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- Table of Contents
International Journal of Genomics
Volume 2013 (2013), Article ID 387594, 9 pages
A New Exon Derived from a Mammalian Apparent LTR Retrotransposon of the SUPT16H Gene
1Department of Biological Sciences, College of Natural Sciences, Pusan National University, Busan 609-735, Republic of Korea
2Department of Nanobiomedical Science & WCU Research Center, Dankook University, Cheonan 330-714, Republic of Korea
Received 15 November 2012; Accepted 12 February 2013
Academic Editor: Soraya E. Gutierrez
Copyright © 2013 Min-In Bae et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
The SUPT16H gene known as FACTP140 is required for the transcription of other genes. For transcription, genes need to be complexed with accessory factors, including transcription factors and RNA polymerase II. One such factor, FACT, interacts with histones H2A/H2B for nucleosome disassembly and transcription elongation. The SUPT16H gene has a transcript and many expressed sequence tags (ESTs). We were especially interested in an MaLR-derived transcript (EST, BX333035) that included a new exon introduced by a transposable element, a mammalian apparent LTR retrotransposon (MaLR). The MaLR was detected ranging from humans to galagos, indicating the MaLR in the SUPT16H gene is integrated into the primate ancestor genome. A new exon was created by alternative donor site provided by the MaLR. The original transcript and the MaLR-derived transcript were expressed in various human, rhesus monkey, and other primate tissues. Additionally, we identified a new alternative transcript that included the MaLR, but there was no significant difference in the expression of the original transcript and the MaLR-derived transcript. Interestingly, the new alternative transcript and the MaLR-derived transcript had the MaLR sequence in the new exon, but they had different structures by adopting different splice sites. From this study, we verified transposable elements that contributed to transcriptome diversity.
Transposable elements (TEs) dispersed in the mammalian genome are on the rise, as completion of the whole human genome sequence. Contrary to our expectations, TEs, thought to be “junk DNA,” were estimated to account for approximately 45% of the human genome (International Human Genome Sequencing Consortium, 2001). TEs can be categorized by various features such as the capacity to mobilize themselves, DNA/RNA intermediation, and the existence of a long terminal repeat (LTR). Endogenous retroviruses (ERVs) and long interspersed elements (LINEs) have gene-encoding enzymatic machinery that could mobilize to other genomic regions as autonomous elements. However, nonautonomous elements, especially Alu elements, which are classified as short interspersed elements (SINE) and SINE-variable number tandem repeat-Alu-like sequences (SVA), mobilize using the reverse transcriptase of the LINE. All of the TEs described above are integrated into the host genome by their RNAs, but the integration of DNA transposons is mediated by DNA. These groups can be restructured by the existence of LTRs on both ends. ERVs and LTR retrotransposons have LTRs, but SINEs and LINEs are non-LTR elements [1–3].
One group of retrotransposon-like elements, mammalian apparent LTR retrotransposons (MaLRs), accounts for approximately 3.65% and 4.82%, including solitary LTRs, of the human and mouse genome, respectively . The structure of MaLRs is similar to that of ERVs with LTRs. However, MaLRs can be distinguished from other retroviruses by some differences. Typical ERVs consist of an internal region, gag, pol, and env with LTRs on both sides. LTRs are very important for integration and transcription because they function as a promoter element, transcription start site, and polyadenylation signal and site . Compared to ERVs, MaLRs have short internal sequences and LTRs at the 5′ and 3′ ends, but they do not have a transcription initiation site, reverse transcriptase, and primer binding site . Recent studies have shown that TEs contributed to primate genome evolution through gene structure variation and regulation by integrating into an intron, gene-flanking region, and an exon [7, 8]. Additionally, TEs that integrate into introns could make alternative exons or cassette exons in a process termed “exonization” within human and mouse protein-coding genes ; in contrast, TEs can make new introns in a process called “intronization.” These events could help with the understanding of transcriptome and proteome complexities [9–11]. The exonization of the primate-specific Alu element is well established in the divergence of human and chimpanzee genomes as a major mechanism of exon creation [12, 13]. Lev-Maor et al. (2003) reported that the Alu consensus sequence could provide a splice site, leading to exonization . In the case of LTRs, Piriyapongsa et al. (2007) reported that 256 of 1057 LTR retrotransposons related to human genes were observed in protein-coding regions, and 50 protein-coding exons of 45 genes were derived wholly from LTR retrotransposons. Furthermore, they analyzed alternative exons of the interleukin 22 receptor, the alpha 2 gene (IL22RA2), which was derived from MaLRs that provided splice sites, indicating the important roles of TEs in human evolution; this result coincided with those of previous studies [1, 5]. Importantly, these structural variations of genes are associated with gene regulation and genetic disease .
Here, we identified a transcript that included an MaLR in the SUPT16H gene. The SUPT16H gene, also known as FACTP140, is a component of the facilitates chromatin transcription (FACT) complex. In eukaryotic cells, the transcription of genes requires RNA polymerase II and transcription factors with altered chromatin structure . In order to initiate transcription, DNA needs to be in an open structure that is moderated by the alteration of chromatin with accessory factors, facilitating access to the DNA. FACT specifically interacts with histones H2A/H2B to affect nucleosome disassembly and transcription elongation . As described above, the SUPT16H gene has an original transcript consisting of 26 exons. However, the integration of an MaLR created a new exon that was expressed transcriptionally (BX333035). Furthermore, we found a new alternative transcript, including the MaLR-derived exon. We assumed the time of integration of the MaLR into the genome by PCR amplification. All of the primates assayed had the MaLR in the SUPT16H gene, which was a natural result of its conservation in the mammalian genome. Additionally, we compared the structure and expression of 2 transcripts, including MaLR. The expression patterns of the 2 transcripts in several tissues of humans, crab-eating monkey, marmoset, and squirrel monkey were ubiquitous with no significant tissue specificity or species specificity. Structurally, the 2 transcripts included the exon-derived MaLR, but they adopted different splice sites, leading to exons of different sizes. Taken together, we showed that the MaLR could regulate gene expression at the transcriptional level, that is, TEs could provide transcriptome diversity, resulting in the proteome’s capacity for diversification, which potentially occupies an important role in the host genome.
2. Materials and Methods
2.1. Computational Analysis
To identify the sequences related to the MaLR, we scanned the human reference genome sequence, human ESTs, and human RefSeq mRNAs. Using the MaLR consensus sequence as a query, we screened nonredundant databases through BLAST version 2.2.26+ to identify the novel hybrid transcripts of the MaLR and SUPT16H . Then, we aligned the transcripts of the SUPT16H gene to identify the precise splicing patterns. TEs included in the SUPT16H transcripts and their genomic loci were identified using the RepeatMasker program (http://www.repeatmasker.org/), referencing a library containing the consensus sequences from Repbase Update . Using the EST and RefSeq mRNAs, we accurately reconstructed the SUPT16H gene structure. To analyze the sequences of the various SUPT16H transcripts, we aligned them using the ClustalW program .
2.2. Preparing for DNA and RNA
Using the TRIzol reagent (Invitrogen), we extracted the total RNA from the cerebrum, cerebellum, pituitary gland, heart, lung, spleen, liver, pancreas, kidney, and urinary bladder of the crab-eating monkey; the heart, lung, brain, stomach, liver, kidney, pancreas, colon, spleen, and small intestine of the marmoset; and the heart, esophagus, diencephalon, small intestine, lung, pancreas, cerebrum, colon, and stomach of the squirrel monkey. The total RNA from human tissues, including the adrenal gland, cerebellum, whole brain, heart, kidney, liver, lung, testis, trachea, bone marrow, fetal brain, fetal liver, placenta, prostate, salivary gland, skeletal muscle, spinal cord, thymus, thyroid, and uterus, were purchased from Clontech. We isolated the mRNA from the total RNA by using PolyATract mRNA Isolation Systems (Promega).
We used the genomic DNA of the following species: (1) hominoids: common chimpanzee (Pan troglodytes), gorilla (Gorilla gorilla), orangutan (Pongo pygmaeus), and gibbon (Hylobates agilis); (2) Old World monkeys: Japanese monkey (Macaca fuscata), rhesus macaque (M. mulatta), bonnet macaque (M. radiata), mandrill (Mandrillus sphinx), mangabey (Cercocebus agilis), African green monkey (Chlorocebus aethiops), colobus (Colobus guereza), and langur (Trachypithecus cristatus); (3) New World monkeys: night monkey (Aotus trivirgatus), squirrel monkey (Saimiri sciureus), and common marmoset (Callithrix jacchus); and (4) prosimian: ring-tailed lemur (Lemur catta) and a galago (Otolemur crassicaudatus). These genomic DNA were isolated from the heparinized blood samples according to a standard protocol . After anticoagulant, the buffy coat was isolated carefully. And then, proteinase K and phenol equilibrated with Tris-Cl were treated for extraction. The viscous aqueous was transferred and ammonium acetate and ethanol were added to form a precipitate. Lastly, the DNA precipitate was washed, dried, and dissolved in TE (Tris and EDTA). Dr. Takenaka (Primate Research Institute, Kyoto University) kindly provided genomic DNA of primates after conducting this procedure.
2.3. PCR and Reverse Transcription (RT)-PCR Amplification
Using the genomic DNA of humans and 17 primates, the MaLR in the SUPT16H gene was amplified to analyze the integration time in the primate genome. The primer pair included GS1 (5′-AATTGGCGGAAAGGAGAAG-3′) and GAS2 (5′-GAGGCAGTCATTCCAGCTCT-3′).
SUPT16H transcripts were analyzed by RT-PCR amplification. M-MLV reverse transcriptase (Promega) with an annealing temperature of 42°C and an RNase inhibitor (Promega) were used for the reverse transcriptions of the transcripts. The SUPT16H transcripts were amplified with a primer pair from GenBank (accession number NM001033560) consisting of S1 (5′-AATTGGCGGAAAGGAGAAG-3′) and AS1 (5′-GAGGCAGTCATTCCAGCTCT-3′). The SUPT16H transcripts related to the MaLR were amplified with a primer pair from GenBank (BX_333035) consisting of S2 (5′-TCCAGTTCTCTGTTCTGCCA-3′) and AS2 (5′-TGTGTGGAGCTTCAAGCAAG-3′). The PCR samples were subjected to an initial denaturation step of 4 min at 94°C, followed by 30 cycles of PCR at 40 s of denaturation at 95°C, 40 s of annealing at 55°C, and 90 s of extension at 72°C, followed by a final extension step of 7 min at 72°C. As a standard control, GAPDH was amplified with a primer pair consisting of GPH-S (5′-GAGCCCCAGCCTTCTCCATG-3′) and GPH-AS (5′-GAAATCCCATCACCATCTTCCAGG-3′) from human GAPDH (GenBank accession number NM002046).
3. Results and Discussion
3.1. Structure of the SUPT16H Gene with the Integration of a Transposable Element
The SUPT16H gene located on chromosome 14q11.2 encodes accessory factors that may facilitate access to DNA by unpackaging the chromatin structure. It contains 26 exons with several transposable elements such as MaLRs (LTR), Alus (SINE), and L1s (LINE) distributed in the intronic regions. The SUPT16H transcript related to the MaLR (MaLR-derived transcript) has 3 exons, and its last exon was created by the integration of the MaLR LTR element in the opposite direction of the host gene (Figure 1).
MaLRs are considered to function in the mammalian genome by providing alternative splice sites, promoters, and other cis-regulatory elements, similar to other TEs that have been conserved during primate evolution . For example, RNF19 has an alternative transcript resulting from the exonization of MaLR and AluJo. Specifically, the MaLR in the first exon has promoter activity in the sense orientation in the African green monkey fibroblast cell line, Cos7, and the human colorectal carcinoma cell line, HCT116 . As described above, MaLRs are known to be present in genomes of rodents to primates and humans, indicating that they were distributed before the divergence of eutherian mammals. In order to compare the integration time of the MaLR in the SUPT16H gene with that from previous reports, we conducted PCR amplification using the genomic DNA of human and other primates (Figure 2). We identified an amplicon that was 481 bp long in all of the primates that we assessed, indicating that the MaLR in the SUPT16H gene integrated into the genome of a common ancestor before the divergence of the New World monkey and prosimians. In addition, from the sequencing alignment, we also identified 40 bp and 4 bp of specific sequences in Japanese macaque (Figure 2(b)). These sequences were not detected in any other primate, including the rhesus macaque, which belongs to the Old World monkey family. Thus, these distinct sequences distinguish the Japanese macaque from other primates.
3.2. Expressional Analysis of RefSeq mRNA and EST BX333035 of the SUPT16H Gene
TEs distributed in the mammalian genome have played important roles in gene regulation and evolution . One of the typical characteristics of TEs which is that they affect the transcription of cellular genes by exonization, which creates an alternatively spliced exon by integration into exonic or intronic regions, has been reported in many studies [24, 25]. Actually, these alternative transcripts are transient and flexible according to the cellular environment and stimuli. However, alternatively spliced variants can be stabilized and increased without selection, and exonization can lead to not only transcriptome diversity but also proteome diversity [2, 10]. Furthermore, these events occur differently or specifically according to the tissue, developmental stage, and disease; thus, alternative transcripts are used to mine disease diagnostic markers [9, 26].
To confirm whether the MaLR sequences are expressed and could regulate transcription, we conducted RT-PCR analysis of the RefSeq mRNA (original transcript) and MaLR-derived transcript (BX333035) from several human tissues. Firstly, original transcript was expressed broadly in human tissues. It did not show strong expression or specific expression in particular tissues. We analyzed its expression in tissues of other primates, including the crab-eating monkey, common marmoset, and squirrel monkey (Figure 3). Like the expression in humans, it was ubiquitously expressed in the tissues of these primates. Because we identified japanese monkey-specific sequences, we conducted RT-PCR analysis in rhesus macaque samples to compare the expression in Old World monkeys. However, we could not detect a difference in the SUPT16H expression between the japanese monkey and rhesus macaque (data not shown).
Gene expression is a process that produces RNA or proteins through transcription, splicing, and translation. The initiation of gene expression was regulated by chromatin structure. The SUPT16H gene is a subunit of the FACT complex that acts as a chromatin-specific transcription elongation factor and interacts with histone H2A/H2B to disassemble nucleosomes and promote transcription elongation . Namely, the broad expression of SUPT16H in human and other primate tissues indicated its essential function for gene expression. Next, we analyzed the expression of MaLR-derived transcript. As shown in Figure 4, a transcript related to the MaLR was also expressed broadly in human tissues. This product was also detected in tissues of crab-eating monkey, common marmoset, and squirrel monkey. There was hardly any difference in the expression of 2 transcripts which indicated MaLR did not affect the expression of the SUPT16H gene.
3.3. Identification of an Alternative Transcript and Its Creation
From the RT-PCR analysis, we identified a new alternative transcript. Its product was longer than that of the original transcript because alternative splicing retained an intronic region. This intronic region was derived from the MaLR. The MaLR in the intron was not spliced and exonized (exon 2′) wholly between exons 2 and 3 (Figure 3). Comparing the new alternative transcript and the MaLR-derived transcript (BX_333035), we identified specific features of alternative splicing. Entire sequences of the new exon of the alternative transcript identified in RT-PCR were derived from the MaLR. In addition, this exon was not created by canonical splicing sites. As shown in Figure 5, the MaLR provided both typical alternative splice sites, the acceptor site (AG) and a nucleotide (G) of the donor site (GT). Although these splicing sites were typical sequences recognized by the spliceosome, the splicing pattern could be changed. In case of the transcript related to the MaLR (BX_333035), the MaLR in the intronic region was also exonized to form a new alternative transcript. Strangely, the pattern of splicing was different. Only 1 site, the acceptor site, was recognized by the spliceosome, and the donor site was skipped. Thus, the new exon was elongated. Additionally, the elongated exon included MaLR-derived sequences and sequences of intron and exon 3 of the original and new alternative transcript. In spite of the different splicing pattern, the new alternative transcript was expressed broadly in tissues of humans and other primates, similar to the original and MaLR-related transcripts (Figures 3 and 4).
Alternative splicing is a common mechanism by which most genes are processed [27, 28]. In a previous report, approximately 60% of human genes have at least one alternative transcript . Alternative splicing can be controlled by genetic mutation and epigenetic alteration [30, 31]. Generally, AG and GT are recognized by the spliceosome as the splicing site. However, the spliceosome can recognize splicing sites created by mutation and cryptic splicing sites, leading to alternative splicing . In addition to point mutations, the integration of transposable elements can induce alternative splicing as genetic mutations [2, 25]. If the 2 transcripts showed different and tissue-specific expression patterns, we could assume that tissue-specific factors contributed to alternative splicing; however, both transcripts were expressed broadly in tissues of humans and primates . Alternatively, we could guess that the chromatin structure affected alternative splicing. The mechanism of recognizing splice sites can be altered by epigenetic regulation . Various mechanisms can be considered to understand the differences between the 2 transcripts. Compared to original transcript, the new exon is very unstable and temporary. First, we could expect this new exon was created by cryptic splicing site. However, the new exon includes intronic sequences by the typical splice site, AG-GT (3′–5′), in the new alternative transcript, and AG (3′) in the MaLR-derived transcript existing in the intron. If so, we could guess that the acceptor site and donor site of the new exon could be marked as a weak splice site by epigenetic regulation, such as histone modifications and DNA methylationan, although it was the typical splice site. In a previous study, histone modification was reported as important factor for alternative splicing. Among histone modifications such as H3K36me3, H3K79me1, H2BK5me1, H3K27me1, H3K27me2, and H3K27me3 enriched in exon, the donor site of the new exon could be recognized weakly by the spliceosome with H3K36me3 which is found in weakly expressed exon [35, 36]. Additionally, the DNA methylation and the CG content in the new exonic region could affect the expression of the 2 transcripts. Zhou et al. (2012) reported that exclusive exons have lower levels of CG and methylated CG, whereas retained intron has higher levels .
We suggest that the MaLR integrated into an intron of the SUPT16H gene before the divergence of New World monkeys and prosimians, and it played a biological role in the evolution of the SUPT16H gene during primate evolution by providing an alternative splice site. Although further analyses are required to conclusively elucidate the functions of the transcriptional variants of the SUPT16H gene in primate genomes, the results of this study will help us understand the characteristics of the transposable element insertion driving the transcript diversification and its effect on the evolution of the host gene.
M. I. Bae and Y. J. Kim contributed equally to this work.
All the authors contributed to this study and declared that no conflict of interests exists. This research was supported by the Bio-Scientific Research Grant funded by the Pusan National University (PNU-2008-101-20080596000).
- H. L. Levin and J. V. Moran, “Dynamic interactions between transposable elements and their hosts,” Nature Reviews Genetics, vol. 12, no. 9, pp. 615–627, 2011.
- J. Schmitz and J. Brosius, “Exonization of transposed elements: a challenge and opportunity for evolution,” Biochimie, vol. 93, no. 11, pp. 1928–1934, 2011.
- J. Lee, J. Ha, S.-Y. Son, and K. Han, “Human genomic deletions generated by SVA-associated events,” Comparative and Functional Genomics, vol. 2012, Article ID 807270, 7 pages, 2012.
- P. K. Mandal and H. H. Kazazian Jr., “SnapShot: vertebrate transposons,” Cell, vol. 135, no. 1, pp. 192–192.e1, 2008.
- J. Piriyapongsa, N. Polavarapu, M. Borodovsky, and J. McDonald, “Exonization of the LTR transposable elements in human genome,” BMC Genomics, vol. 8, article 291, 2007.
- A. F. A. Smit, “Identification of a new, abundant superfamily of mammalian LTR-transposons,” Nucleic Acids Research, vol. 21, no. 8, pp. 1863–1872, 1993.
- R. E. Mills, E. A. Bennett, R. C. Iskow et al., “Recently mobilized transposons in the human and chimpanzee genomes,” American Journal of Human Genetics, vol. 78, no. 4, pp. 671–679, 2006.
- R. Cordaux and M. A. Batzer, “The impact of retrotransposons on human genome evolution,” Nature Reviews Genetics, vol. 10, no. 10, pp. 691–703, 2009.
- N. Sela, B. Mersch, A. Hotz-Wagenblatt, and G. Ast, “Characteristics of transposable element exonization within human and mouse,” PLoS ONE, vol. 5, no. 6, Article ID e10907, 2010.
- R. Sorek, “The birth of new exons: mechanisms and evolutionary consequences,” RNA, vol. 13, no. 10, pp. 1603–1608, 2007.
- N. Sela, B. Mersch, N. Gal-Mark, G. Lev-Maor, A. Hotz-Wagenblatt, and G. Ast, “Comparative analysis of transposed element insertion within human and mouse genomes reveals Alu's unique role in shaping the human transcriptome,” Genome Biology, vol. 8, no. 6, article R127, 2007.
- L. Lin, S. Shen, A. Tye et al., “Diverse splicing patterns of exonized Alu elements in human tissues,” PLoS Genetics, vol. 4, no. 10, Article ID e1000225, 2008.
- S. Shen, L. Lin, J. J. Cai et al., “Widespread establishment and regulatory impact of Alu exons in human genes,” Proceedings of the National Academy of Sciences of the United States of America, vol. 108, no. 7, pp. 2837–2842, 2011.
- G. Lev-Maor, R. Sorek, N. Shomron, and G. Ast, “The birth of an alternatively spliced exon: 3′ splice-site selection in Alu exons,” Science, vol. 300, no. 5623, pp. 1288–1291, 2003.
- J. L. Goodier and H. H. Kazazian Jr., “Retrotransposons revisited: the restraint and rehabilitation of parasites,” Cell, vol. 135, no. 1, pp. 23–35, 2008.
- R. Belotserkovskaya, S. Oh, V. A. Bondarenko, G. Orphanides, V. M. Studitsky, and D. Reinberg, “FACT facilitates transcription-dependent nucleosome alteration,” Science, vol. 301, no. 5636, pp. 1090–1093, 2003.
- G. Orphanides, W. H. Wu, W. S. Lane, M. Hampsey, and D. Reinberg, “The chromatin-specific transcription elongation factor FACT comprises human SPT16 and SSRP1 proteins,” Nature, vol. 400, no. 6741, pp. 284–288, 1999.
- S. F. Altschul, T. L. Madden, A. A. Schäffer et al., “Gapped BLAST and PSI-BLAST: a new generation of protein database search programs,” Nucleic Acids Research, vol. 25, no. 17, pp. 3389–3402, 1997.
- J. Jurka, “Repbase Update: a database and an electronic journal of repetitive elements,” Trends in Genetics, vol. 16, no. 9, pp. 418–420, 2000.
- J. D. Thompson, D. G. Higgins, and T. J. Gibson, “CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice,” Nucleic Acids Research, vol. 22, no. 22, pp. 4673–4680, 1994.
- J. Sambrook, E. F. Fritsch, and T. Maniatis, Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, New York, NY, USA, 1989.
- J.-W. Huh, D.-S. Kim, H.-S. Ha et al., “Cooperative exonization of MaLR and AluJo elements contributed an alternative promoter and novel splice variants of RNF19,” Gene, vol. 424, no. 1-2, pp. 63–70, 2008.
- M. Warnefors, V. Pereira, and A. Eyre-Walker, “Transposable elements: insertion pattern and impact on gene expression evolution in hominids,” Molecular Biology and Evolution, vol. 27, no. 8, pp. 1955–1962, 2010.
- N. J. Bowen and I. K. Jordan, “Exaptation of protein coding sequences from transposable elements,” Genome Dynamics, vol. 3, pp. 147–162, 2007.
- I. Vorechovsky, “Transposable elements in disease-associated cryptic exons,” Human Genetics, vol. 127, no. 2, pp. 135–154, 2010.
- Q. Yi and L. Tang, “Alternative spliced variants as biomarkers of colorectal cancer,” Current Drug Metabolism, vol. 12, no. 10, pp. 966–974, 2011.
- E. T. Wang, R. Sandberg, S. Luo et al., “Alternative isoform regulation in human tissue transcriptomes,” Nature, vol. 456, no. 7221, pp. 470–476, 2008.
- Q. Pan, O. Shai, L. J. Lee, B. J. Frey, and B. J. Blencowe, “Deep surveying of alternative splicing complexity in the human transcriptome by high-throughput sequencing,” Nature Genetics, vol. 40, no. 12, pp. 1413–1415, 2008.
- D. L. Black, “Mechanisms of alternative pre-messenger RNA splicing,” Annual Review of Biochemistry, vol. 72, pp. 291–336, 2003.
- J. P. Venables, “Aberrant and alternative splicing in cancer,” Cancer Research, vol. 64, no. 21, pp. 7647–7654, 2004.
- Y. Zhou, Y. Lu, and W. Tian, “Epigenetic features are significantly associated with alternative splicing,” BMC Genomics, vol. 13, p. 123, 2012.
- M. Burset, I. A. Seledtsov, and V. V. Solovyev, “Analysis of canonical and non-canonical splice sites in mammalian genomes,” Nucleic Acids Research, vol. 28, no. 21, pp. 4364–4375, 2000.
- T. W. Nilsen and B. R. Graveley, “Expansion of the eukaryotic proteome by alternative splicing,” Nature, vol. 463, no. 7280, pp. 457–463, 2010.
- R. F. Luco, M. Allo, I. E. Schor, A. R. Kornblihtt, and T. Misteli, “Epigenetics in alternative pre-mRNA splicing,” Cell, vol. 144, no. 1, pp. 16–26, 2011.
- P. Kolasinska-Zwierz, T. Down, I. Latorre, T. Liu, X. S. Liu, and J. Ahringer, “Differential chromatin marking of introns and expressed exons by H3K36me3,” Nature Genetics, vol. 41, no. 3, pp. 376–381, 2009.
- R. Andersson, S. Enroth, A. Rada-Iglesias, C. Wadelius, and J. Komorowski, “Nucleosomes are well positioned in exons and carry characteristic histone modifications,” Genome Research, vol. 19, no. 10, pp. 1732–1741, 2009.