{{'Search' | translate}}
 

Glycerol (Certified ACS), Fisher Chemical

Company: Fisher Scientific
Catalog#: G33
Bio-protocol()
Company-protocol()
Other protocol()

Biochemical Analysis of Dimethyl Suberimidate-crosslinked Yeast Nucleosomes
Author:
Date:
2018-03-20
[Abstract]  Nucleosomes are the fundamental unit of eukaryotic chromosome packaging, comprised of 147 bp of DNA wrapped around two molecules of each of the core histone proteins H2A, H2B, H3, and H4. Nucleosomes are symmetrical, with one axis of symmetry centered on the homodimeric interaction between the C-termini of the H3 molecules. To explore the functional consequences of nucleosome symmetry, we designed an obligate pair of H3 heterodimers, termed H3X and H3Y, allowing us to compare cells with single or double H3 alterations. Our biochemical validation of the heterodimeric X-Y interaction included intra-nucleosomal H3 crosslinking using dimethyl suberimidate (DMS). Here, we provide a detailed protocol for the use of DMS to analyze yeast nucleosomes. [摘要]  核小体是真核染色体包装的基本单元,由围绕核心组蛋白H2A,H2B,H3和H4中的每一个的两个分子包裹的147bp DNA组成。 核小体是对称的,一个对称轴以H3分子的C-末端之间的同源二聚体相互作用为中心。 为了探索核小体对称性的功能性后果,我们设计了一对特异性H3异二聚体,称为H3X和H3Y,使我们能够比较具有单一或双重H3改变的细胞。 我们对异二聚体X-Y相互作用的生物化学验证包括使用二甲基琥珀三酸酯(DMS)进行的核内H3交联。 在这里,我们提供了使用DMS来分析酵母核小体的详细方案。

【背景】组蛋白的翻译后修饰影响染色体生物学的各个方面,包括转录,复制,修复和重组。因为核小体包含每个核心组蛋白的两个拷贝,所以修饰可以是对称的(在两个H3尾部上的相同修饰,例如,在核小体内的两个H3尾部上的K27me(Voigt等人

对于单个核小体内H3X-H3Y相互作用的生化验证,我们生成了表达细菌生物素连接酶BirA,N-末端V5-标记的H3X和N-末端生物素接受表位标记的H3Y的酵母菌株(Beckett等人, 1999)。 ...

Method for Multiplexing CRISPR/Cas9 in Saccharomyces cerevisiae Using Artificial Target DNA Sequences
Author:
Date:
2017-09-20
[Abstract]  Genome manipulation has become more accessible given the advent of the CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) editing technology. The Cas9 endonuclease binds a single stranded (single guide) RNA (sgRNA) fragment that recruits the complex to a corresponding genomic target sequence where it induces a double stranded break. Eukaryotic repair systems allow for the introduction of exogenous DNA, repair of existing mutations, or deletion of endogenous gene products. Targeting of Cas9 to multiple genomic positions (termed ‘multiplexing’) is achieved by the expression of multiple sgRNAs within the same nucleus. However, an ongoing concern of the CRISPR field has been the accidental targeting of Cas9 to alternative (‘off-target’) DNA locations within a genome. We ... [摘要]  鉴于CRISPR(集群定期间隔短回归重复)编辑技术的出现,基因组操纵变得更加易于使用。 Cas9核酸内切酶将募集复合物的单链(单向导)RNA(sgRNA)片段结合到相应的基因组靶序列,引发双链断裂。真核修复系统允许引入外源DNA,修复现有突变或内源基因产物的缺失。通过在同一核内表达多个sgRNA来实现Cas9对多个基因组位置的定位(称为“多重”)。然而,CRISPR领域的持续关注是将Cas9意外地定位到基因组内的替代(“脱靶”)DNA位置。我们将安装的人造Cas9靶序列的使用(称为人造基因座上的Cas9复制)描述为允许(i)与单个sgRNA复用的酵母基因组中的用途; (ii)减少/消除可能的脱靶效应,以及(iii)精确控制预定目标序列的放置。
【背景】CRISPR(集群定期间隔回归重复)机制已经在原核生物中演变为具有很高精度编辑任何基因组的能力的原始适应性免疫系统(Jinek等,2012; Sorek等,2013)。这种生物技术需要使用来自化脓性链球菌(或othologous物种)的内切核酸酶(Cas9),单个RNA'引导'序列和外源供体DNA(如果需要)。仅在短短几年内,CRISPR / ...

Comments