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转录因子PU.1和KLF7在脂肪形成、造血分化、肿瘤发生和机体免疫等方面发挥重要作用,但是两者在功能上是否具有相关性尚不清楚。本研究旨在研究PU.1和KLF7在小鼠不同组织中的表达模式及相关性。利用RT-qPCR检测PU.1和KLF7在小鼠胃、肝脏、空肠、肺、腿肌、心脏、脂肪、胸肌、脾脏、肾脏和脑组织中的表达情况,并分析表达相关性。结果显示,KLF7在肺、胃和脂肪中的表达量较高,PU.1在肺、肝脏和脾脏中的表达量较高;两个基因的表达呈极显著正相关(r=0.857, P=0.001)。生物信息学预测显示,在KLF7的5'侧翼区共存在5个PU.1的结合位点,PU.1可能正调控KLF7基因的表达。本研究为深入研究PU.1和KLF7的功能及相互作用机制提供重要的基础数据。
Abstract:Transcription factors PU.1 and KLF7 play important roles in adipogenesis, hematopoiesis, tumorigenesis, and body immune, but whether they are functionally related is unclear. The purpose of this study was to investigate the expression pattern and correlation of PU.1 and KLF7 in different tissue of mices. The expressions of PU.1 and KLF7 in the stomach, liver, jejunum, lung, leg muscle, heart, fat, chest muscle, spleen, kidney and brain tissues of mice were detected by RT-qPCR, and the correlation was analyzed. The results showed that KLF7 was highly expressed in lung, stomach and fat, and PU.1 was highly expressed in lung, liver and spleen. The expression of the two genes was significantly positively correlated(r=0.857, P=0.001). Bioinformatics prediction showed that there were 5 binding sites of PU.1 located in the 5'-flanking region of KLF7, which may regulate the expression of KLF7 gene. This study provided important basic data for in-depth study of the function and interaction mechanism of PU.1 and KLF7.
Bhat tarai S.,Socha cka-Marlowe A.,Crutchfield G.,Khan R.,Londraville R.,and Liu Q.,2016,Krüppel-like factors 7 and6a m RNA expression in adult zebrafish central nervous system,Gene Expr.Patterns,21(1):41-53.
Blackmore M.G.,Wang Z.,Lerch J.K.,Motti D.,Zhang Y.P.,Shields C.B.,Lee J.K.,Goldberg J.L.,Lemmon V.P.,and Bixby J.L.,2012,Krüppel-like factor 7 engineered for transcriptional activation promotes axon regeneration in the adult corticospinal tract,Proc.Natl.Acad.Sci.USA,109(19):7517-7522.
Carey H.A.,Hildreth B.E.,Samuvel D.J.,Thies K.A.,Rosol T.J.,Toribio R.E.,Charles J.F.,Ostrowski M.C.,and Sharma S.M.,2019,Eomes partners with PU.1 and MITF to regulate transcription factors critical for osteoclast differentiation,Iscience.,11:238-245.
Etzrodt M.,Ahmed N.,Hoppe P.S.,Loeffler D.,Skylaki S.,Hilsenbeck O.,Kokkaliaris K.D.,Kaltenbach H.M.,Stelling J.,Nerlov C.,and Schroeder T.,2019,Inflammatory signals directly instruct PU.1 in HSCs via TNF,Blood,133 (8):816-819.
Fischer J.,Walter C.,Tonges A.,Aleth H.,Jordao M.J.C.,Leddin M.,Groning V.,Erdmann T.,Lenz G.,Roth J.,Vogl T.,Prinz M.,Dugas M.,Jacobsen I.D.,and Rosenbauer F.,2019,Safeguard function of PU.1 shapes the inflammatory epigenome of neutrophils,Nat.Immunol.,20(5):546-558.
Flotho C.,Coustan-Smith E.,Pei D.Q.,Cheng C.,Song G.C.,Pui C.H.,Downing J.R.,and Campana D.,2007,A set of genes that regulate cell proliferation predicts treatment outcome in childhood acute lymphoblastic leukemia,Blood,110 (4):1271-1277.
Gupta P.,Gurudutta G.U.,Saluja D.,and Tripathi R.P.,2009,PU.1 and partners:regulation of haematopoietic stem cell fate in normal and malignant haematopoiesis,J.Cell.Mol.Med.,13(11-12):4349-4363.
Izawa N.,Kurotaki D.,Nomura S.,Fujita T.,Omata Y.,Yasui T.,Hirose J.,Matsumoto T.,Saito T.,Kadono Y.,Okada H.,Miyamoto T.,Tamura T.,Aburatani H.,and Tanaka S.,2019,Cooperation of PU.1 with IRF8 and NFATc1 defines chromatin landscapes during RANKL-induced osteoclastogenesis,J.Bone Miner.Res.,34(6):1143-1154.
Kawamura Y.,Tanaka Y.,Kawamori R.,and Maeda S.,2006,Overexpression of Krüppe l-like factor 7 regulates adipocytokine gene expressions in human adipocytes and inhibits glucose-induced insulin secretion in pancreatic beta-cell line,Mol.Endocrinol.,20(4):844-856.
Li S.,Yin M.,Liu S.X.,Chen Y.,Yin Y.Q.,Liu T.X.,and Zhou J.W.,2010,Expression of ventral diencephalon-enriched genes in zebrafish,Dev.Dyn.,239(12):3368-3379.
Lin L.G.,Pang W.J.,Chen K.Y.,Wang F.,Gengler J.,Sun Y.X.,and Tong Q.,2012,Adipocyte expression of PU.1 transcription factor causes insulin resistance through upregulation of inflammatory cytokine gene expression and ROS production,Am.J.Physiol.Endocrinol.Metab.,302(12):1550-1559.
Matsumoto N.,Laub F.,Aldabe R.,Zhang W.,Ramirez F.,Yoshida T.,and Terada M.,1998,Cloning the cDNA for a new human zinc finger protein defines a group of closely related Krüppel-like transcription factors,J.Biol.Chem.,273(43):28229-28237.
Oguchi T.,Ota M.,Ito T.,Hamano H.,Arakura N.,Katsuyama Y.,Meguro A.,and Kawa S.,2015,Investigation of susceptibility genes triggering lachrymal/salivary gland lesion complications in Japanese patients with type 1 autoimmune pancreatitis,PLoS ONE,10(5):e0127078.
Rustenhoven J.,Smith A.M.,Smyth L.C.,Jansson D.,Scotter E.L.,Swanson M.E.V.,Aalderink M.,Coppieters N.,Narayan P.,Handley R.,Overall C.,Park T.I.H.,Schweder P.,Heppner P.,Curtis M.A.,Faull R.L.M.,and Dragunow M.,2018,PU.1 regulates Alzheimer's disease-associated genes in primary human microglia,Mol.Neurodegener.,13(1):44.
Schuettpelz L.G.,Gopalan P.K.,Giuste F.O.,Romine M.P.,van Os R.,and Link D.C.,2012,Krüppe l-like factor 7 overexpression suppresses hematopoietic stem and progenitor cell function,Blood,120(15):2981-2989.
Smaldone S.,Laub F.,Else C.,Dragomir C.,and Ramirez F.,2004,Identification of MoKA,a novel F-box protein that modulates Krüppel-like transcription factor 7 activity,Mol.Cell.Biol.,24(3):1058-1069.
Smith A.M.,Gibbons H.M.,Oldfield R.L.,Bergin P.M.,Mee E.W.,Faull R.L.,and Dragunow M.,2013,The transcription factor PU.1 is critical for viability and function of human brain microglia,Glia,61(6):929-942.
Tipping A.J.,Deininger M.W.,Goldman J.M.,and Melo J.V.,2003,Comparative gene expression profile of chronic myeloid leukemia cells innately resistant to imatinib mesylate,Exp.Hematol.,31(11):1073-1080.
Vangala R.K.,Heiss-Neumann M.S.,Rangatia J.S.,Singh S.M.,Schoch C.,Tenen D.G.,Hiddemann W.,and Behre G.,2003,The myeloid master regulator transcription factor PU.1is inactivated by AML1-ETO in t (8;21) myeloid leukemia,Blood,101(1):270-277.
Wang F.,and Tong Q.,2008,Transcription factor PU.1 is expressed in white adipose and inhibits adipocyte differentiation,Am.J.Physiol.Cell Physiol.,295(1):213-220.
Wang X.,Shen Q.W.,Wang J.,Zhang Z.G.,Feng F.,Chen T.,Zhang Y.Y.,Wei H.,Li Z.W.,Wang X.X.,and Wang Y.Z.,2016,KLF7 regulates satellite cell quiescence in response to extracellular signaling,Stem Cells,34(5):1310-1320.
Wei R.,Dhawan P.,Baiocchi R.A.,Kim K.Y.,and Christakos S.,2019,PU.1 and epigenetic signals modulate 1,25-dihydroxyvitamin D3 and C/EBPalpha regulation of the human cathelicidin antimicrobial peptide gene in lung epithelial cells,J.Cell.Physiol.,234(7):10345-10359.
Xu Y.Z.,Gu S.,Bi Y.K.,Qi X.Q.,Yan Y.J.,and Lou M.Q.,2018,Transcription factor PU.1 is involved in the progression of glioma,Oncol.Lett.,15(3):3753-3759.
Zhang Z.W.,Wang H.X.,and Sun Y.N.,Li H.,and Wang N.,2013,KLF7 modulates the differentiation and proliferation of chicken preadipocyte,Acta Biochim.Biophys.Sin.,45(4):280-288.
基本信息:
DOI:10.13417/j.gab.040.001561
中图分类号:Q75
引用信息:
[1]孙婴宁,李雯,刘阔成,等.转录因子PU.1和KLF7在小鼠组织中的基因表达分析[J].基因组学与应用生物学,2021,40(04):1561-1566.DOI:10.13417/j.gab.040.001561.
基金信息:
国家自然科学基金项目(31402061); 黑龙江省基本业务专项项目(135209261); 黑龙江省省属高等学校基本科研业务费科研项目(YSTSXK201875)共同资助
2020-11-18
2020-11-18
2020-11-18