- Open Access
Primate-specific evolution of an LDLR enhancer
- Qian-fei Wang†1, 2,
- Shyam Prabhakar†1, 2,
- Qianben Wang3,
- Alan M Moses1,
- Sumita Chanan1,
- Myles Brown3,
- Michael B Eisen1,
- Jan-Fang Cheng1, 2,
- Edward M Rubin1, 2Email author and
- Dario Boffelli1, 2
© Wang et al.; licensee BioMed Central Ltd. 2006
- Received: 11 May 2006
- Accepted: 2 August 2006
- Published: 2 August 2006
Sequence changes in regulatory regions have often been invoked to explain phenotypic divergence among species, but molecular examples of this have been difficult to obtain.
In this study we identified an anthropoid primate-specific sequence element that contributed to the regulatory evolution of the low-density lipoprotein receptor. Using a combination of close and distant species genomic sequence comparisons coupled with in vivo and in vitro studies, we found that a functional cholesterol-sensing sequence motif arose and was fixed within a pre-existing enhancer in the common ancestor of anthropoid primates.
Our study demonstrates one molecular mechanism by which ancestral mammalian regulatory elements can evolve to perform new functions in the primate lineage leading to human.
- Additional Data File
- Mouse Lemur
- Conservation Score
- Anthropoid Primate
- DNaseI Hypersensitive Site
Since King and Wilson's provocative paper was published in 1975 , differences in gene regulatory sequences have been predicted to be among the major sources of phenotypic evolution and divergence among animals. Consistent with this hypothesis, cis-regulatory changes have been found to play an important role in the evolution of morphologic features in model organisms . In contrast, evolution of physiology has been linked to changes in protein coding sequences, when studied in animal vision, digestive metabolism, and host defense [3–7]. The contribution of regulatory sequence changes to the evolution of physiologic differences, however, is largely unexplored [8, 9].
To examine the role of cis-regulatory changes in the emergence of novel physiologic traits in primates, we investigated the evolution of regulatory elements of the low-density lipoprotein (LDL) receptor gene (LDLR), which is a key player in maintaining lipid homeostasis. Cholesterol metabolism in humans has diverged in a variety of ways from that of many distant mammals such as rodents and dogs, with humans in general being more susceptible to diet-induced hypercholesterolemia . The pivotal role of LDLR in cholesterol metabolism, coupled with its known expression differences among mammals , makes it a prime candidate for investigating primate-specific evolution of regulatory sequences. Here, we present molecular data supporting the gain of a cholesterol-sensing DNA motif in an ancestral mammalian LDLR regulatory element at a specific stage in primate evolution.
Identification of primate-specific noncoding elements in the LDLRlocus
To confirm independently the lack of significant conservation of the PS1 and PS2 elements between human and distant mammals, we also analyzed human-mouse alignment using a sliding-window percentage identity conservation criterion. We found that the human-mouse percentage identities across PS1 and PS2 were below 50% (Figure 1 and data not shown). This is close to the background percentage identity in aligned intergenic DNA and is well below the threshold of 70% identity that is normally applied to the detection of conserved functional sequences . We further verified that the phastCons program  detects no conserved sequences overlapping PS1 and PS2 (data not shown). Although the phastCons predictions, obtained from the UCSC Genome Browser, are in general based on alignment of 17 mammalian and nonmammalian species, conservation scores in the LDLR locus reflect only mammalian conservation because more distant genomes exhibit very limited nonexonic alignment in this locus.
PS2 enhancer functional divergence correlates with sequence constraint
Conservation P value
Relative enhancer strength
4.8 × 10-5
The human LDLRPS2 element exhibits significantly greater enhancer activity than its mammalian orthologs
To explore the regulatory function, if any, of mammalian sequences orthologous to human PS2, we cloned the PS2-aligned sequences from lemur, mouse, and dog into the luciferase reporter vector described above and compared their activities with that of the human sequence. Despite the lack of statistically significant sequence constraint between the human enhancer and its lemur, mouse, and dog orthologs, the latter three sequences exhibited enhancer activity both in vitro and in vivo (Figure 2). The human regulatory element, however, consistently exhibited stronger enhancer activity in both assays, driving twofold greater expression than lemur or dog PS2 and fourfold greater expression than mouse (Figure 2a). This observation, coupled with the evidence of negative selection acting on the primate enhancer and the lack of significant sequence constraint between the anthropoid primate and mammalian PS2 sequences (conservation P value; Table 1), suggests that the stronger enhancer activity in human is a gain of function in the anthropoid primate lineage with a potentially important adaptive role in these species.
An anthropoid-primate specific sterol regulatory element contributes to distinct human PS2 enhancer activity
The functional role of the binding motif identified by computational analysis was explored by site-specific mutagenesis. A 4 bp substitution was introduced into the SRE, which was expected to inactivate the site completely based on a previously reported mutagenesis study . The 4 bp substitution in the SRE decreased human enhancer activity in the human cell culture assay and the in vivo mouse liver DNA transfer assay to a level comparable with that in lemur, mouse, and dog enhancers; these species lack a computationally predicted SRE (Figure 2). The functionality of the SRE, found exclusively in anthropoid primates, suggests that this element is likely to contribute to the stronger activity found in these species. We also identified within the 860 bp enhancer a 21 bp subregion that exhibits strong conservation across mammalian species including lemur, mouse lemur, galago, mouse and dog, and that contains predicted binding sites for transcription factors activating enhancer binding protein (AP)-4 and AP-1. Deletion of the conserved 21 bp sequence from either human or dog PS2 resulted in a significant reduction in enhancer activity (data not shown), suggesting that the evolutionarily conserved AP-4 and AP-1 sites are important for the core enhancer activity shared among mammals. It is worth noting that such short blocks of genuinely constrained sequence are not easily distinguishable from the numerous 'coincidentally conserved' sequence fragments that are likely to occur in large genomic regions as a consequence of stochastic variation in the incidence of neutral mutations. Incorporation of additional information, namely the binding specificities of transcription factors, was required to classify this 21 bp fragment as a functional candidate. Thus, conservation of this short subsequence in multiple mammals does not detract from the fact that the enhancer sequence is significantly conserved only in anthropoid primates, as described above.
We have shown phylogenetic and molecular data supporting the evolution of differential gene expression of LDLR in mammals. Transcriptional control of LDLR is mainly effected through the intracellular cholesterol sensor SREBP-2. The latter was previously shown to mediate the increased transcription of LDLR in response to low cholesterol levels through an SRE in the LDLR promoter [23, 30], which is conserved in all mammals examined. The additional SRE found in the PS2 enhancer in primates may lead to differential response to SREBP-2 among mammals. Although the contribution of the PS2 enhancer to the in vivo regulation of LDLR remains to be elucidated, these results suggest that species-specific regulation of LDLR is expected in conditions that result in decreased intracellular cholesterol levels, such as reduced availability of dietary cholesterol, and has implications for the study of LDLR response to cholesterol-lowering drugs in animal models.
Although the human LDLR coding sequence and promoter are well conserved in all sequenced mammals (Figure 1 and Additional data file 1), our data support the modification of the expression characteristics of this gene through the primate-specific evolution of a distal regulatory element. We have shown the emergence and fixation of a SRE in the common ancestor of anthropoid primates, which modifies the expression driven by a pre-existing mammalian enhancer shared by all tested mammals. This demonstrates one mechanism by which mammalian regulatory elements can evolve to perform new functions. Given the vital importance of LDLR in energy storage, the appearance of a new cholesterol sensing element in the LDLR enhancer might have played a role in the evolution of new physiologic features, because the ancestor of anthropoid primates adapted to different metabolic requirements and diets.
The human LDLR promoter was cloned in the proper orientation upstream of the luciferase cDNA in the pGL3Basic construct (Promega, Madison, WI, USA). The human PS1 element and the PS2 elements from human, lemur, mouse, and dog LDLR loci were polymerase chain reaction (PCR) cloned into poly-linker sites in the (-) orientation upstream of the promoter. The cloned human PS1 element corresponds to the Gumby predicted conserved sequence and approximately 200 bp of flanking sequence on either side (hg18, chr19:11067913-11068639). To clone the human PS2 element, the region containing human PS2 was PCR cloned into pGL3Basic (see Additional data file 4 for primer sequences), and digested with SpeI and NheI to only include the Gumby predicted conserved sequence and approximately 200 bp of flanking sequence on either side (hg18, chr19:11110333-11111194). Site-specific point mutations and deletions were introduced into human and dog PS2 elements using QuikChangeII site-directed mutagenesis kit (Stratagene, La Jolla, CA, USA), in accordance with the manufacturer's protocol and were confirmed by sequencing. The expression construct for human mature form of SREBP-2 (pcDNA.2FLAG SREBP-2) was kindly provided by Dr Timothy F Osborne (UC Irvine). The human LDLR promoter (hg18, chr19:11060880-11061099) was PCR amplified (see Additional data file 4 for primers used).
Transient transfection reporter assay
Cells of human embryonic kidney cell line 293T (ATCC CRL-11268) were grown at 37°C and 5% carbon dioxide CO2 in Dulbecco's modified Eagle's medium (ATCC), supplemented with 10% fetal bovine serum (Hyclone, Logan, UT, USA), l-glutamine, and penicillin-streptomycin. Cells with a passage number below 15 were used. The cells were grown in 12-well plates (4 × 104 cells/well) and transfected using Fugene (Roche Molecular Biochemicals, Indianapolis, IN, USA), in accordance with the manufacturer's protocol. Briefly, 100 ng of each assayed plasmid and 10 ng pCMVβ (BD Biosciences, Franklin Lakes, NJ, USA) were mixed with 1.5 μl Fugene and added to each well. Following 42-48 hours of incubation, cells were harvested and lysed. Activity of luciferase and β-galactosidase was measured using the Luciferase Assay System (Promega) and the Galacto-Light Plus (Applied Biosystems, Foster City, CA, USA), respectively. Luciferase activity for each sample was normalized to the β-galactosidase assay control. For co-transfection experiments, 100 ng of the lulciferase reporter gene construct, 3 ng of SREBP-2 expression vector, and 10 ng of pCMVβ were used. Transfections were carried out in duplicate. All experiments are representative of at least three independent transfections.
Tail vein plasmid DNA transfer assays
Tail vein injection was performed as described by Herweijer and Wolff , following the TransIT® In Vivo Gene Delivery System (Mirus Corporation, Madison, WI, USA) protocol. Six to nine FVB male mice (Charles River Laboratory, Wilmington, MA, USA) at age 7-8 weeks were used for each reporter gene construct. Ten micrograms of each reporter construct, along with 2 μg of pCMVβ (BD Biosciences) to correct for delivery efficiency, were injected into each mouse. The entire content of the syringe was delivered in 3-5 s. Animals were killed 24 hours later, livers extracted, measured to correct for size, homogenized, and centrifuged for 15 min at 4°C, 14,000 rpm. Activities of luciferase and β-galactosidase were measured as described above. All P values are from the two-sample Wilcoxon rank-sum (Mann-Whitney) test using STATA (STATA Corporation, College Station, TX, USA). All experimental results are representative of two independent plasmid DNA transfer assays.
HepG2 cells (ATCC HB-8065) were cultured in DMSF (defined medium serum free) medium for 24 hours for induction of endogenous SREBPs . Chromatin immunoprecipitaion assays were performed as described previously . Cross-linked chromatin was immunoprecipitated with a specific SREBP-2 antibody (Santa Cruz sc-8151)  or IgG control.
Sources of sequence data
Draft sequences of baboon, colobus, dusky titi, marmoset, owl monkey, lemur, and galago bacterial artificial chromosomes (BACs) were determined by sequencing ends of 3 kb subclones to 8- to 10-fold coverage using BigDye terminators (Applied Biosystems) and assembling reads into contigs with the Phred-Phrap-Consed suite, as described previously . All BAC sequences were submitted to GenBank with the following species and accession numbers: baboon (Papio hamadryas), AC140974; colobus (Colobus guereza), AC150433; marmoset (Callithrix jacchus), AC145530; dusky titi (Callicebus moloch), AC144655; owl monkey (Aotus hybrid), AC171393; squirrel monkey (Saimiri boliviensis boliviensis), AC146467; lemur (lemur catta), AC118569; mouse lemur (microcebus murinus), AC175656; and galago (otolemur garnetti), AC175655). Human, chimpanzee, rhesus, mouse, rat, and dog sequences were downloaded from the UCSC Genome Bioinformatics website .
Analysis of sequence conservation
We aligned the human LDLR locus (chr19:11,055,219-11,117,169; NCBI Build 35) to its orthologs in baboon, colobus, dusky titi, marmoset, owl monkey, lemur, mouse, and dog using MLAGAN . Because incomplete primate sequence availability, we included only about 6 kb of the 5' intergenic region in the analysis. Aligned sequences were scanned for statistically significant evolutionarily conserved regions using Gumby [12–14]. Gumby goes through the following three-step process to identify statistically significant conservation in the global alignment input. First, noncoding regions in the alignment are used to estimate the local neutral mismatch rates among all pairs of aligned sequences. The rates are used to derive a log-likelihood scoring scheme for slow versus neutral evolution, in which the slow rate is set to some fraction (in this case, half) of the neutral rate. Second, each alignment position is then assigned a conservation score using a phylogenetically weighted sum-of-pairs scheme. Third, conserved regions of any length are identified as alignment blocks with a high cumulative conservation score and assigned P values using Karlin-Altschul statistics . We set a threshold P value of 0.1 in a baseline human sequence length of 10 kb. Conserved regions identified by Gumby were visualized using RankVISTA. In addition, human-mouse sequence conservation was analyzed using the VISTA web server [37, 38], with the standard criterion of 70% sequence identity in window of size 100 bp.
Binding site prediction
We scanned the aligned enhancer sequences for predicted transcription factor binding sites using DiAlign TF . Anthropoid primate (human, baboon, colobus, dusky titi, marmoset, and owl monkey) sequences were assessed for the presence of sites conserved across all six species that were predicted to bind one of the following liver-expressed transcription factors: C/EBP (CCAAT/enhancer-binding protein), LXR (liver X receptor), FXR (farnesoid X receptor), COUP-TF (Chicken Ovalbumin Upstream Promoter Transcription Factor), peroxisome proliferator-activated receptor (PPAR), HNF1 (hepatocyte nuclear factor 1), HNF3, HNF4, and SREBP. Binding sites common to primates and mammals were predicted on the basis of conservation of any vertebrate transcription factor motif in at least eight of the 10 analyzed species (six anthropoid primates, lemur, mouse, rat, and dog). Motif scores of the SREs or SRE orthologs of individual species were calculated using rVISTA  and normalized so that the maximum achievable score is 1.0, and the expected score of a random nucleotide sequence with the local GC content is zero. The score distribution of functional SREs was calculated from the binding profile of SREBP , assuming that nucleotide frequencies at each position in the motif are independent. We retrospectively augmented the species set with SRE orthologs from chimpanzee, rhesus, squirrel monkey, mouse lemur and galago, based on pair-wise alignments of those species to human.
The following additional data are available with the online version of this paper: A figure showing the conservation profiles of the LDLR locus using (A) human-dog and (B) human-lemur sequence comparisons (Additional data file 1); a figure showing the DNaseI hypersensitive site mapping around the LDLR PS2 region in human liver cell line HepG2 (Additional data file 2); a figure showing that human LDLR PS2 enhancer activity is independent of the LDLR promoter (Additional data file 3); a table listing the primers used in the cloning of human LDLR promoter and PS2 elements from indicated species (Additional data file 4); and a table listing the primers used in ChIP assay (Additional data file 5).
We thank J Noonan, L Pennacchio, A Visel, S Tringe, N Ahituv, and other Rubin laboratory members for suggestions and criticisms on the manuscript, and Tim Osborne for providing the SREBP-2 expression vector. B Kullgren and S Phouanenavong provided technical assistance for tail vein plasmid DNA transfer assay.
Research was conducted at the EO Lawrence Berkeley National Laboratory and at the Joint Genome Institute. This work was supported by the Director, Office of Science, of the US Department of Energy under Contract No. DE-AC02-05CH11231 and NIH-NHLBI grant numbers THL007279F and U1HL66681B.
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