10月14日 Matthias Bochtler:Sensing and mapping DNA methylation(68周年校庆系列学术报告)

时间🧝🏻:2019-10-06浏览:71设置


讲座题目:Sensing and mapping DNA methylation

主讲人🙎🏼‍♀️:Matthias Bochtler  教授

主持人:翁杰敏  教授

开始时间:2019-10-14 10:00:00

讲座地址🎑:生命科学学院534小会议室

主办单位🩱🤛:生命科学学院

 

报告人简介🤳🏽:

19901992🧑🏼‍🏭:Studies in   physics at the LMU Munich

19921993Guest   student at the University of Cambridge, UK

19931995Studies in   physics at the LMU Munich. Diploma with distinction

19961999PhD at the   Max Planck Institute of Biochemistry in Martinsried (Germany) under Prof.   Robert Huber (summa cum   laude)

19992000Postdoc at   the Max Planck Institute of Biochemistry in Martinsried

2001-present🥌:Head of a joint MPG-PAN Junior Research Group at the International  Institute of Molecular and Cell Biology (IIMCB) in Warsaw

2005/2006 Habilitation in biochemistry at the   Institute of Bioorganic Chemistry (IChB) PAN in Poznan (submission 2005,   official confirmation 2006).

2007-2011👮🏽‍♀️:Head of Structural Biology, Cardiff University (United Kingdom)

2009Professorial title awarded by the President of the Republic of Poland

2011-present Group Leader at IIMCB and   professor at the Institute of Biochemistry and Biophysics (IBB) of the Polish   Academy of Sciences


报告内容🩳🧑🏼‍🦱:

Enzymatic DNA methylation comes in three main   varieties, as as 5-methylcytosine, 4-methylcytosine, and 6-methyladenine. In   the first part of my talk, I will report crystallographic and bioinformatic   data on how DNA methylation is sensed by proteins, both negatively and  positively. I will show that there is a small modular toolkit for this task,   and that cytosine and adenine methylation are detected rather differently. In   the second part of my talk, I will describe our efforts to characterize   maintenance of DNA methylation in a model organism, the plant A. thaliana, by   bisulfite conversion and reversible terminator (Illumina) sequencing, and by   Nanopore sequencing. The data indicate strong long range correlations in  methylation of a single DNA molecule, and provide evidence for crosstalk   between different methylation types (CpG, CHG, CHH)

 


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