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本文引用的文献

1
Processing of X-ray diffraction data collected in oscillation mode.振荡模式下收集的X射线衍射数据的处理。
Methods Enzymol. 1997;276:307-26. doi: 10.1016/S0076-6879(97)76066-X.
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Roles of HNF-1beta in kidney development and congenital cystic diseases.肝细胞核因子-1β在肾脏发育和先天性囊性疾病中的作用。
Kidney Int. 2005 Nov;68(5):1944-7. doi: 10.1111/j.1523-1755.2005.00625.x.
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Post-crystallization treatments for improving diffraction quality of protein crystals.用于提高蛋白质晶体衍射质量的结晶后处理方法。
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Genetic and clinical characteristics of maturity-onset diabetes of the young.青年发病的成年型糖尿病的遗传和临床特征
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Mutations in hepatocyte nuclear factor-1beta and their related phenotypes.肝细胞核因子-1β的突变及其相关表型。
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Homeodomain revisited: a lesson from disease-causing mutations.再探同源结构域:致病突变带来的启示。
Hum Genet. 2005 May;116(6):433-44. doi: 10.1007/s00439-004-1252-1. Epub 2005 Feb 23.
7
Renal cysts and diabetes syndrome resulting from mutations in hepatocyte nuclear factor-1beta.由肝细胞核因子-1β突变导致的肾囊肿和糖尿病综合征。
Nephrol Dial Transplant. 2004 Nov;19(11):2703-8. doi: 10.1093/ndt/gfh348.
8
Optimum solubility (OS) screening: an efficient method to optimize buffer conditions for homogeneity and crystallization of proteins.最佳溶解度(OS)筛选:一种优化蛋白质均一性和结晶缓冲条件的有效方法。
Acta Crystallogr D Biol Crystallogr. 2004 Sep;60(Pt 9):1670-3. doi: 10.1107/S0907444904010972. Epub 2004 Aug 26.
9
Contrasting diabetes phenotypes associated with hepatocyte nuclear factor-1alpha and -1beta mutations.与肝细胞核因子-1α和-1β突变相关的不同糖尿病表型。
Diabetes Care. 2004 May;27(5):1102-7. doi: 10.2337/diacare.27.5.1102.
10
Clinical spectrum associated with hepatocyte nuclear factor-1beta mutations.与肝细胞核因子-1β突变相关的临床谱
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肝细胞核因子1β与DNA复合物的结晶。

Crystallization of hepatocyte nuclear factor 1beta in complex with DNA.

作者信息

Lu Peng, Li Yun, Gorman Amanda, Chi Young-In

机构信息

Department of Molecular and Cellular Biochemistry and Center for Structural Biology, University of Kentucky, Lexington, KY 40536, USA.

出版信息

Acta Crystallogr Sect F Struct Biol Cryst Commun. 2006 Jun 1;62(Pt 6):525-9. doi: 10.1107/S1744309106015168. Epub 2006 May 5.

DOI:10.1107/S1744309106015168
PMID:16754972
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1581457/
Abstract

Hepatocyte nuclear factor 1beta (HNF1beta) is a member of the POU transcription-factor family and binds the target DNA as a dimer with nanomolar affinity. The HNF1beta-DNA complex has been prepared and crystallized by hanging-drop vapor diffusion in 6%(v/v) PEG 300, 5%(w/v) PEG 8000, 8%(v/v) glycerol and 0.1 M Tris pH 8.0. The crystals diffracted to 3.2 A (93.9% completeness) using a synchrotron-radiation source under cryogenic (100 K) conditions and belong to space group R3, with unit-cell parameters a = b = 172.69, c = 72.43 A. A molecular-replacement solution has been obtained and structure refinement is in progress. This structure will shed light on the molecular mechanism of promoter recognition by HNF1beta and the molecular basis of the disease-causing mutations found in it.

摘要

肝细胞核因子1β(HNF1β)是POU转录因子家族的成员,以纳摩尔亲和力作为二聚体结合靶DNA。HNF1β-DNA复合物已通过悬滴气相扩散法在6%(v/v)聚乙二醇300、5%(w/v)聚乙二醇8000、8%(v/v)甘油和0.1M Tris pH 8.0中制备并结晶。使用同步辐射源在低温(100K)条件下,晶体衍射至3.2 Å(完整性为93.9%),属于R3空间群,晶胞参数a = b = 172.69,c = 72.43 Å。已获得分子置换解,结构精修正在进行中。该结构将阐明HNF1β识别启动子的分子机制以及其中发现的致病突变的分子基础。