
Autonomic nervous system diseases
Using the GSEA procedure  across the same ontologies produced similar distributions (data not shown). Importantly, HK sets from the previously published studies were generally enriched in similar categories to our own HK set across all four ontologies. For example, oxidative phosphorylation, cytoskeleton remodeling, translation and macromolecule biosynthetic process were among the top-scoring maps and processes for all HK sets (Additional file 4). Functional analysis of the unique parts of HK sets showed differences among top-scoring processes and maps. Our unique (not yet identified) HK genes showed enrichment with metabolic, translation and cell-cycle processes, validating the part of the HK set which was not identified by previous studies. Unique parts of some of the other sets, however, showed enrichment of more specific processes such as immune, inflammatory and cardiac-specific processes (Additional file 6).
Network properties and interactome analysis of HK and tissue-specific genes
We analyzed the 'interaction space' of the protein products of HK and tissue-specific genes in three steps. First, we calculated topological properties of the 'interactomes', such as degree of connectivity, average shortest path and clustering coefficient . Second, we evaluated the interactome structure by parsing the interactions into three components (IN, OUT and giant strong component, GSC) using the 'bow-tie' classification of Broder et al. . Third, we divided HK and tissue proteins into protein classes and calculated relative enrichment across particular classes. For topological analysis, we used the directional protein-protein interaction content in MetaCore™ (GeneGo Inc.). We also analyzed, for reference, four previously published HK gene sets.
Network topology parameters were also used for tissue clustering. The topological distances between all possible tissue pairs were calculated as the ratio of the average shortest paths between proteins belonging to different tissues to the average shortest paths between proteins from the same tissue. Standard hierarchical clustering  was applied to generate the tissue tree. Interestingly, some of the functionally related tissues such as brain, fetal brain, retina and spinal cord were grouped together and characterized by very similar average shortest paths (Additional file 10).
An interactome can be divided into three structural parts, or 'components' . The GSC is the most densely connected part of the network, characterized by the property that any two nodes can be connected through directed paths in both directions. Directed paths from the GSC lead out to the OUT component and paths from the IN component go in to the GSC (Figure 4C, upper panel). In order to facilitate interpretation, the interactions were divided by 16 mechanisms (Additional file 11). The IN component is enriched with 'outgoing' interactions such as ligand-receptor binding interactions, which occur five times more frequently in IN than in GSC, and ten times more frequently than in the OUT component. Interactions between IN and GSC components also have five times more ligand-receptor interactions than between GSC and OUT. The GSC component predominantly features 'transcriptional regulation' interactions, which appear ten times more often in the GSC than the OUT, and six times more often than the IN components. The OUT component is enriched with 'incoming' interactions such as transcription factor target. Indeed, 48% of interactions between the GSC and OUT are transcription regulation compared with 4% of interaction between IN and GSC being transcription regulation. The GSC encompassed around 50% of the HK network. Overall, the fraction of HK genes was larger in the GSC (p < 10-5) and slightly lower in the IN and OUT component than a random gene set of the same size (Figure 4C). This suggests that HK proteins comprise a significant proportion of signal transduction interactions. Mammary gland and tonsil were enriched in GSC (p < 0.08 and p < 0.14); intestine and adult kidney in OUT component (p < 0.03 and p < 0.07), and skin (p < 0.1) in IN component (Figure 4C, Additional file 12).
Next, all HK and tissue-specific sets were divided into protein classes according to the MetaCore protein classification schema (Additional file 13). Enrichment in proteins of a certain class was then calculated from the hypergeometric distribution. The distribution of protein classes in the global interactome was used as a reference (Methods). HK proteins were enriched in enzymes (p < 10-8). Intestine, liver and adrenal gland featured the highest fraction of enzymes. Fetal tissues were highly enriched in transcription factors, and retina and brain in membrane receptors (Figure 4B). Such distributions make intuitive biological sense, and both network structure and protein class enrichment were consistent with each other.
Clustering tissues based on gene expression patterns
Drug target distribution between housekeeping and tissue-specific genes
We compared the distribution of drug targets between HK and tissue-specific protein sets. Two sets of drug targets were compiled: 'therapeutic targets' – a set of 104 direct protein targets of commercially available drugs, and 'xenobiotic targets' – 518 proteins known to interact with xenobiotics. Therapeutic drugs are defined as key proteins or genes directly affected by a marketed or withdrawn drug from the market. Xenobiotic targets are proteins and genes known for physical interactions with a large set of bioactive compounds including drugs, drug candidates and lead compounds.
On average, therapeutic targets were twice as prevalent among tissue-specific proteins than HK proteins (3.3% and 1.5% of all proteins, correspondingly) (Additional file 15). Therapeutic targets comprised as much as 25% of mammary gland and thymus-specific proteins. The distribution of xenobiotic targets was not essentially different between HK and the sum of tissue-specific proteins, with some 1.7% of HK proteins and 2.3% of tissue-specific proteins being xenobiotic targets. Some tissues, however, were highly enriched with xenobiotic targets. For instance, over 10% of proteins specific for mammary gland, ovary, retina, small intestine and spinal cord were identified as xenobiotic targets (Additional file 15).
The definition of a 'housekeeping' or 'universally-expressed' gene is not settled. Suggested approaches vary from an estimated 10% of all genes  to transcript copy number  to using 'present' calls . Elisenberg and Levanon  assumed that HK genes are highly expressed 'by nature' and, therefore, must be selected for shorter introns. We followed the original 'common-sense' proposal of Watson et al.  to define 2374 genes as HK because their transcripts were detected in all 31 human tissues tested, at a signal-to-noise ratio ≥ 10, which we believe to be a relatively stringent cut-off (technical analysis of platform sensitivity at ABI has indicated that a signal-to-noise ratio of ≥ 3 is sufficient to determine 'presence' of a transcript with a confidence of 99.9%. This set constitutes 8.2% of human genes based on the latest National Center for Biotechnology Information genome release http://0-www.ncbi.nlm.nih.gov.brum.beds.ac.uk/mapview/stats/BuildStats.cgi?taxid=9606&build=36&ver=2.
Tissue-specific gene sets, comprising genes uniquely expressed in individual tissues by the SN10 criterion, averaged 43 genes for somatic tissues, and 485 mostly meiosis-specific genes in testis. The tissue specificity distribution is represented by a bimodal distribution with two peaks at 1 and 31 corresponding to tissue-specific and HK genes (Additional file 16). Interestingly, the female reproductive organ, ovary, expressed many fewer unique genes, probably due to the fact that ovary consists mainly of diploid tissue compared with the haploid-rich testis, as ovary produces far fewer eggs than testis does sperm.
There is continuing debate in gene expression analysis over how to best identify genes differentially expressed between treatment conditions, disease states and so on. Arbitrarily applied cut-offs in relative magnitude of expression (fold-change) and statistical measures such as ANOVA and t-test are commonly used [19, 20]. Renewed debate was sparked recently [21, 22] following publication of the results of the Microarray Quality Control Consortium research efforts . It was shown that a combination of non-stringent statistical cut-offs and fold-change ranking of gene lists resulted in improved concordance between measurements made using different expression analysis technologies, an approach likely therefore to give the most accurate biological 'answer'.
We applied both signal level (signal-to-noise) and statistical (t-test) methods to determine tissue specificity of gene expression. Although the resulting datasets did not overlap well in gene content (6% on average), they were highly similar by functional analysis. Importantly, the intersections between distributions of entities within functional ontologies for SN10 and t-test sets were substantially larger than between genes (Additional file 3), suggesting that the two methods both select biologically relevant genes, which can be interconnected on pathways and networks. Further, despite incomplete overlap between our HK set and four other previously published HK sets, all gave very similar results in ontological enrichment analyses. These observations support the use of functional descriptors (pathways, networks, ontological categories and so on) as tools for quantitative characterization of conditional gene expression .
HK and tissue-specific gene sets were subjected to comprehensive functional analysis in three steps: enrichment analysis across functional ontologies using hypergeometric distribution  and GSEA methods ; local interactome analysis; generation of signaling/metabolic networks using HK and tissue-specific gene content as input nodes. We used multiple functional ontologies for enrichment analysis: GO processes, GG processes, disease categories and canonical pathway maps. Each ontology is established using different criteria and reveals a different aspect of cellular functionality. Canonical pathways are experimentally confirmed multi-step chains of reactions. GO and GG processes differ, as connectivity is established at the level of functional association (GO processes) or binary interactions (GG processes). Diseases and disease network ontologies represent pathways involved in pathological processes, largely derived from literature data linking network objects (genes, proteins, metabolites) to disease.
Ontology enrichment showed that HK genes, indeed, were enriched in vital cellular functions such as oxidative phosphorylation, ubiquitin-proteasomal proteolysis, translation and major pathways of endogenous metabolism. Importantly, many essential processes involve a large number of interconnected proteins (typically several hundred), and many of these genes belong to our HK set, confirming the functional integrity and completeness of the HK set.
Recently it was shown in line with our results that the number of HK genes is larger than previously reported [4, 25]. Our findings are complementary to the high-resolution study based on expressed sequence tag (EST) profiling reported by Zhu et al. . Indeed, both methods have advantages and drawbacks, EST data although have potentially higher resolution, suffers from poor annotation and low sampling depth . Our results are very consistent throughout the 31 tissues and are well confirmed by enrichment analysis in multiple functional ontologies. We expect that higher resolution data would not alter the main conclusions of the enrichment and network analysis.
Ontology enrichment in tissue-specific genes was strikingly different from HK genes, and in most cases strikingly consistent with the tissue's function. Retina genes were enriched with such processes as visual perception, detection of visible light, detection of light stimulus and eye disease-related genes, and testis genes scored highest for reproductive processes, cell cycle, cell division and male reproductive diseases, for example. Importantly, almost all tissues featured a high level of consistency between the highest-scored categories in different ontologies. Further, consistency was observed whether hypergeometric p-values or GSEA analyses were employed. This important observation adds confidence to the conclusions drawn from the analysis of tissue-specific gene expression, and can be applied similarly to other studies of differentially expressed genes and proteins. It also will facilitate the development of a comprehensive set of 'meta-ontologies' derived from an understanding of the interplay and crossover between the different types of ontological categories available, leading to improved understanding of biological systems, and the identification of biologically meaningful biomarkers and new therapeutic targets.
Network analysis  showed that a large part of HK genes belonged to the most interconnected GSC core of the global interactome, with equal representation of 'in' and 'out' interactions. On the other hand, tissue-specific genes varied greatly in network component composition. Skin and fetal brain were enriched with 'IN' component, consistent with a larger proportion of ligand-receptor interactions in these tissues. Not surprisingly, these tissues featured a large fraction of receptors in the protein class enrichment test. In comparison, 'effector' organs such as intestine, liver and kidney, were enriched with 'OUT' interactions and enzymes. A transcription factor-enzyme pair represents a typical directed 'out' interaction – a final step in delivering a signal from stimulus to core 'effectors' such as endogenous metabolic pathways. These findings are in line with the 'bow-tie' structure of metabolic networks, which ensures robustness of major biological functions , and is needed for coordinated response to stimuli and perturbation .
'Multi-dimensional' functional analysis of gene expression data adds to the ongoing debate on proper statistical procedures for gene set selection. A 'rule of thumb' opinion is that only gene sets and distributions with low p-values (typically, p < 0.01) should be considered valid, although such ad hoc cut-offs may eliminate many condition-relevant genes from analysis. Functional analysis provides a different level of validation for such datasets by consideration of functional biological units. For instance, the retina-specific gene set is enriched in vision-related pathways, GO and GG ontologies, and diseases. The same set is enriched with OUT network component, and the protein class 'receptors'. Self-assembling retina-specific networks reconstruct rhodopsin-stimulated signal transduction and key steps in the metabolism of rhodopsin and its co-factors. Although the retina gene set is too small to achieve p-values < 0.01 in most of these analyses, the combination of independent functional evidence builds a strong case for its relevance and importance as a highly likely source of specific biomarkers for eye conditions and ophthalmic drug response. The comprehensive biological interaction data in MetaCore allows multiple 'high-content' data types to be mapped onto networks. Gene expression data, proteomic, single nucleotide polymorphism and metabolomic data all can be addressed, visualized and used in network construction and analysis, independently or in concert , making it a universal tool for studies on eye and other diseases.
Tissue-specific gene sets (and, therefore, networks) were twice as enriched in drug targets as the HK set. 'Therapeutic' targets comprised up to 25% of mammary gland and thymus-specific proteins. Most of the identified tissue-specific drug target genes are targets to drugs whose mechanism are consistent with the tissues. For example, three brain-specific proteins identified to have at least one drug target are GABA-A receptor beta-2 subunit, Na (V) I alpha and SCN10A. GABA-A receptor beta-2 subunit is a target for clomethiazole (sedative and anticonvulsant), Na (V) I alpha is a target for drugs such as levetiracetam (epilepsy), tetrodotoxin (anesthetics), toprimate (anticonsulvant) and SCN10A is target for bupivacaine racemic (anesthetics) and lidocaine (anesthetics).
Tissue-specific proteins and their pathways and networks are therefore a potentially rich source of targets and biomarkers for disease treatment and diagnostics. The addition of data on which network components are detectable in blood and other readily accessible body liquids makes tissue-specific networks exceptionally attractive for the identification of putative biomarkers of tissue-specific disease, drug-response or toxicity.
RNA from 31 normal human tissue RNAs (Table 1) was purchased from Clontech (Palo Alto, CA) while RNA from UHR (Universal Human Reference) was purchased from Strategene (San Diego, CA). All RNA samples were analyzed on the Agilent 2100 Bioanalyzer for RNA quality control. Three technical replicates were included for each of the tissue sample.
The Applied Biosystems Human Genome Survey Microarray (P/N 4337467) contains 31,700 60-mer oligonucleotide probes representing 27,868 individual human genes. Digoxigenin-UTP labeled cRNA was generated and amplified from 1 μg of total RNA from each sample using Applied Biosystems Chemiluminescent RT-IVT Labeling Kit v 1. 0 (P/N 4340472) according to the manufacturer's protocol (P/N 4339629). Fifteen micrograms of DIG-labeled cRNA was hybridized for 16 hrs at 55°C and chemiluminescence detection, image acquisition and analysis were performed using Applied Biosystems Chemiluminescence Detection Kit (P/N 4342142) and Applied Biosystems 1700 Chemiluminescent Microarray Analyzer (P/N 4338036) following the manufacturer's protocol (P/N 4339629). Images were auto-gridded and the chemiluminescent signals were quantified, background subtracted, and finally, spot- and spatially-normalized using the Applied Biosystems 1700 Chemiluminescent Microarray Analyzer software v 1. 1 (P/N 4336391). Probe signals were normalized using the Limma method . The gene expression data is publicly available at GEO public repository website. (GSE7905).
Identification of HK and tissue-specific genes
A 'stringent' set of HK genes expressed in each of the 31 tissues was identified by applying cut-off to the ABI-calculated signal-to-noise (S/N) for each probe. The S/N is a metric that captures the confidence of the measurement 'detectability' above all known sources of noise. S/N is commonly used to bin genes or probes as 'Present' or 'Absent' at a desired level of confidence. Since the S/N expresses the number of standard deviations, the associated confidence can be looked up from a probability table for a normal distribution. For example, signals with S/N ≥ 3 have > 99.9% confidence in the measurement. For our purposes in determining whether a gene was expressed in a given tissue, we additionally took into account the inflection points where the slope of the S/N curve significantly changes. We applied the threshold across all three replicate hybridizations on a probe-by-probe basis to identify the genes expressed in each tissue with a high level of confidence. The overlap between all 31 sets, that is, genes consistently expressed in all tissues, defines the HK set (more details in Additional file 17). Tissue-specific genes were defined as those uniquely expressed in a single given tissue at a S/N ≥ 10. Genes expressed in highly related tissue pairs were also defined as tissue specific for some analyses.
Degree of nodes
The number of links connected to a node gives the node's degree. Since many real networks are directed, nodes are characterized by in and out-degree, giving the number of incoming and outgoing interactions.
Average shortest path
The shortest distance between two nodes is the number of links along the shortest path. The average shortest path is the average over the shortest paths for all node pairs in the network. When we calculate the shortest paths for a subset of nodes in the network we consider also paths crossing through nodes that are not part of the subset.
Average clustering coefficient
where n i is the number of links among the k i neighbors of node i. As k i (k i -1)/2 is the maximum number of such links, the clustering coefficient is a number between 0 and 1. The average clustering coefficient is obtained by averaging over the clustering coefficient of individual nodes. A network with high clustering coefficient is characterized by highly connected sub-graphs.
which gives the probability of having k or more marked elements in a sample of size n by random selection.
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