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目的:研究表明β-珠蛋白基因在发育过程中呈现选择表达的转换机制,其上游的基因座位点控制区(LCR)调控了β-珠蛋白基因家族的表达模式。为了深入探究β-珠蛋白基因表达调控的分子网络,本文对其他可能参与调控β-珠蛋白基因表达的远程调控元件进行筛选,对β-珠蛋白基因动态调控转换机制进行深入研究。方法:早幼粒细胞经全反式维甲酸诱导分化,以β-珠蛋白基因启动子区及LCR作为环形染色体构象捕获(4C)技术分析的靶位点,通过测序技术与调控元件分析结合,在全基因组筛选与β-珠蛋白家族基因座位发生相互作用关系的位点。结果:根据4C测序结果,筛选出与HBD启动子区及LCR存在相互作用关系的位点。通过染色体构象捕获(3C)验证,结果与测序结果一致。通过甲醛辅助分离调控元件技术及Epiregio在线网站对调控元件功能性分析,结果表明筛选位点AC105129.4、AL354707.17、AC078785.22及AC021646.35均为潜在的参与β-珠蛋白基因调控元件。结论:4C筛选位点与锚定位点相互作用表明了β-珠蛋白家族基因座位在细胞核内复杂的空间组织形式。
Abstract:Objective:Studies have shown that β-globin gene presents a selective expression transformation mechanism during development,and its upstream locus control region(LCR)regulates the expression pattern of β-globin gene family. To further explore the molecular network of β-globin gene expression regulation,other long-range regulatory elements that may be involved in the regulation of β-globin gene expression were screened and the dynamic regulation and transformation mechanism of β-globin gene was deeply studied. Methods:Promyelocytic cells were induced to differentiate by all-trans retinoic acid. β-globin gene promoter region and LCR were used as the target sites for circular chromosome conformational capture(4C) analysis.Through sequencing and regulatory element analysis,the sites interacting with β-globin family loci were screened in the whole genome. Results:According to the results of 4C sequencing,the sites that interact with HBD promoter region and LCR were screened. Verified by chromosome conformational capture(3C),the results were consistent with those of sequencing. The functional analysis of regulatory elements by formaldehyde-assisted separation regulatory elements and Epiregio online website showed that the screening sites AC105129.4,AL354707.17,AC078785.22 and AC021646.35 were all potential regulatory elements involved in β-globin gene. Conclusion:The interaction between 4C screening site and anchor site showed the complex spatial organization of β-globin family loci in the nucleus.
1 Kong N,Jung I. Long-range chromatin interactions in pathogenic gene expression control[J]. Transcription,2020,11(5):211-216.
2 Iarovaia OV,Kovina AP,Petrova NV,et al. Genetic and epigenetic mechanisms of β-globin gene switching[J]. Biochemistry(Mosc),2018,83(4):381-392.
3 Kong S,Zhang Y. Deciphering Hi-C:from 3D genome to function[J]. Cell Biol Toxicol,2019,35(1):15-32.
4 Zhao Z,Tavoosidana G,Sjolinder M,et al. Circular chromosome conformation capture(4C)uncovers extensive networks of epigenetically regulated intra-and interchromosomal interactions[J]. Nat Genet, 2006, 38(11):1341-1347.
5 Grob S,Cavalli G. Technical review:A Hitchhiker's guide to chromosome conformation capture[J]. Methods Mol Biol,2018,1675:233-246.
6 McCord RP,Kaplan N,Giorgett L. Chromosome conformation capture and beyond:Toward an integrative view of chromosome structure and function[J]. Mol Cell,2020,77(4):688-708.
7 Ju JY,Zhao Q. Regulation of gamma-globin gene expression and its clinical applications[J]. Yi Chuan,2018,40(6):429-444.
8 Thein SL. Molecular basis of beta thalassemia and potential therapeutic targets[J]. Blood Cells Mol Dis,2018,70:54-65.
9 Li Q,Peterson KR,Fang X,et al. Locus control regions[J]. Blood,2002,100(9):3077-3086.
10 Brand?o HB,Gabriele M,Hansen AS. Tracking and interpreting long-range chromatin interactions with superresolution live-cell imaging[J]. Curr Opin Cell Biol,2021,70:18-26.
11 Dekker J. A closer look at long-range chromosomal interactions[J]. Trends Biochem Sci,2003,28(6):277-280.
12 Ethier SD,Miura H,Dostie J. Discovering genome regulation with 3C and 3C-related technologies[J]. Biochim Biophys Acta,2012,1819(5):401-410.
13 Tian H,Yang Z,Xu X,et al. Three-dimensional chromosome conformation capture and its derived technologies[J]. Sheng Wu Gong Cheng Xue Bao,2020,36(10):2040-2050.
14 任立成,李美英,孙元田,等.利用环形染色体构象捕获技术对Bcl11b基因座位在细胞核内空间组织的研究[J].中国细胞生物学学报,2013,35(11):1584-1591.
15 Alfonso R,Tabea R,Olesja R,et al. Formaldehyde-assisted isolation of regulatory elements to measure chromatin accessibility in mammalian cells[J]. J Vis Exp,2018,134:1-8.
16 Baumgarten N,Hecker D,Karunanithi S,et al. EpiRegio:Analysis and retrieval of regulatory elements linked to genes[J]. Nucleic Acids Res,2020,48(1):193-199.
17 Dekker J,Rippe K,Dekker M,et al. Capturing chromosome conformation[J]. Science,2002,295(5558):1306-1311.
18 Ren L,Shi M,Wang Y,et al. CTCF and cohesin cooperatively mediate the cell-type specific interchromatin interaction between Bcl11b and Arhgap6 loci[J]. Mol Cell Biochem,2012,360(1/2):243-251.
19 Ren L,Wang Y,Shi M,et al. CTCF mediates the celltype specific spatial organization of the Kcnq5 locus and the local gene regulation[J]. PLoS One,2012,7(2):314-316.
20 Xi H,Shulha HP,Lin JM,et al. Identification and characterization of cell type-specific and ubiquitous chromatin regulatory structures in the human genome[J]. PLoS Genet,2007,3(8):e136.
21 McKay DJ. Using Formaldehyde-Assisted Isolation of Regulatory Elements(FAIRE)to Identify Functional Regulatory DNA in Insect Genomes[J]. Methods Mol Biol,2019,1858:89-97.
22 Kang J,Kim YW,Park S,et al. Multiple CTCF sites cooperate with each other to maintain a TAD for enhancer-promoter interaction in the β-globin locus[J]. FASEB J,2021,35(8):e21768.
23 Oomen ME,Hansen AS,Liu Y,et al. CTCF sites display cell cycle-dependent dynamics in factor binding and nucleosome positioning[J]. Genome Res,2019,29(2):236-249.
24 Chowdhary S,Kainth AS,Gross DS. Chromosome conformation capture that detects novel cis-and trans-interactions in budding yeast[J]. Methods,2020,170:4-16.
25 Oudelaar AM,Beagrie RA,Gosden M,et al. Dynamics of the 4D genome during in vivo lineage specification and differentiation[J]. Nat Commun,2020,11(1):2722.
26 Azagra A,Marina-Zárate E,Ramiro AR,et al. From loops to looks:Transcription factors and chromatin organization shaping terminal B cell differentiation[J].Trends Immunol,2020,41(1):46-60.
27 Gurumurthy A,Yu DT,Stees JR,et al. Super-enhancer mediated regulation of adult β-globin gene expression:The role of eRNA and Integrator[J]. Nucleic Acids Res,2021,49(3):1383-1396.
28 Van de Werken HJ,De Vree PJ,Splinter E,et al. 4C technology:Protocols and data analysis[J]. Methods Enzymol,2012,513:89-112.
29 Walter C,Schuetzmann D,Rosenbauer F,et al. Benchmarking of 4C-seq pipelines based on real and simulated data[J]. Bioinformatics,2019,35(23):4938-4945.
30 Krijger PHL,Geeven G,Bianchi V,et al. 4C-seq from beginning to end:A detailed protocol for sample preparation and data analysis[J]. Methods,2020,170:17-32.
基本信息:
DOI:10.13210/j.cnki.jhmu.20220906.002
中图分类号:R346
引用信息:
[1]肖亦舒,许兰,刘春亚,等.β-珠蛋白基因远程相互作用元件的筛选与功能性分析[J].海南医学院学报,2022,28(24):1841-1847.DOI:10.13210/j.cnki.jhmu.20220906.002.
基金信息:
国家自然科学基金项目(31660318); 海南省自然科学基金高层次人才项目(820RC638); 海南省研究生创新课题(Hys2020-377)~~
2022-09-06
2022-09-06
2022-09-06