Evolution of the myosin heavy chain gene MYH14 and its intronic microRNA miR-499: muscle-specific miR-499 expression persists in the absence of the ancestral host gene
- Sharmin Siddique Bhuiyan†1,
- Shigeharu Kinoshita†1Email author,
- Chaninya Wongwarangkana1,
- Md Asaduzzaman1,
- Shuichi Asakawa1 and
- Shugo Watabe1, 2
© Bhuiyan et al.; licensee BioMed Central Ltd. 2013
Received: 27 November 2012
Accepted: 13 June 2013
Published: 6 July 2013
A novel sarcomeric myosin heavy chain gene, MYH14, was identified following the completion of the human genome project. MYH14 contains an intronic microRNA, miR-499, which is expressed in a slow/cardiac muscle specific manner along with its host gene; it plays a key role in muscle fiber-type specification in mammals. Interestingly, teleost fish genomes contain multiple MYH14 and miR-499 paralogs. However, the evolutionary history of MYH14 and miR-499 has not been studied in detail. In the present study, we identified MYH14/miR-499 loci on various teleost fish genomes and examined their evolutionary history by sequence and expression analyses.
Synteny and phylogenetic analyses depict the evolutionary history of MYH14/miR-499 loci where teleost specific duplication and several subsequent rounds of species-specific gene loss events took place. Interestingly, miR-499 was not located in the MYH14 introns of certain teleost fish. An MYH14 paralog, lacking miR-499, exhibited an accelerated rate of evolution compared with those containing miR-499, suggesting a putative functional relationship between MYH14 and miR-499. In medaka, Oryzias latipes, miR-499 is present where MYH14 is completely absent in the genome. Furthermore, by using in situ hybridization and small RNA sequencing, miR-499 was expressed in the notochord at the medaka embryonic stage and slow/cardiac muscle at the larval and adult stages. Comparing the flanking sequences of MYH14/miR-499 loci between torafugu Takifugu rubripes, zebrafish Danio rerio, and medaka revealed some highly conserved regions, suggesting that cis-regulatory elements have been functionally conserved in medaka miR-499 despite the loss of its host gene.
This study reveals the evolutionary history of the MYH14/miRNA-499 locus in teleost fish, indicating divergent distribution and expression of MYH14 and miR-499 genes in different teleost fish lineages. We also found that medaka miR-499 was even expressed in the absence of its host gene. To our knowledge, this is the first report that shows the conversion of intronic into non-intronic miRNA during the evolution of a teleost fish lineage.
To meet the constantly changing functional demands, the physiological properties of skeletal muscle are highly adjustable and are achieved through a process of switching muscle fiber-types, such as slow and fast muscle fibers, in response to internal and external stimuli, a process termed muscle fiber-type plasticity . Myosin heavy chains (MYHs) form a large gene family that includes sarcomeric MYHs, major contractile proteins of striated muscles that are expressed in a spatio-temporal manner defining the functional properties of different muscle fiber subtypes . In humans, sarcomeric MYHs form two clusters on the genome where skeletal and cardiac MYHs are arrayed in tandem on chromosome Chr17 and Chr14, respectively [2–5]. Upon completion of the human genome project, a novel MYH named MYH14 (MYH7b) was identified on Chr20 , recently, there has been increasing interest in its direct involvement in muscle fiber-type plasticity. Mammalian MYH14 has a microRNA, miR-499, in its 19th intron that suppresses the expression of genes involved in muscle fiber-type specification [7–11]; thus, miR-499 seemingly acts to support normal slow-muscle formation in mammals.
Our previous studies revealed that teleost fish also have MYH14 in their genomes [12, 13]. Expression analysis in torafugu Takifugu rubripes Abe 1949 and zebrafish Danio rerio Hamilton 1822 revealed that MYH14 is one of the major components of the MYH repertoire expressed in the slow and cardiac muscles of teleost fish [14, 15], suggesting its role in teleost muscle formation. Consistent with functional conservation with mammals, Wang et al.  showed that the transcriptional network of Sox6/MYH14/miR-499 plays an essential role in maintaining slow muscle lineage in larval zebrafish muscle. Our previous study also showed that teleost fish contain a higher number of MYHs in their genomes than do their mammalian counterparts [12, 13, 17, 18]. Two MYH14 paralogs, MYH M3383 and MYH M5 , were identified in the torafugu genome by phylogenetic and syntenic analyses . Moreover, we have also previously found that medaka Oryzias latipes lacks MYH14 in the syntenic region . These lines of evidence allowed us to speculate on the existence of a highly varied distribution and function of MYH14 and miR-499 in teleost fish.
The aim of this study was to elucidate the evolutionary history of MYH14/miR-499 in fish. MYH14 and miR-499 genes were screened from available vertebrate genome databases, and their evolutionary history was examined by synteny and phylogenetic analyses. In this study, we confirm the conversion of intronic into intergenic miRNA during fish evolution.
Distribution of MYH14 and miR-499 in teleost fish genomes
Gene IDs of MYH14 and miR-499 used in this study
Green spotted puffer
Green spotted puffer
Green spotted puffer
Phylogenetic analysis of MYH14 and miR-499
The miR-499s phylogenetic relationships (Figure 2B and Additional file 1: Figure S1B) were consistent with those of the MYH14s. Although the bootstrap value in each node was quite low, three zebrafish miR-499 paralogs, miR-499-1, -2, and −3, were divided into two clades. Zebrafish miR-499-1 formed a single cluster with other teleost fish miR-499s.
The combined phylogenetic and synteny analyses suggest that the MYH14/miR-499 locus was duplicated early in teleost evolution and one of the duplicated miR-499 genes was lost in the common ancestor to cod and the Acanthopterygii, after the split from the zebrafish lineage. Additionally, MYH14s have seemingly been lost at independent points of teleost evolution.
miR-499 expression in medaka
Sequence analysis of MYH14/miR-499 locus flanking regions
Secondary structure of the miR-499 stem-loop sequence
Intronic miRNA is transcribed as pre-mRNA from a part of an intron in the host gene . miRNA endowed by an intron folds to form a local double-stranded stem-loop structure called the primary miRNA (pri-miRNA). In animals, RNase III drosha crops pri-miRNA at the stem-loop during splicing and produces a precursor miRNA (pre-miRNA), which is then processed by dicer to form mature miRNA. From these canonical intronic miRNAs, a new type of intronic miRNA called mirtron has been discovered. Mirtrons are embedded in short introns, and their biogenesis does not require drosha cropping. The pre-miRNA of mirtron is produced directly by splicing [21–23]. Figure 4B shows miR-499 predicted stem-loop structures from medaka, torafugu, and the representative mirtron, miR-62, from Caenorhabditis elegans. miR-499s have longer stem-loop regions than those of mirtrons and are processed by drosha to produce pre-miRNAs. The torafugu MYH14 intron containing miR-499 is 247 bp in length (see Additional file 2: Figure S2), which is long enough to produce canonical miRNA hairpins to be cut by drosha. These results combined suggest that miR-499 is not a mirtron but a canonical intronic miRNA. However, experimental proof is required to confirm whether miR-499 requires drosha processing.
The existence of multiple MYH14 and miR-499 genes in various teleost fish suggests their expressional and functional versatilities. Torafugu MYH14-1 (MYH M5 ) expression was observed in both slow and cardiac muscles in the developmental and adult stages, whereas MYH14-2 (MYH M3383 ) expression was restricted to adult slow muscle [13, 14]. Zebrafish MYH14-1 was expressed in both slow and cardiac muscles in the early developmental stages and in slow and intermediate muscles in the adult stage . Furthermore, our present study demonstrates that medaka miR-499 expression differed from the above-mentioned MYH14expression patterns (see Figure 3). It would be interesting to determine whether such differences in MYH14 and miR-499 are related to physiological and ecological variations among teleost fish species. Fish are the most diverse vertebrate group consisting of over 22,000 species. In response to the wide range of environmental and physiological conditions they encounter, the characteristics of fish musculature, including muscle fiber-type composition, are also highly diverse. Medaka makes a particularly interesting subject because of the complete elimination of MYH14 from its genome. Although muscle fiber-type composition has not been well characterized in medaka, Ono et al.  reported an MYH gene specifically expressed in slow muscle fibers at the horizontal myoseptum. Such MYH expression has never been reported in other teleost fish species. In contrast, medaka fast muscle exhibits high plasticity to adapt to temperature fluctuations by changing MYH expression [18, 31]. Further comparative analyses of MYH14 and miR-499 may shed light on the mechanisms involved in the formation of species-specific musculature evolution.
The loss of the intronic miRNA in the ancestor of cod and the Acanthopterygii might be explained by functional redundancy. The loss of intronic miRNA from the host gene is possible if mutations are introduced into an intron without any effect on the function and expression of the host gene. Stickleback, medaka, and Atlantic cod display the opposite pattern with the intronic miRNA lacking its host gene. Intronic miRNAs are transcribed with their host genes, and thus, coordinated expression between an intronic miRNA and its host gene is frequently observed . In the present study, however, medaka miR-499 was actually expressed in various tissues despite the absence of MYH14 (see Figure 3). How does intronic miRNA remain after the loss of its host gene? We speculate that miR-499 is a canonical intronic miRNA produced by drosha cropping (see Figure 4B). Recent studies have revealed that splicing and pre-miRNA cropping by drosha are independent processes, indicating that splicing is not essential for intronic miRNA production . In other words, severe mutations of the host gene may not affect the production of intronic miRNAs in the presence of the host gene transcriptional system. Interestingly, sequence comparison analysis showed highly conserved 5′-flanking regions between torafugu MYH M5 and medaka miR-499 (see Figure 5A). The spatio-temporal expression of the major skeletal MYHs in teleost fish is regulated by small regions scattered throughout the 5′-flanking sequence [18, 30, 34, 35]. Recently, Yeung et al.  reported promoter activity in a 6.2-kb upstream sequence of mouse MYH14 that mimics endogenous MYH14 and miR-499 expression. Therefore, these conserved regions in the 5′-flanking sequence may act as a promoter for the spatio-temporal expression of MYH14, and the regulatory sequences are conserved in medaka miR-499 despite the loss of the MYH14 gene. We could also speculate that miR-499 has its own promoter as do some intronic miRNAs. In fact, Matthew et al.  reported uncoupled MYH14 and miRNA-499 expression in mice, suggesting the independent transcriptional regulation of miR-499 from MYH14. Isik et al.  found a conserved region immediately upstream of some intronic miRNAs in C. elegans and demonstrated in promoter activity the conserved region. An intronic sequence immediately downstream of miR-499 is conserved among zebrafish, torafugu, and medaka, as shown in Figure 4A, which could be the miR-499 promoter. These findings can potentially explain why miR-499 has remained despite the loss of MYH14 in some teleost fish genomes. To our knowledge, this is the first report that describes the conversion of intronic into non-intronic miRNA during evolution. Comparative analysis of transcriptional regulation between intronic and intergenic miR-499s will provide new insights into miRNA evolution.
All procedures in this study were performed according to the Animal Experimental Guidelines for The University of Tokyo. Live adult medaka specimens (average body weight of 0.78 g) were reared in local tap water with a circulating system at 28.5°C under a 14:10-h light–dark photoperiod, at a fish rearing facility in the Department of Aquatic Bioscience, The University of Tokyo. Tissue for RNA extraction was dissected after instant euthanasia by decapitation and stored in RNAlater (Invitrogen, San Diego, CA, USA). Embryos were obtained by natural spawning and raised at 28.5°C. The developmental stage was determined by the number of days post fertilization.
Construction of a physical map around MYH14 and miR-499
The Ensembl genome browser (http://www.ensembl.org/index.html) was used to determine the syntenic organization in the region surrounding MYH14 and/or miR-499 in vertebrates. The database versions used were as follows: human (GRCh37), chicken (Galgal4), coelacanth L. chalumnae (LatCha1), zebrafish D. rerio (Zv9), torafugu T. rubripes (FUGU4), green spotted puffer T. nigroviridis (TETRAODON8), tilapia O. niloticus (Orenil1.0), Atlantic cod G. morhua (gadMor1), stickleback G. aculeatus (BROADS1), platyfish X. maculatus (Xipmac4.4.2), and medaka O. latipes (MEDAKA1). The pre Ensembl browser (http://pre.ensembl.org/index.html) was used for analysis of spotted gar L. oculatus (LepOcu1).
The MYH14 and miR-499 sequence data were retrieved from the available genome databases mentioned above (Table 1). NJ and ML trees were constructed on the basis of the MYH14 coding and miR-499 stem-loop sequences using MEGA5  with 1000 bootstrap replications. The Nei and Gojyobori method  (Jukes-Cantor) was employed to consider synonymous and non-synonymous substitutions for the MYH14 NJ tree. The Tajima-Nei model  was employed for the miR-499 NJ tree, whereas the Tamura-Nei model  was used for the MYH14 and miR-499 ML trees. The torafugu MYH14-1 (MYH M5 ), zebrafish MYH14-1 5′- and 3′-flanking sequences, and the medaka miR-499 stem-loop sequences, which contain Snai1 and TRPC4AP genes, were retrieved from the Ensembl genome browser. The homology search on the flanking sequences was carried out using the mVISTA alignment program through the vista server (http://genome.lbl.gov/vista/index.shtml). Putative secondary structures of the miR-499 from medaka and torafugu stem-loop sequences and that of the C. elegans mirtron miR-62 (miRBase accession number: MI0000033) were predicted using the RNA fold program CentroidFold (http://www.ncrna.org/centroidfold).
Small RNA library construction and sequencing
Total RNA was extracted from the muscle, intestine, eye, brain, heart, ovary, and testis of adult medaka using a mirVana™ miRNA Isolation Kit (Applied Biosystems, Foster City, CA, USA). Small RNAs (less than 40 nucleotides in size) were purified from total RNA using a flashPAGE™ Fractionator (Applied Biosystems), and the small RNA libraries were constructed according to the manufacturer’s instructions. Library sequencing was performed with SOLiD™ next-generation sequencer (Applied Biosystems). After elimination of low-quality reads using perl scripts of our own design, 102, 602, 452 reads of 35 nucleotides were obtained. The 18–25 nucleotide reads were subjected to a Blast search against known mature miRNA sequences deposited in miRBase 18.0 (http://www.mirbase.org/). The sequences with their seed regions (2–8 nucleotides from the 5′-end) showing 100% identity to those of known mature miR-499 sequences were annotated as medaka miR-499. Gene expression was represented as reads per million (RPM), which corresponds to (total reads of a given gene/total reads in the tissue) × 106. Sequence data sets used in this study were deposited at the DDBJ Sequence Read Archive under the accession number DRA001039 and DRA001040.
In situ hybridization
We used a digoxigenin (DIG)-labeled MiRCURY detection probe (Exiqon, Copenhagen, Denmark), an LNA-modified oligo DNA probe containing the miR-499 mature sequence (5′-AAACATCACTGCAAGTCTTAA-3′), to detect miR-499 transcripts. In situ hybridizations were performed according to Kloosterman et al. . The adult, embryo, and larval medaka trunk skeletal and cardiac muscles were fixed in 4% PFA at 4°C overnight. Transverse sections of the tissues were cut at 16-μm thickness. All hybridizations were performed at 66°C, which was 20°C below the predicted melting temperature (Tm) of the LNA probe. Alkaline phosphatase-conjugated anti-DIG antibody (Roche Diagnostics, Penzberg, Germany) and nitroblue tetrazolium chloride/5-bromo-4-chloro-3-indolyl phosphate were used for signal detection with an MVX10 stereomicroscope (Olympus, Tokyo, Japan).
This study was partly supported by a Grant-in Aid for Scientific research from the Japan Society for the Promotion of Science.
- Schiaffino S, Reggiani C: Fiber types in mammalian skeletal muscles. Physiol Rev. 2011, 91: 1447-1531. 10.1152/physrev.00031.2010.PubMedView ArticleGoogle Scholar
- Mahdavi V, Chambers AP, Nadal-Ginard B: Cardiac alpha- and beta-myosin heavy chain genes are organized in tandem. Proc Natl Acad Sci USA. 1984, 81: 2626-2630. 10.1073/pnas.81.9.2626.PubMed CentralPubMedView ArticleGoogle Scholar
- Saez LJ, Gianola KM, McNally EM, Feghali R, Eddy R, Shows TB, Leinwand LA: Human cardiac myosin heavy chain genes and their linkage in the genome. Nucleic Acids Res. 1987, 15: 5443-5459. 10.1093/nar/15.13.5443.PubMed CentralPubMedView ArticleGoogle Scholar
- Weiss A, McDonough D, Wertman B, Acakpo-Satchivi L, Montgomery K, Kucherlapati R, Leinwand L, Krauter K: Organization of human and mouse skeletal myosin heavy chain gene clusters is highly conserved. Proc Natl Acad Sci USA. 1999, 96: 2958-2963. 10.1073/pnas.96.6.2958.PubMed CentralPubMedView ArticleGoogle Scholar
- Shrager JB, Desjardins PR, Burkman JM, Konig SK, Stewart SK, Su L, Shah MC, Bricklin E, Tewari M, Hoffman R, Rickels MR, Jullian EH, Rubinstein NA, Stedman HH: Human skeletal myosin heavy chain genes are tightly linked in the order embryonic-IIa-IId/x-ILb-perinatal-extraocular. J Muscle Res Cell Motil. 2000, 21: 345-355. 10.1023/A:1005635030494.PubMedView ArticleGoogle Scholar
- Desjardins PR, Burkman JM, Shrager JB, Allmond LA, Stedman HH: Evolutionary implications of three novel members of the human sarcomeric myosin heavy chain gene family. Mol Biol Evol. 2002, 19: 375-393. 10.1093/oxfordjournals.molbev.a004093.PubMedView ArticleGoogle Scholar
- van Rooij E, Quiat D, Johnson BA, Sutherland LB, Qi X, Richardson JA, Kelm RJ, Olson EN: A family of microRNAs encoded by myosin genes governs myosin expression and muscle performance. Dev Cell. 2009, 17: 662-673. 10.1016/j.devcel.2009.10.013.PubMed CentralPubMedView ArticleGoogle Scholar
- Bartel DP: MicroRNAs: genomics, biogenesis, mechanism, and function. Cell. 2004, 116: 281-297. 10.1016/S0092-8674(04)00045-5.PubMedView ArticleGoogle Scholar
- McCarthy JJ, Esser AK, Peterson AC, Dupont-Versteegden EE: Evidence of MyomiR network regulation of β-myosin heavy chain gene expression during skeletal muscle atrophy. Physiol Genomics. 2009, 39: 219-226. 10.1152/physiolgenomics.00042.2009.PubMed CentralPubMedView ArticleGoogle Scholar
- Hagiwara N, Yeh M, Liu A: Sox6 is required for normal fiber type differentiation of fetal skeletal muscle in mice. Dev Dyn. 2007, 236: 2062-2076. 10.1002/dvdy.21223.PubMedView ArticleGoogle Scholar
- von Hofsten J, Elworthy S, Gilchrist MJ, Smith JC, Wardle FC, Ingham PW: Prdm1- and Sox6-mediated transcriptional repression specifies muscle fiber type in the zebrafish embryo. EMBO Rep. 2008, 9: 683-689. 10.1038/embor.2008.73.PubMed CentralPubMedView ArticleGoogle Scholar
- Watabe S, Ikeda D: Diversity of the pufferfish Takifugu rubripes fast skeletal myosin heavy chain genes. Comp Biochem Physiol. 2006, 1: 28-34.Google Scholar
- Ikeda D, Ono Y, Snell P, Edwards YJ, Elgar G, Watabe S: Divergent evolution of the myosin heavy chain gene family in fish and tetrapods: evidence from comparative genomic analysis. Physiol Genomics. 2007, 32: 1-15. 10.1152/physiolgenomics.00278.2006.PubMedView ArticleGoogle Scholar
- Akolkar DB, Kinoshita S, Yasmin L, Ono Y, Ikeda D, Yamaguchi H, Nakaya M, Erdogan O, Watabe S: Fibre type-specific expression patterns of myosin heavy chain genes in adult torafugu Takifugu rubripes muscles. J Exp Biol. 2010, 213: 137-145. 10.1242/jeb.030759.PubMedView ArticleGoogle Scholar
- Kinoshita S, Bhuiyan SS, Ceyhun SB, Asaduzzaman M, Asakawa S, Watabe S: Species-specific expression variation of fish MYH14, an ancient vertebrate myosin heavy chain gene orthologue. Fish Sci. 2011, 77: 847-853. 10.1007/s12562-011-0375-2.View ArticleGoogle Scholar
- Wang X, Ono Y, Tan CS, Chai RJ, Philip C, Ingham PW: Prdm1a and miR-499 act sequentially to restrict Sox6 activity to the fast-twitch muscle lineage in the zebrafish embryo. Development. 2011, 138: 4399-4404. 10.1242/dev.070516.PubMedView ArticleGoogle Scholar
- Ikeda D, Clark MS, Liang CS, Snell P, Edwards YJK, Elgar G, Watabe S: Genomic structural analysis of the pufferfish (Takifugu rubripes) skeletal muscle myosin heavy chain genes. Mar Biotechnol. 2004, 6: S462-S467.Google Scholar
- Liang CS, Kobiyama A, Shimizu A, Sasaki T, Asakawa S, Shimizu N, Watabe S: Fast skeletal muscle myosin heavy chain gene cluster of medaka Oryzias latipes enrolled in temperature adaptation. Physiol Genomics. 2007, 29: 201-214.PubMedView ArticleGoogle Scholar
- Monteys AM, Spengler RM, Wan J, Tecedor L, Lennox KA, Xing Y, Davidson BL: Structure and activity of putative intronic miRNA promoters. RNA. 2010, 16: 495-505. 10.1261/rna.1731910.PubMed CentralPubMedView ArticleGoogle Scholar
- Kim VN, Han J, Siomi MC: Biogenesis of small RNAs in animals. Nat Rev Mol Cell Biol. 2009, 10: 126-139. 10.1038/nrm2632.PubMedView ArticleGoogle Scholar
- Berezikov E, Chung WJ, Willis J, Cuppen E, Lai EC: Mammalian mirtron genes. Mol Cell. 2007, 28: 328-336. 10.1016/j.molcel.2007.09.028.PubMed CentralPubMedView ArticleGoogle Scholar
- Okamura K, Hagen JW, Duan H, Tyler DM, Lai EC: The mirtron pathway generates microRNA-class regulatory RNAs in drosophila. Cell. 2007, 130: 89-100. 10.1016/j.cell.2007.06.028.PubMed CentralPubMedView ArticleGoogle Scholar
- Ruby JG, Jan CH, Bartel DP: Intronic microRNA precursors that bypass drosha processing. Nature. 2007, 448: 83-86. 10.1038/nature05983.PubMed CentralPubMedView ArticleGoogle Scholar
- Amores A, Force A, Yan YL, Joly L, Amemiya C, Fritz A, Ho RK, Langeland J, Prince V, Wang YL, Westerfield M, Ekker M, Postlethwait JH: Zebrafish hox clusters and vertebrate genome evolution. Science. 1998, 282: 1711-1714.PubMedView ArticleGoogle Scholar
- Elgar G, Clark MS, Meek S, Smith S, Warner S, Edwards YJ, Bouchireb N, Cottage A, Yeo GS, Umrania Y, Williams G, Brenner S: Generation and analysis of 25 Mb of genomic DNA from the pufferfish Fugu rubripes by sequence scanning. Genome Res. 1999, 9: 960-971. 10.1101/gr.9.10.960.PubMed CentralPubMedView ArticleGoogle Scholar
- Postlethwait JH, Woods IG, Ngo-Hazelett P, Yan YL, Kelly PD, Chu F, Huang H, Hill-Force A, Talbot WS: Zebrafish comparative genomics and the origins of vertebrate chromosomes. Genome Res. 2000, 10: 1890-1902. 10.1101/gr.164800.PubMedView ArticleGoogle Scholar
- Woods IG, Kelly PD, Chu F, Ngo-Hazelett P, Yan YL, Huang H, Postlethwait JH, Talbot WS: A comparative map of the zebrafish genome. Genome Res. 2000, 10: 1903-1914. 10.1101/gr.10.12.1903.PubMed CentralPubMedView ArticleGoogle Scholar
- Smith SF, Snell P, Gruetzner F, Bench AJ, Haaf T, Metcalfe JA, Green AR, Elgar G: Analyses of the extent of shared synteny and conserved gene orders between the genome of Fugu rubripes and human 20q. Genome Res. 2002, 12: 776-784.PubMed CentralPubMedView ArticleGoogle Scholar
- Hoegg S, Brinkmann H, Taylor JS, Meyer A: Phylogenetic timing of the fish-specific genome duplication correlates with the diversification of the teleost fish. J Mol Evol. 2004, 59: 190-203. 10.1007/s00239-004-2613-z.PubMedView ArticleGoogle Scholar
- Ono Y, Kinoshita S, Ikeda D, Watabe S: Early development of medaka Oryzias latipes muscles as revealed by transgenic approaches using embryonic and larval types of myosin heavy chain genes. Dev Dyn. 2010, 239: 1807-1817. 10.1002/dvdy.22298.PubMedView ArticleGoogle Scholar
- Liang CS, Ikeda D, Kinoshita S, Shimizu A, Sasaki T, Asakawa S, Shimizu N, Watabe S: Myocyte enhancer factor 2 regulates expression of medaka Oryzias latipes fast skeletal myosin heavy chain genes in a temperature-dependent manner. Gene. 2008, 407: 42-53. 10.1016/j.gene.2007.09.016.PubMedView ArticleGoogle Scholar
- Baskerville S, Bartel DP: Microarray profiling of microRNAs reveals frequent coexpression with neighboring miRNAs and host genes. RNA. 2005, 11: 241-247. 10.1261/rna.7240905.PubMed CentralPubMedView ArticleGoogle Scholar
- Kim YK, Kim VN: Processing of intronic microRNAs. EMBO J. 2007, 26: 775-783. 10.1038/sj.emboj.7601512.PubMed CentralPubMedView ArticleGoogle Scholar
- Yasmin L, Kinoshita S, Akolkar DB, Asaduzzaman M, Ikeda D, Ono Y, Watabe S: A 5′-flanking region of embryonic-type myosin heavy chain gene, MYH M743-2 , from torafugu (Takifugu rubripes) regulates developmental muscle-specific expression. Comp Biochem Physiol. 2010, 6: 76-81.Google Scholar
- Asaduzzaman M, Kinoshita S, Bhuiyan SS, Asakawa S, Watabe S: Multiple cis-elements in the 5′-flanking region of embryonic/larval fast-type of the myosin heavy chain gene of torafugu, MYH M743-2 , function in the transcriptional regulation of its expression. Gene. 2011, 489: 41-54. 10.1016/j.gene.2011.08.005.PubMedView ArticleGoogle Scholar
- Yeung F, Chung E, Guess MG, Bell ML, Leinwand LA: Myh7b/miR-499 gene expression is transcriptionally regulated by MRFs and EOS. Nucleic Acids Res. 2012, 40: 7303-7318. 10.1093/nar/gks466.PubMed CentralPubMedView ArticleGoogle Scholar
- Matthew LB, Massimo B, Leslie AL: Uncoupling of expression of an intronic microRNA and its myosin host gene by exon skipping. Mol Cell Biol. 2010, 30: 1937-1945. 10.1128/MCB.01370-09.View ArticleGoogle Scholar
- Isik M, Hendrik CK, Berezikov E: Expression patterns of intronic microRNAs inCaenorhabditis elegans. Silence. 2010, 1: 1-5. 10.1186/1758-907X-1-1.View ArticleGoogle Scholar
- Tamura K, Peterson D, Peterson N, Stecher G, Nei M, Kumar S: MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol. 2011, 28: 2731-2739. 10.1093/molbev/msr121.PubMed CentralPubMedView ArticleGoogle Scholar
- Nei M, Gojobori T: Simple methods for estimating the numbers of synonymous and nonsynonymous nucleotide substitutions. Mol Biol Evol. 1986, 3: 418-426.PubMedGoogle Scholar
- Tajima F, Nei M: Estimation of evolutionary distance between nucleotide sequences. Mol Biol Evol. 1984, 1: 269-285.PubMedGoogle Scholar
- Tamura K, Nei M: Estimation of the number of nucleotide substitutions in the control region of mitochondrial DNA in humans and chimpanzees. Mol Biol Evol. 1993, 10: 512-526.PubMedGoogle Scholar
- Kloosterman WP, Wienholds E, de Bruijn E, Kauppinen S, Plasterk RH: In situ detection of miRNAs in animal embryos using LNA-modified oligonucleotide probes. Nat Methods. 2006, 3: 27-29. 10.1038/nmeth843.PubMedView ArticleGoogle Scholar
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