96 research outputs found
Supplementary material.for manuscript entitled "Dysregulation of Hypothalamic Gene Expression and the Oxytocinergic System by Soybean Oil Diets in Male Mice"
No full textThis file contains Supplementary Figures 1-3 and Supplementary Tables 1-9 for the manuscript entitled "Dysregulation of Hypothalamic Gene Expression and the Oxytocinergic System by Soybean Oil Diets in Male Mice" Authors:Poonamjot Deol, Elena Kozlova, Matthew Valdez, Catherine Ho1, Ei-Wen Yang3, Holly Richardson, Gwendolyn Gonzalez, Edward Truong, Jack Reid, Joseph Valdez, Jonathan R. Deans, Jose Martinez-Lomeli, Jane R. Evans, Tao Jiang, Frances M. Sladek, Margarita C. Curras-CollazoCorresponding author requests:Dr. Margarita [email protected] approval and consent to participate:Care and treatment of animals was in accordance with guidelines from and approved by the University of California, Riverside Institutional Animal Care and Use Committee (AUP #20140014 and #20140017).
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Role of the Maternal Liver in Lactating Mice
No full textLactation brings about numerous maternal physiological and metabolic changes in order to sustain viable offspring. The liver plays a role in meeting the high energetic and metabolic needs of lactation as it is a key player in various biological processes that include lipid metabolism and homeostasis. A growing body of evidence suggests that the metabolic and physiological changes that lactation brings to the nursing mother results in a maternal profile that lowers the incidence of metabolic diseases. In this study, we examine in vivo and gene expression profiling data of fasted, age-matched virgin (V), non-lactating (NL), and lactating (L) C57Bl/6 mice in an attempt to understand the role the maternal liver plays in lactation in a global context. Our model allows us to examine the long term effects of lactation, since both the lactating and non-lactating mice have previously nursed pups. In vivo results highlight maternal adaptations to lactation that include rapid weight loss, increased liver weight, increased plasma triglyceride levels, and decreased hepatic triglyceride storage. Gene expression profiling reveals molecular signatures of different classes of genes that may explain the resulting maternal adaptations to lactation. Our model suggests a highly metabolically active liver that plays a role in supplying the energy that the lactating mammary gland needs, by synthesizing triglycerides and secreting them into the blood stream, thus making them available to the lactating mammary gland
The Influence of Transcription Factor Competition on the Relationship between Occupancy and Affinity
No full textTranscription factors (TFs) are proteins that bind to specific sites on the DNA and regulate gene activity. Identifying where TF molecules bind and how much time they spend on their target sites is key to understanding transcriptional regulation. It is usually assumed that the free energy of binding of a TF to the DNA (the affinity of the site) is highly correlated to the amount of time the TF remains bound (the occupancy of the site). However, knowing the binding energy is not sufficient to infer actual binding site occupancy. This mismatch between the occupancy predicted by the affinity and the observed occupancy may be caused by various factors, such as TF abundance, competition between TFs or the arrangement of the sites on the DNA. We investigated the relationship between the affinity of a TF for a set of binding sites and their occupancy. In particular, we considered the case of the transcription factor lac repressor (lacI) in E.coli, and performed stochastic simulations of the TF dynamics on the DNA for various combinations of lacI abundance and competing TFs that contribute to macromolecular crowding. We also investigated the relationship of site occupancy and the information content of position weight matrices (PWMs) used to represent binding sites. Our results showed that for medium and high affinity sites, TF competition does not play a significant role for genomic occupancy except in cases when the abundance of the TF is significantly increased, or when the PWM displays relatively low information content. Nevertheless, for medium and low affinity sites, an increase in TF abundance (for both cognate and non-cognate molecules) leads to an increase in occupancy at several sites. © 2013 Zabet et al
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The Role of Nuclear Receptors in Tissue-Specific Gene Expression: The Impact of Genetic Variation on DNA Binding
No full textNuclear receptors (NRs) are ligand-sensitive transcription factors that regulate a wide array of biological processes including development, metabolism, and circadian rhythms. All NRs share a common protein structure, including highly conserved DNA binding domains and a highly variable N-terminal A/B domain, and are very popular drug targets. To better understand the role of alternative A/B domains between NR isoforms and the impact of genetic variation on gene expression in the liver, we employed two experimental approaches. The NR hepatocyte nuclear factor 4α (HNF4α), a master regulator of liver-specific gene expression, is regulated by two promoters (P1 and P2) in the liver resulting in proteins with different A/B domains. P1-HNF4α is expressed in fetal and normal adult liver while P2-HNF4α is expressed only in the fetal liver and in liver cancer. We compared wildtype mice, which express only HNF4α1 (P1) in the adult liver, to exon-swap mice that express only HNF4α7 (P2) for global changes in gene expression (RNA-seq), chromatin binding (ChIP-seq), and unique protein interactions (RIME). The results show that P1- and P2-HNF4α isoforms differentially regulate hundreds of transcripts in the adult liver, including the NR CAR (Nr1i3), and may be recruited differentially to non-HNF4α binding sites by unique protein interactions. They also exhibit altered metabolic pathways, especially cytochrome P450 (Cyp) genes. All told, the results show that changes in just 16-30 amino acids in the AF-1 region of an NR can have profound effects on gene expression. Utilizing protein binding microarrays (PBM), we can measure the DNA binding affinity of a given NR against both alleles of 125,000 genetic variants in a single experiment to probe for affinity altering SNPs (aaSNPs). By mining SNPs from ChIP-seq peaks and eQTLs from the GTEx project, we have identified thousands of aaSNPs, hundreds of which show significant correlation to changes in gene expression within their regulatory network. Analysis of aaSNPs from GWAS studies associated with Alzheimer’s disease identified a large number of genetic variants that can alter the DNA binding affinity of PPARɣ in the APOE locus. Additionally, we show the power of the PBMs to validate many aaSNPs derived from in vivo analysis and suggest a role for the PBM technology in characterizing how genetic diversity may play a role in personalized medicine
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Genome-Wide Analysis of the Impact of Diet on Liver and Intestines in Mouse and SNPs in Human HNF4a Binding Sites
No full textThe use of next-generation sequencing technology has been extremely useful for genome-wide analysis in many different organisms. For example, transcriptomic analysis based on RNA-seq can identify all changes in gene expression in a given tissue in a single experiment. Other types of experiments, such as ChIP-seq, allow mapping of transcription factor binding sites across the genome. Much of the work in this dissertation focuses on the transcription factor hepatocyte nuclear factor 4a (HNF4a) which is a member of the nuclear receptor superfamily of ligand-dependent transcription factors and abundantly expressed in the liver and intestines. HNF4a has been linked to several diseases including diabetes, liver and colon cancer, inflammatory bowel disease and others. The expression of HNF4a is driven by two promoters (P1 and P2) which result in the expression of 12 different isoforms. Additionally, HNF4a has as its endogenous ligand an essential fatty acid (linoleic acid, LA) that must be obtained from the diet and is known to play a role in gluconeogenesis during fasting. Therefore, we examine fasted vs fed conditions as well as high fat diets with different amounts of LA on gene expression in the liver and intestines, respectively. Finally, HNF4a target genes have been extensively studied and mutations in HNF4a binding sites in regulatory regions of select target genes associated with disease have been identified. However, to date, there has been no systematic approach to identify variants in HNF4a binding sites of target genes on a genome-wide scale.In Chapter 1 of this dissertation, we provide an introduction to the biological and research problems addressed in the remainder of the dissertation and review the relevant literature. In Chapter 2, we analyze transcriptomic (RNA-seq) data from male mice fed three different high fat diets (HFDs) with different amounts of LA from four different tissues across the mouse intestinal tract. We found that different portions of the intestines have unique gene profiles, especially in terms of nuclear receptor signaling, xenobiotic and drug metabolism, and intestinal epithelial barrier function. We found that different types of HFDs impact gene expression in the intestinal tract in different ways, including genes linked to diseases such as inflammatory bowel disease and colon cancer. A network analysis revealed that mice fed the HFDs had altered expression of intestinal genes involved in crucial body functions such as the immune system and the intestinal microbiome which could facilitate bacterial and viral infections such as SARS-CoV-2. To our knowledge, this is the most comprehensive dataset including multiple diets and multiple parts of the intestines and should provide an excellent resource for the scientific community for some time to come.
In Chapter 3, we compared the impact of fasting and HNF4a isoforms on liver gene expression and alternative splicing, comparing and contrasting two RNA-seq datasets from male and female mice. We also compared wild type mice (express predominantly P1-HNF4a isoforms) to exon swap mice (a7HMZ) which express only the P2 isoforms of HNF4a which are typically not expressed in the adult liver. We found that a 12-hour fast has a significant effect on alternative splicing and that the P2-HNF4a isoforms seem to play a role. Interestingly, there was a different pattern of alternative splicing in female livers.
In Chapter 4, we analyze the impact of single nucleotide polymorphisms (SNPs) on HNF4a binding sites using publicly available datasets of HNF4a ChIP-seq (chromatin immunoprecipitation) from human liver and the liver cancer cell line HepG2 which expresses HNF4a and exhibits a hepatocyte phenotype. For this purpose, we trained a support vector machine (SVM) to predict binding affinity scores based on DNA sequences known to bind HNF4a from protein binding microarray (PBM) data. This model allowed us to identify 10 putative affinity altering SNPs (aaSNPs) in the human liver HNF4a ChIP-seq and six in the HepG2 ChIP-seq that impact the binding of HNF4a to the chromatin. Additionally, some of these identified SNPs were found in genes related to cancer, suggesting a potential role in personalized medicine. These results present a proof concept of affinity disruption in binding between HNF4a and some target genes in a genome-wide analysis.
Finally, in Chapter 5, we provide an example of how transcriptomic data could be used to generate new biological hypotheses and test them. Additionally, we provide future directions for Chapter 3 and Chapter 4
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The Role of the P1 and P2 Promoter-Driven HNF4a Isoforms in Cellular Proliferation and Differentiation in Human Colon Cancer and Mouse Embryonic Stem Cells
No full textCellular proliferation and differentiation are critical events in normal development and cancer. Despite decades of research, much remains to be learned about how cells transition between the two states. To decipher one aspect of this switch, we focused on the transcription factor, Hepatocyte Nuclear Factor (HNF) 4 alpha. HNF4a is a nuclear receptor that is important in development and in maintaining the homoeostasis of the adult liver and colon. There are multiple isoforms of the HNF4a that are generated by alterative promoter (P1 and P2) usage and 3' splicing events in different tissues. Both P1 and P2-HNF4a isoforms are expressed in the adult colon, while the P1-HNF4a is expressed in the adult liver. Others have shown that P1-HNF4a is downregulated in cancer, whereas P2-HNF4a is upregulated in hepatocellular carcinoma and colorectal cancer. This would suggest that P1-HNF4a is tumor suppressive, while P2-HNF4a may act as an oncogene although a mechanism has not been elucidated. One potential mechanism could be through a differential interplay with the Wnt/beta-catenin/TCF pathway, which is activated in many cancers including liver and colon. To determine whether HNF4a and TCF4 cross-talk to control the switch between proliferation and differentiation and to elucidate the role of the HNF4a isoforms in early development and cancer, we generated Tet-On inducible systems that express either HNF4a2 (P1) or HNF4a8 (P2) under the control of doxycycline in human colon cancer and mouse embryonic stem cells. We characterized the lines to look for morphological and functional differences between the isoforms. We performed RNA-Seq and ChIP-Seq on the HCT116 inducible lines to identify any changes in gene expression and regulation and compared the HNF4a2 and HNF4a8 lines to determine functional differences. Although we found some functional redundancy, there are discrete differences. HNF4a2 suppresses tumor growth, inhibits cellular proliferation, and competes with TCF4 for regulation of target genes more effectively than HNF4a8. Similarly, we also found that HNF4a2 decreases cell numbers more than HNF4a8 in the mES inducible lines. Our findings provide insight into the distinct role of the P1- and P2-HNF4a in cancer and normal development
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Investigation of Transcription Factor Binding Sequences and Target Genes using Protein Binding Microarrays
No full textThis thesis describes the investigation of binding rules and DNA binding sequences for several transcription factors (TFs). We develop Protein Binding Microarrays (PBMs) to study the interactions between TFs and in vitro and we use a support vector machine (SVM) algorithm to capture these interactions in silico. We then apply this methodology to study the binding of TFs to promoters and repetitive sequences in a genomewide fashion. In Chapter 2, we thoroughly investigate HNF4α DNA binding interactions using PBMs. We investigate binding specificities for various isoforms and species of HNF4α. We then use PBMs to rank ~ 4,000 HNF4α binding sequences in order of binding affinity. Using this training set we identify/predict novel HNF4α binding sequences and rules, and from these rules we generate a model for HNF4α binding. We then use this large dataset, in combination with ChIP-on-chip and RNAi followed by an expression profiling to identify hundreds of novel HNF4α direct target genes. In Chapter 3, we identify HNF4α association with Alu repeats, a novel finding. We investigate HNF4α binding to Alu sequences in in vitro and in vivo in the promoters of HNF4alpha-regulated genes, and thus reveal a novel association between HNF4α and Alu repeats.Finally in Chapter 4, we leverage the PBM technology to investigate the binding properties of transcription factors COUP-TF2 and TCF-1. We identify many sequences that bind both HNF4αand TCF-1 and those bind both HNF4α and COUP-TF2. This finding suggests competition between these TFs on the promoters of their target genes. Additionally, we investigate the effect of coregulator PGCα and the effect of the endogenous ligand linoleic acid HNF4α DNA binding. This study significantly advances our knowledge of binding sequences, binding motifs, target genes, and transcriptional regulation for several transcription factors, HNF4α, COUP-TF2 and TCF-1. It also sheds light on evolution of HNF4α binding sequences through Alu repetitive elements. It suggests a strong framework for comprehensive investigation of transcriptional regulation in mammalian systems for other transcription factors
2A. Hepatocyte nuclear factor-4 receptors in GtoPdb v.2023.1
No full textThe nomenclature of hepatocyte nuclear factor-4 receptors is agreed by the NC-IUPHAR Subcommittee on Nuclear Hormone Receptors [9, 3]. While linoleic acid has been identified as the endogenous ligand for HNF4α its function remains ambiguous [75]. HNF4γ has yet to be paired with an endogenous ligand
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