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Cloning and Bioinformatics Analysis of Alternatively Spliced Variants of HSF1 Gene in Dairy Cattle (Bos taurus) |
QI Ying1, ZHANG Yi-Ming1, ZHAO Meng-Yun1, HUANG Mei-Qi1, GUO Yue-Mei1, CHU Ming-Xing2, LI Qiu-Ling1,* |
1 Hebei Key Laboratory of Animal Diversity/College of Life Sciences, Langfang Normal University, Langfang 065000, China; 2 Key Laboratory of Animal (Poultry) Genetics Breeding and Reproduction, Ministry of Agriculture and Rural Affairs/Institute of Animal Science, Chinese Academy of Agricultural Sciences, Beijing 100193, China |
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Abstract Heat shock transcription factor 1 (HSF1) is an important transcription factor that initiates heat shock protein gene expression. Further study on HSF1 will help to clarify the regulatory mechanism of HSF1 on heat stress response. In this study, reverse transcription-PCR (RT-PCR) was used to clone the full-length CDS of HSF1 from Chinese Holstein cow (Bos taurus), and bioinformatics was used to analyze the biological characteristics of the protein. The results showed that 3 splice variants were successfully cloned, named HSF1-AS1 (GenBank No. MW401766), HSF1-AS2 (GenBank No. XM_005215151.4), and HSF1-AS3 (GenBank No. MW401767). The splicing patterns of the 3 variants were exon skipping, intron retaining, and alternative 3' splice sites. The ORF analysis showed that the 3 splice variants of HSF1 encoded 311, 553 and 517 aa, respectively. The RNA-seq data of breast tissue in previous study was analyzed, and the results showed that the expression of HSF1-AS2 was the highest (P<0.01), and the expression of HSF1-AS1 was the lowest (P<0.01). The results of qRT-PCR showed that the expression levels of HSF1-AS1 and HSF1-AS2 were both up-regulated in heat stressed mammary epithelial cells. The binding site analysis of splicing factors showed that the SNP (18948 C>T) of exon 11 of HSF1 gene was just in the potential region of exonic splicing enhancer (ESE), which might be associated with the formation of HSF1-AS3. The phylogenetic analysis showed that bovine HSF1 amino acid sequence had high homology and close genetic distance with that of goats (Capra hircus). The present study provides a reference for further elucidating the regulation mechanism of HSF1 gene expression.
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Received: 16 December 2020
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Corresponding Authors:
* liqiuling@lfnu.edu.cn
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[1] 耿红红, 张敬旸, 李莲, 等. 2016. RNA-seq转录组测序分析不同季节对槟榔江水牛精液品质的影响[J]. 畜牧兽医学报, 47(7): 1373-1380. (Geng H H, Zhang J Y, Li L, et al.2016. Semen quality analysis of Betelnut-jiang buffalo in different seasons by RNA-seq[J]. Acta Veterinaria et Zootechnica Sinica, 47(7): 1373-1380.) [2] Baralle F E, Giudice J.2017. Alternative splicing as a regulator of development and tissue identity[J]. Nature Reviews Molecular Cell Biology, 18(7): 437-451. [3] Bush S J, Chen L, Tovar-Corona J M, et al.2017. Alternative splicing and the evolution of phenotypic novelty[J]. Philosophical Transactions of the Royal Society B, 372(1713): 20150474. [4] Cartegni L, Wang J, Zhu Z, et al.2003. ESE finder: A web resource to identify exonic splicing enhancers[J]. Nucleic Acid Research, 31(13): 3568-3571. [5] Crick F.1979. Split genes and RNA splicing[J]. Science, 204(4390): 264-271. [6] Drögemüller C, Reichart U, Seuberlich T, et al.2011. An unusual splice defect in the mitofusin 2 gene (MFN2) is associated with degenerative axonopathy in Tyrolean Grey cattle[J]. PLOS ONE, 6(4): e18931. [7] Feng H, Qin Z, Zhang X.2013. Opportunities and methods for studying alternative splicing in cancer with RNA-Seq[J]. Cancer Letters, 340(2): 179-191. [8] Gabut M, Mine M, Marsac C, et al.2005. The SR protein SC35 is responsible for aberrant splicing of the E1α pyruvate dehydrogenase mRNA in a case of mental retardation with lactic acidosis[J]. Molecular & Cellular Biology, 25(8): 3286-3294. [9] Grau-Bove X, Ruiz-Trillo I, Irimia M.2018. Origin of exon skipping-rich transcriptomes in animals driven by evolution of gene architecture[J]. Genome Biology, 19(1): 135. [10] Hahn M A, Mcdonnell J, Marsh D J.2009. The effect of disease associated HRPT2 mutations on splicing[J]. Journal of Endocrinology, 201(3): 387-96. [11] Haltenhof T, Kotte A, De Bortoli F, et al.2020. A conserved kinase-based body temperature sensor globally controls alternative splicing and gene expression[J]. Molecular Cell, 78(1): 57-69. [12] Horton P, Park K J, Obaysshi T, et al.2007. WoLF PSORT: Protein localization predictor[J]. Nucleic Acids Research, 35(Web Server issue): W585-W587. [13] Lee Y, Rio D C.2015. Mechanisms and regulation of alternative pre-mRNA splicing[J]. Annual Review of Biochemistry, 84(1): 291-323. [14] Li Q L, Qiao J, Zhang Z F, et al.2020. Identification and analysis of differentially expressed long non-coding RNAs of Chinese Holstein cattle responses to heat stress[J]. Animal Biotechnology, 31(1): 9-16. [15] Merkin J,Russell C,Chen P,et al.2012. Evolutionary dynamics of gene and isoform regulation in mammalian tissues[J]. Science, 338(6114): 1593-1599 [16] Mcvety S, Li L, Gordon P H, et al.2006. Disruption of an exon splicing enhancer in exon 3 of MLH1 is the cause of HNPCC in a Quebec family[J]. Journal of Medical Genetics, 43(2): 153-156. [17] Nilsen T W, Graveley B R.2010. Expansion?of the?eukaryotic?proteome?by alternative splicing[J]. Nature, 463(7280): 457-463. [18] Patro R, Duggal G, Love M I, et al.2017. Salmon provides fast and bias-aware quantification of transcript expression[J]. Nature Methods, 14(4): 417-419. [19] Quesnel-Vallieres M, Irimia M, Cordes S P, et al.2015. Essential roles for the splicing regulator nSR100/SRRM4 during nervous system development[J]. Genes Development, 29(7): 746-759. [20] Rong Y, Zeng M, Guan X, et al.2019. Association of HSF1 genetic variation with heat tolerance in Chinese cattle[J]. Animals, 9(12): 1027-1033. [21] Strandness E, Bernstein D.1997. Developmental and afterload stress regulation of heat shock proteins in the ovine myocardium[J]. Pediatric Research, 41(1): 51-56. [22] Vania G, Peter J.2015. Posttranscriptional regulation of splicing factor SRSF1 and its role in cancer cell biology[J]. BioMed Research International, 2015: 287048. [23] Wang X, Zhong J, Gao Y, et al.2014. A SNP in intron 8 of CD46 causes a novel transcript associated with mastitis in Holsteins[J]. BMC Genomics, 15(1): 1-11. |
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