首站-论文投稿智能助手
典型文献
nr0b1(DAX1)loss of function in zebrafish causes hypothalamic defects via abnormal progenitor proliferation and differentiation
文献摘要:
The nuclear receptor DAX-1,encoded by the NR0B1 gene,is presented in the hypothalamic tissues in humans and other vertebrates.Human patients with NR0B1 mutations often have hypothalamic-pituitary defects,but the involvement of NR0B1 in hypothalamic development and function is not well under-stood.Here,we report the disruption of the nr0b1 gene in zebrafish causes abnormal expression of go-nadotropins,a reduction in fertilization rate,and an increase in postfasting food intake,which are indicators of abnormal hypothalamic functions.We find that loss of nr0b1 increases the number of prodynorphin(ppdyn)-expressing neurons but decreases the number of pro-opiomelanocortin(pomcb)-expressing neu-rons in the zebrafish hypothalamic arcuate region(ARC).Further examination reveals that the proliferation of progenitor cells is reduced in the hypothalamus of nr0b1 mutant embryos accompanying the decreased expression of genes in the Notch signaling pathway.Additionally,the inhibition of Notch signaling in wild-type embryos increases the number of pdyn neurons,mimicking the nr0b1 mutant phenotype.In contrast,ectopic activation of Notch signaling in nr0b1 mutant embryos decreases the number of pdyn neurons.Taken together,our results suggest that nr0b1 regulates neural progenitor proliferation and maintenance to ensure normal hypothalamic neuron development.
文献关键词:
作者姓名:
Wei Zhang;Yan Li;Sijie Chen;Cuizhen Zhang;Lili Chen;Gang Peng
作者机构:
State Key Laboratory of Medical Neurobiology,MOE Frontiers Center for Brain Science,Institutes of Brain Science,Fudan University,Shanghai 200032,China;Department of Endocrinology,Huashan Hospital,Fudan University,Shanghai 200040,China
文献出处:
引用格式:
[1]Wei Zhang;Yan Li;Sijie Chen;Cuizhen Zhang;Lili Chen;Gang Peng-.nr0b1(DAX1)loss of function in zebrafish causes hypothalamic defects via abnormal progenitor proliferation and differentiation)[J].遗传学报,2022(03):217-229
A类:
nr0b1,DAX1,nadotropins,postfasting,prodynorphin,ppdyn,pomcb,pdyn
B类:
loss,zebrafish,causes,hypothalamic,defects,via,abnormal,progenitor,proliferation,differentiation,nuclear,receptor,encoded,by,NR0B1,presented,tissues,humans,other,vertebrates,Human,patients,mutations,often,have,pituitary,but,involvement,development,well,under,stood,Here,report,disruption,expression,go,reduction,fertilization,food,intake,which,are,indicators,functions,We,find,that,increases,number,expressing,neurons,decreases,opiomelanocortin,arcuate,region,ARC,Further,examination,reveals,cells,reduced,hypothalamus,mutant,embryos,accompanying,decreased,genes,Notch,signaling,pathway,Additionally,inhibition,wild,mimicking,phenotype,In,contrast,ectopic,activation,Taken,together,our,results,suggest,regulates,neural,maintenance,ensure
AB值:
0.444472
相似文献
Changes in progenitors and differentiated epithelial cells of neonatal piglets
Lanmei Yin;Jun Li;Yitong Zhang;Qing Yang;Cuiyan Yang;Zhenfeng Yi;Yuebang Yin;Qiye Wang;Jianzhong Li;Nengshui Ding;Zhigang Zhang;Huansheng Yang;Yulong Yin-Hunan International Joint Laboratory of Animal Intestinal Ecology and Health,Laboratory of Animal Nutrition and Human Health,College of Life Sciences,Hunan Normal University,Changsha,Hunan,410081,China;Hunan Provincial Key Laboratory of Animal Nutritional Physiology and Metabolic Process,Scientific Observing and Experimental Station of Animal Nutrition and Feed Science in South-Central,Ministry of Agriculture,Hunan Provincial Engineering Research Center for Healthy Livestock and Poultry Production,Key Laboratory of Agro-ecological Processes in Subtropical Region,Institute of Subtropical Agriculture,Chinese Academy of Sciences,Changsha,Hunan,410125,China;National Center of Technology Innovation for Synthetic Biology,Tianjin Institute of Industrial Biotechnology,Chinese Academy of Sciences,Tianjin,300308,China;State Key Laboratory of Food Safety Technology for Meat Products,Yinxiang Group,Fujian Aonong Biological Science and Technology Group Co.,Ltd.,Key Laboratory of Swine Nutrition and Feed Science of Fujian Province,Aonong Group,Zhangzhou,Fujian,363000,China
Characterization of wavy root 1,an agravitropism allele,reveals the functions of OsPIN2 in fine regulation of auxin transport and distribution and in ABA biosynthesis and response in rice(Oryza sativa L.)
Wenqiang Li;Minjuan Zhang;Lei Qiao;Yunbo Chen;Dapeng Zhang;Xiuqing Jing;Pengfei Gan;Yangbin Huang;Junru Gao;Wenting Liu;Chunhai Shi;Hongchang Cui;Haifeng Li;Kunming Chen-State Key Laboratory of Crop Stress Biology in Arid Areas,College of Life Sciences,Northwest A&F University,Yangling 712100,Shaanxi,China;The Sericultural and Silk Research Institute,College of Animal Science and Technology,Northwest A&F University,Yangling 712100,Shaanxi,China;College of Agronomy,Northwest A&F University,Yangling 712100,Shaanxi,China;Department of Agronomy,College of Agriculture and Biotechnology,Zhejiang University,Hangzhou 310058,Zhejiang,China;Department of Biological Science,Florida State University,Tallahassee,FL 32306,USA
Spinal cord injury reprograms muscle fibroadipogenic progenitors to form heterotopic bones within muscles
Hsu-Wen Tseng;Dorothée Girard;Kylie A.Alexander;Susan M.Millard;Frédéric Torossian;Adrienne Anginot;Whitney Fleming;Jules Gueguen;Marie-Emmanuelle Goriot;Denis Clay;Beulah Jose;Bianca Nowlan;Allison R.Pettit;Marjorie Salga;Fra?ois Genêt;Marie-Carline Le Bousse-Kerdilès;Sébastien Banzet;Jean-Pierre Lévesque-Mater Research Institute—The University of Queensland,Woolloongabba,QLD,Australia;Institut de Recherche Biomédicale des Armées(IRBA),INSERM UMRS-MD,1197 Clamart,France;INSERM UMRS-MD 1197,Université de Paris-Saclay,H?pital Paul Brousse,Villejuif ,France;INSERM UMS-44,Université de Paris-Saclay,H?pital Paul Brousse,Villejuif,France;UPOH(Unité Péri Opératoire du Handicap,Perioperative Disability Unit),Physical and Rehabilitation Medicine department,Raymond-Poincaré Hospital,Assistance Publique-H?pitaux de Paris(AP-HP),Garches,France;Université de Versailles Saint Quentin en Yvelines,UFR Simone Veil-Santé,END:ICAP INSERM U1179,Montigny le Bretonneux,France
Treatment of autosomal recessive hearing loss via in vivo CRISPR/Cas9-mediated optimized homology-directed repair in mice
Xi Gu;Xinde Hu;Daqi Wang;Zhijiao Xu;Fang Wang;Di Li;Geng-lin Li;Hui Yang;Huawei Li;Erwei Zuo;Yilai Shu-ENT institute and Department of Otorhinolaryngology,Eye & ENT Hospital,State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science,Fudan University,Shanghai,China;Institutes of Biomedical Sciences,Fudan University,Shanghai,China;Department of Otolaryngology,the First Affiliated Hospital of Fujian Medical University,Fuzhou,China;NHC Key Laboratory of Hearing Medicine(Fudan University),Shanghai,China;Institute of Neuroscience,State Key Laboratory of Neuroscience,Key Laboratory of Primate Neurobiology,CAS Center for Excellence in Brain Science and Intelligence Technology,Shanghai Research Center for Brain Science and Brain-Inspired Intelligence,Shanghai Institutes for Biological Sciences,Chinese Academy of Sciences,Shanghai,China;State Key Lab for Conservation and Utilization of Subtropical Agric-Biological Resources,Guangxi University,Nanning,China;Shenzhen Branch,Guangdong Laboratory for Lingnan Modern Agriculture,Genome Analysis Laboratory of the Ministry of Agriculture,Agricultural Genomics Institute at Shenzhen,Chinese Academy of Agricultural Sciences,Shenzhen,China;The Institutes of Brain Science and the Collaborative Innovation Center for Brain Science,Fudan University,Shanghai,China
机标中图分类号,由域田数据科技根据网络公开资料自动分析生成,仅供学习研究参考。