基本信息

刘飞  男    中国科学院水生生物研究所
电子邮件: liufei2018@ihb.ac.cn
通信地址: 湖北省武汉市武昌区东湖南路7号中科院水生所2号楼913
邮政编码:430072

研究方向

1. RNA在鱼类组织器官发育和再生中的作用与机制

以斑马鱼、青鳉等模式生物为研究对象,探索MicroRNALncRNARNA结合蛋白等在大脑、性腺、眼、血液等组织器官的发育和再生中的表达动态、相互作用和调控机制,为理解人类疾病或指导遗传育种提供理论依据。

 

2. 感光系统与光周期调控鱼类行为的机制与应用

自然光的昼夜和季节性变化(光周期)指导绝大部分鱼类的生长和繁殖行为。感光系统(眼、松果体等)在监测日照和季节变化中发挥重要作用。在鱼类中,感光系统参与形成昼夜和季节性节律、协调各个器官做出相应反应的分子机制还不完全清楚。以斑马鱼、黄鳝等为模型,通过模拟光周期的变化,结合多组学的研究手段,揭示“光信号-感应细胞-循环系统-效应细胞-个体行为”中缺失的环节,为物种驯化和渔业生产提供理论基础和探索方向。


招生信息

   
招生专业
071007-遗传学
090801-水产养殖
071008-发育生物学
招生方向
鱼类性别分化与遗传育种
鱼类RNA生物学
视觉与光周期

教育背景

2010-09--2014-12   华中科技大学   博士,理学博士
2009-09--2010-06   华中科技大学   硕士(硕博连读)
2005-09--2009-06   华中科技大学   本科,理学学士

工作经历

2014-12~2021-05,华中科技大学, 博士后

2021-05~至今,中国科学院水生生物研究所, 副研究员


出版信息

   
发表论文
[1] Gao, Pan, Jia, Danna, Li, Pei, Huang, Yuwen, Hualei, Hu, Sun, Kui, Lv, Yuexia, Chen, Xiang, Han, Yunqiao, Zhang, Zuxiao, Ren, Xiang, Wang, Qing, Liu, Fei, Tang, Zhaohui, Liu, Mugen. Accumulation of Lipid Droplets in a Novel Bietti Crystalline Dystrophy Zebrafish Model With Impaired PPARalpha Pathway. INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE[J]. 2022, 63(5): 32-, https://iovs.arvojournals.org/article.aspx?articleid=2778864.
[2] Xing Lin, Fei Liu, Kaifeng Meng, Hairong Liu, Yuanli Zhao, Yuanyuan Chen, Wei Hu, Daji Luo, Einar Ring. Comprehensive Transcriptome Analysis Reveals Sex-Specific Alternative Splicing Events in Zebrafish Gonads. LIFE[J]. 2022, 12(9): https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9501657/.
[3] Liu, Fei, Qin, Yayun, Huang, Yuwen, Gao, Pan, Li, Jingzhen, Yu, Shanshan, Jia, Danna, Chen, Xiang, Lv, Yuexia, Tu, Jiayi, Sun, Kui, Han, Yunqiao, Reilly, James, Shu, Xinhua, Lu, Qunwei, Tang, Zhaohui, Xu, Chengqi, Luo, Daji, Liu, Mugen. Rod genesis driven by mafba in an nrl knockout zebrafish model with altered photoreceptor composition and progressive retinal degeneration. PLOS GENETICS[J]. 2022, 18(3): https://doaj.org/article/5ec87f08a1f5433195e0b9eaee7ac910.
[4] Danna Jia, Pan Gao, Yuexia Lv, Yuwen Huang, James Reilly, Kui Sun, Yunqiao Han, Hualei Hu, Xiang Chen, Zuxiao Zhang, Pei Li, Jiong Luo, Xinhua Shu, Zhaohui Tang, Fei Liu, Mugen Liu, Xiang Ren. Tulp1 deficiency causes early-onset retinal degeneration through affecting ciliogenesis and activating ferroptosis in zebrafish. CELL DEATH & DISEASE. 2022, 13(11): https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9672332/.
[5] Zhao, Yuanli, Chen, Kuangxin, Liu, Fei, Jiang, Mouyan, Chen, Zonggui, Chen, Huijie, Song, Yanlong, Tao, Binbin, Cui, Xuefan, Li, Yongming, Zhu, Zuoyan, Chen, Ji, Hu, Wei, Luo, Daji. Dynamic Gene Expression and Alternative Splicing Events Demonstrate Co-Regulation of Testicular Differentiation and Maturation by the Brain and Gonad in Common Carp. FRONTIERS IN ENDOCRINOLOGY[J]. 2022, 12: http://dx.doi.org/10.3389/fendo.2021.820463.
[6] Chen, Huijie, Zhao, Yuanli, Chen, Kuangxin, Wei, Yulai, Luo, Hongrui, Li, Yongming, Liu, Fei, Zhu, Zuoyan, Hu, Wei, Luo, Daji. Isolation, Identification, and Investigation of Pathogenic Bacteria From Common Carp (Cyprinus carpio) Naturally Infected With Plesiomonas shigelloides. FRONTIERS IN IMMUNOLOGY[J]. 2022, 13: http://dx.doi.org/10.3389/fimmu.2022.872896.
[7] Meng, Kaifeng, Lin, Xing, Liu, Hairong, Chen, Huijie, Liu, Fei, Xu, Zhen, Sun, Yonghua, Luo, Daji. Gonadal bacterial community composition is associated with sex-specific differences in swamp eels (Monopterus albus). FRONTIERS IN IMMUNOLOGY[J]. 2022, 13: http://dx.doi.org/10.3389/fimmu.2022.938326.
[8] Li, Jingzhen, Liu, Fei, Lv, Yuexia, Sun, Kui, Zhao, Yuntong, Reilly, Jamas, Zhang, Yangjun, Tu, Jiayi, Yu, Shanshan, Liu, Xiliang, Qin, Yayun, Huang, Yuwen, Gao, Pan, Jia, Danna, Chen, Xiang, Han, Yunqiao, Shu, Xinhua, Luo, Daji, Tang, Zhaohui, Liu, Mugen. Prpf31 is essential for the survival and differentiation of retinal progenitor cells by modulating alternative splicing. NUCLEIC ACIDS RESEARCH[J]. 2021, 49(4): 2027-2043, https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7913766/.
[9] Qin, Yayun, Gao, Pang, Yu, Shanshan, Li, Jingzhen, Huang, Yuwen, Jia, Danna, Tang, Zhaohui, Li, Pengcheng, Liu, Fei, Liu, Mugen. A large deletion spanning PITX2 and PANCR in a Chinese family with Axenfeld-Rieger syndrome. MOLECULAR VISION[J]. 2020, 26: 670-678, https://www.webofscience.com/wos/woscc/full-record/WOS:000575379500001.
[10] Tu, Jiayi, Liu, Xiliang, Jia, Haibo, Reilly, James, Yu, Shanshan, Cai, Chen, Liu, Fei, Lv, Yuexia, Huang, Yuwen, Lu, Zhaojing, Han, Shanshan, Jiang, Tao, Shu, Xinhua, Wu, Xiaoyan, Tang, Zhaohui, Lu, Qunwei, Liu, Mugen. The chromatin remodeler Brg1 is required for formation and maintenance of hematopoietic stem cells. FASEB JOURNAL[J]. 2020, 34(9): 11997-12008, https://www.webofscience.com/wos/woscc/full-record/WOS:000560233000001.
[11] Yu, Shanshan, Jiang, Tao, Jia, Danna, Han, Yundiao, Liu, Fei, Huang, Yuwen, Qu, Zhen, Zhao, Yuntong, Tu, Jiayi, Lv, Yuexia, Li, Jingzhen, Hu, Xuebin, Lu, Zhaojing, Han, Shanshan, Qin, Yayun, Liu, Xiliang, Xie, Shanglun, Wang, Qing K, Tang, Zhaohui, Luo, Daji, Liu, Mugen. BCAS2 is essential for hematopoietic stem and progenitor cell maintenance during zebrafish embryogenesis. BLOOD[J]. 2019, 133(8): 805-815, http://dx.doi.org/10.1182/blood-2018-09-876599.
[12] Xie, Shanglun, Han, Shanshan, Qu, Zhen, Liu, Fei, Li, Jingzhen, Yu, Shanshan, Reilly, James, Tu, Jiayi, Liu, Xiliang, Lu, Zhaojing, Hu, Xuebin, Yimer, Tinsae Assefa, Qin, Yayun, Huang, Yuwen, Lv, Yuexia, Jiang, Tao, Shu, Xinhua, Tang, Zhaohui, Jia, Haibo, Wong, Fulton, Liu, Mugen. Knockout of Nr2e3 prevents rod photoreceptor differentiation and leads to selective L-/M-cone photoreceptor degeneration in zebrafish. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE[J]. 2019, 1865(6): 1273-1283, http://dx.doi.org/10.1016/j.bbadis.2019.01.022.
[13] Qu, Zhen, Yimer, Tinsae Assefa, Xie, Shanglun, Wong, Fulton, Yu, Shanshan, Liu, Xiliang, Han, Shanshan, Ma, Juanjuan, Lu, Zhaojing, Hu, Xuebin, Qin, Yayun, Huang, Yuwen, Lv, Yuexia, Li, Jingzhen, Tang, Zhaohui, Liu, Fei, Liu, Mugen. Knocking out lca5 in zebrafish causes cone-rod dystrophy due to impaired outer segment protein trafficking. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE[J]. 2019, 1865(10): 2694-2705, http://dx.doi.org/10.1016/j.bbadis.2019.07.009.
[14] Hu, Xuebin, Lu, Zhaojing, Yu, Shanshan, Reilly, James, Liu, Fei, Jia, Danna, Qin, Yayun, Han, Shanshan, Liu, Xiliang, Qu, Zhen, Lv, Yuexia, Li, Jingzhen, Huang, Yuwen, Jiang, Tao, Jia, Haibo, Wang, Qing, Liu, Jingyu, Shu, Xinhua, Tang, Zhaohui, Liu, Mugen. CERKL regulates autophagy via the NAD-dependent deacetylase SIRT1. AUTOPHAGY[J]. 2019, 15(3): 453-465, [15] Lu, Zhaojing, Hu, Xuebin, Reilly, James, Jia, Danna, Liu, Fei, Yu, Shanshan, Liu, Xiliang, Xie, Shanglun, Qu, Zhen, Qin, Yayun, Huang, Yuwen, Lv, Yuexia, Li, Jingzhen, Gao, Pan, Wong, Fulton, Shu, Xinhua, Tang, Zhaohui, Liu, Mugen. Deletion of the transmembrane protein Prom1b in zebrafish disrupts outer-segment morphogenesis and causes photoreceptor degeneration. JOURNAL OF BIOLOGICAL CHEMISTRY[J]. 2019, 294(38): 13953-13963, http://dx.doi.org/10.1074/jbc.RA119.008618.
[16] Han, Shanshan, Liu, Xiliang, Xie, Shanglun, Gao, Meng, Liu, Fei, Yu, Shanshan, Sun, Peng, Wang, Changquan, Archacki, Stephen, Lu, Zhaojing, Hu, Xuebin, Qin, Yayun, Qu, Zhen, Huang, Yuwen, Lv, Yuexia, Tu, Jiayi, Li, Jingzhen, Yimer, Tinsae Assefa, Jiang, Tao, Tang, Zhaohui, Luo, Daji, Chen, Fangyi, Liu, Mugen. Knockout of ush2a gene in zebrafish causes hearing impairment and late onset rod-cone dystrophy. HUMAN GENETICS[J]. 2018, 137(10): 779-794, http://dx.doi.org/10.1007/s00439-018-1936-6.
[17] Liu, Fei, Qin, Yayun, Yu, Shanshan, Soares, Dinesh C, Yang, Lifang, Weng, Jun, Li, Chang, Gao, Meng, Lu, Zhaojing, Hu, Xuebin, Liu, Xiliang, Jiang, Tao, Liu, Jing Yu, Shu, Xinhua, Tang, Zhaohui, Liu, Mugen. Pathogenic mutations in retinitis pigmentosa 2 predominantly result in loss of RP2 protein stability in humans and zebrafish. JOURNAL OF BIOLOGICAL CHEMISTRY[J]. 2017, 292(15): 6225-6239, http://dx.doi.org/10.1074/jbc.M116.760314.
[18] Lu, Zhaojing, Hu, Xuebin, Liu, Fei, Soares, Dinesh C, Liu, Xiliang, Yu, Shanshan, Gao, Meng, Han, Shanshan, Qin, Yayun, Li, Chang, Jiang, Tao, Luo, Daji, Guo, AnYuan, Tang, Zhaohui, Liu, Mugen. Ablation of EYS in zebrafish causes mislocalisation of outer segment proteins, F-actin disruption and cone-rod dystrophy. SCIENTIFIC REPORTS[J]. 2017, 7: https://www.webofscience.com/wos/woscc/full-record/WOS:000398396700002.
[19] Qin, Y, Liu, F, Yu, S, Yang, L, Gao, M, Tang, Z, Guo, A Y, Zhang, M, Li, P, Liu, M. Identification of a novel NRL mutation in a Chinese family with retinitis pigmentosa by whole-exome sequencing. EYEnull. 2017, 31(5): 815-817, https://www.webofscience.com/wos/woscc/full-record/WOS:000401036900026.
[20] Gao, Meng, Huang, Yuwen, Wang, Ling, Huang, Mi, Liu, Fei, Liao, Shengjie, Yu, Shanshan, Lu, Zhaojing, Han, Shanshan, Hu, Xuebin, Qu, Zhen, Liu, Xiliang, Yimer, Tinsae Assefa, Yang, Lifang, Tang, Zhaohui, Li, David WanCheng, Liu, Mugen. HSF4 regulates lens fiber cell differentiation by activating p53 and its downstream regulators. CELL DEATH & DISEASE[J]. 2017, 8: https://www.webofscience.com/wos/woscc/full-record/WOS:000414022900077.
[21] Raghupathy, Rakesh K, Zhang, Xun, Liu, Fei, Alhasani, Reem H, Biswas, Lincoln, Akhtar, Saeed, Pan, Luyuan, Moens, Cecilia B, Li, Wenchang, Liu, Mugen, Kennedy, Breandan N, Shu, Xinhua. Rpgrip1 is required for rod outer segment development and ciliary protein trafficking in zebrafish. SCIENTIFIC REPORTS[J]. 2017, 7(1): https://doaj.org/article/602eddd565b94b33be91305ae1cba6cc.
[22] Yu, Shanshan, Li, Chang, Biswas, Lincoln, Hu, Xuebin, Liu, Fei, Reilly, James, Liu, Xiliang, Liu, Ying, Huang, Yuwen, Lu, Zhaojing, Han, Shanshan, Wang, Lei, Liu, Jing Yu, Jiang, Tao, Shu, Xinhua, Wong, Fulton, Tang, Zhaohui, Liu, Mugen. CERKL gene knockout disturbs photoreceptor outer segment phagocytosis and causes rod-cone dystrophy in zebrafish. HUMAN MOLECULAR GENETICS[J]. 2017, 26(12): 2335-2345, http://dx.doi.org/10.1093/hmg/ddx137.
[23] Gao, Meng, Zhang, Su, Liu, Chunjie, Qin, Yayun, Archacki, Stephen, Jin, Ling, Wang, Yong, Liu, Fei, Chen, Jiaxiang, Liu, Ying, Wang, Jiuxiang, Huang, Mi, Liao, Shengjie, Tang, Zhaohui, Guo, An Yuan, Jiang, Fagang, Liu, Mugen. Whole exome sequencing identifies a novel NRL mutation in a Chinese family with autosomal dominant retinitis pigmentosa. MOLECULAR VISION[J]. 2016, 22: 234-242, https://www.webofscience.com/wos/woscc/full-record/WOS:000373453400001.
[24] Wang, Jiuxiang, Liu, Ying, Liu, Fei, Huang, Changzheng, Han, Shanshan, Lv, Yuexia, Liu, ChunJie, Zhang, Su, Qin, Yayun, Ling, Lei, Gao, Meng, Yu, Shanshan, Li, Chang, Huang, Mi, Liao, Shengjie, Hu, Xuebin, Lu, Zhaojing, Liu, Xiliang, Jiang, Tao, Tang, Zhaohui, Zhang, Huiping, Guo, AnYuan, Liu, Mugen. Loss-of-function Mutation in PMVK Causes Autosomal Dominant Disseminated Superficial Porokeratosis. SCIENTIFIC REPORTS[J]. 2016, 6: https://www.webofscience.com/wos/woscc/full-record/WOS:000373580100001.
[25] Liu, Fei, Chen, Jiaxiang, Yu, Shanshan, Raghupathy, Rakesh Kotapati, Liu, Xiliang, Qin, Yayun, Li, Chang, Huang, Mi, Liao, Shengjie, Wang, Jiuxiang, Zou, Jian, Shu, Xinhua, Tang, Zhaohui, Liu, Mugen. Knockout of RP2 decreases GRK1 and rod transducin subunits and leads to photoreceptor degeneration in zebrafish. HUMAN MOLECULAR GENETICS[J]. 2015, 24(16): 4648-4659, http://dx.doi.org/10.1093/hmg/ddv197.
[26] Mi Huang, Duanzhuo Li, Yuwen Huang, Xiukun Cui, Shengjie Liao, Jiuxiang Wang, Fei Liu, Chang Li, Meng Gao, Jiaxiang Chen, Zhaohui Tang, David Wan-Cheng Li, Mugen Liu. HSF4 promotes G1/S arrest in human lens epithelial cells by stabilizing p53. BBA - MOLECULAR CELL RESEARCH. 2015, 1853(8): 1808-1817, http://dx.doi.org/10.1016/j.bbamcr.2015.04.018.
[27] Chen, Jiaxiang, Liu, Fei, Li, Hui, Archacld, Stephen, Gao, Meng, Liu, Ying, Liao, Shengjie, Huang, Mi, Wang, Jiuxiang, Yu, Shanshan, Li, Chang, Tang, Zhaohui, Liu, Mugen. pVHL interacts with Ceramide kinase like (CERKL) protein and ubiquitinates it for oxygen dependent proteasomal degradation. CELLULAR SIGNALLING[J]. 2015, 27(11): 2314-2323, http://dx.doi.org/10.1016/j.cellsig.2015.08.011.
[28] Liao, Shengjie, Du, Rong, Wang, Lei, Qu, Zhen, Cui, Xiukun, Li, Chang, Liu, Fei, Huang, Mi, Wang, Jiuxiang, Chen, Jiaxiang, Gao, Meng, Yu, Shanshan, Tang, Zhaohui, Li, David WanCheng, Jiang, Tao, Liu, Mugen. BCAS2 interacts with HSF4 and negatively regulates its protein stability via ubiquitination. INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY[J]. 2015, 68: 78-86, http://dx.doi.org/10.1016/j.biocel.2015.08.016.
[29] Zhang, J, Cui, X, Wang, L, Liu, F, Jiang, T, Li, C, Li, D, Huang, M, Liao, S, Wang, J, Chen, J, Jia, H, He, J, Tang, Z, Yin, Z, Liu, M. The Mitochondrial Thioredoxin is Required for Liver Development in Zebrafish. CURRENT MOLECULAR MEDICINE[J]. 2014, 14(6): 772-782, http://www.irgrid.ac.cn/handle/1471x/929278.
[30] Liu, Fei, Huang, Yinghao, Liu, Luying, Liang, Bo, Qu, Zhen, Huang, Gang, Li, Chang, Tian, Ronghua, Jiang, Zhuhui, Liu, Fucan, Yu, Xiaoyan, Huang, Yingjie, Liu, Jingyu, Tang, Zhaohui. Identification of a novel NOG mutation in a Chinese family with proximal symphalangism. CLINICA CHIMICA ACTA[J]. 2014, 429: 129-133, http://dx.doi.org/10.1016/j.cca.2013.12.004.
[31] Chang Li, Lei Wang, Jing Zhang, Mi Huang, Fulton Wong, Xuexue Liu, Fei Liu, Xiukun Cui, Guohua Yang, Jiaxiang Chen, Ying Liu, Jiuxiang Wang, Shengjie Liao, Meng Gao, Xuebin Hu, Xinhua Shu, Qing Wang, Zhan Yin, Zhaohui Tang, Mugen Liu. CERKL interacts with mitochondrial TRX2 and protects retinal cells from oxidative stress-induced apoptosis. BBA - MOLECULAR BASIS OF DISEASE. 2014, 1842(7): 1121-1129, http://dx.doi.org/10.1016/j.bbadis.2014.04.009.
[32] Liu, Fei, Li, Pengcheng, Liu, Ying, Li, Weirong, Wong, Fulton, Du, Rong, Wang, Lei, Li, Chang, Jiang, Fagang, Tang, Zhaohui, Liu, Mugen. Novel compound heterozygous mutations in MYO7A in a Chinese family with Usher syndrome type 1. MOLECULAR VISION[J]. 2013, 19: 695-701, https://www.webofscience.com/wos/woscc/full-record/WOS:000316417500006.
[33] Qiufen Wang, Fei Liu, Yue Xing, Xianjin Wei, Hui Li, Shirong Zhang, Jingyu Liu, Qing Wang, Zhaohui Tang, Mugen Liu. Mutation c.359_363delGTATTinsATAC in the COL4A5 Causes alport syndrome in a Chinese family. GENE. 2013, 512(2): 482-485, http://dx.doi.org/10.1016/j.gene.2012.10.014.

科研活动

2015.10-2016.12 中国博士后科学基金面上项目,RP2敲除下调RAP1GDS1的机制及其在RP发生中的意义,5万元,主持

2017.1-2019.12 国家自然科学基金青年项目,RP2突变导致其蛋白水平降低并引起视网膜色素变性的机制研究,21万元,主持

2019.1-2022.12 国家自然科学基金面上项目,剪接因子prpf31功能及其突变引起视网膜色素变性和眼发育异常的分子机制,60万元,第二参与人

2019.11-2024.10 中国科学院先导专项A, 鲤高产性状的分子基础-鲤性别控制的RNA基础,100万元,参与人


在研项目
( 1 ) 鲤高产性状的分子基础-鲤性别控制的RNA基础, 参与, 部委级, 2019-11--2024-10
( 2 ) 剪接因子prpf31功能及其突变引起视网膜色素变性和眼发育异常的分子机制, 参与, 国家级, 2019-01--2022-12