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Endogenous protein marking method used for Chip-seq genome-wide binding spectrum

A genome-wide, protein labeling technology, applied in the field of protein labeling, can solve the problem of unclear transcriptional regulation mechanism of transcription factors

Inactive Publication Date: 2017-02-15
TONGJI UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

This patented method allows for better control over how different types of nucleic acid can enter living organisms by controllably deliver them inside target organs such as humans or animals without causing harmful side effects like immune responses from innate defense mechanisms. It also includes various ways to measure these properties accurately during research studies.

Problems solved by technology

This patented technical solution describes how CRIS PR/CAS plays important roles in controlling gene expression through modifying proteins involved in cellular processes such as metabolism or signal transmission. However, there remains room for improvement over current methods based solely on enzymatic activity alone without considering other aspects like regulators and drug discovery capabilities.

Method used

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  • Endogenous protein marking method used for Chip-seq genome-wide binding spectrum
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  • Endogenous protein marking method used for Chip-seq genome-wide binding spectrum

Examples

Experimental program
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Effect test

Embodiment 1

[0036] Marking of the NCOA1 gene in breast cancer cell MCF7 and its genomic transcriptional profiling. Concrete method based on the present invention is as follows:

[0037] (1) sgRNA library establishment:

[0038] Use the online design website http: / / cistrome.org / crispr / tool ​​developed by our laboratory to design sgRNA for the upstream and downstream 50bp region of the stop codon site (stop codon site) of the three ERα co-transcription factor genes, and introduce the DNA open To further screen the sgRNA located on the genomic DNA with a high degree of openness.

[0039] (2) Construction of a lentiviral vector containing sgRNA:

[0040] The sequence 5'-GACCA-3' was added to the 5' end of the sgRNA sequence, and the sequence 5'-GACCA-3' was added to the 5' end of the reverse complementary sequence of the sgRNA. Synthesize modified sgRNA sequences. The lentiviral plasmid is the lentiCRISPRv2 plasmid with Cas9 and Puro elements, such as Figure 4 shown. The lentiCRISPRv2 ...

Embodiment 2

[0054] CRISPR / Cas9 applied to the liver cancer cell line HepG2 is applied to a CRISPR / Cas9 enrichment sequencing method for large-scale screening of cancer genes, including the following steps:

[0055] (1) Design sgRNA:

[0056] Use the online design website http: / / cistrome.org / crispr / tool ​​developed by our laboratory to design sgRNA for the upstream and downstream 50bp region of the stop codon site (stop codon site) of the three ERα co-transcription factor genes, and introduce the DNA open To further screen the sgRNA located on the genomic DNA with a high degree of openness.

[0057] (2) Construction of a lentiviral vector containing sgRNA:

[0058] The sequence 5'-GACCA-3' was added to the 5' end of the sgRNA sequence, and the sequence 5'-GACCA-3' was added to the 5' end of the reverse complementary sequence of the sgRNA. Synthesize modified sgRNA sequences. The lentiCRISPRv2 plasmid with Cas9 and Puro elements was selected as the lentiviral plasmid. The lentiCRISPRv2 ...

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Abstract

The invention relates to an endogenous protein marking method applied to genome-wide binding spectrum analysis. The method comprises the steps of designing sgRNA for upstream and downstream 50bp regions of an encoding termination site of an NCOA1 gene; verifying cutting efficiency of sgRNA mediated Cas9 by an experiment; building an anti-estrogen therapy tolerant MCF-7 breast cancer cell model; by utilizing a CRISPR/Cas9 homologous recombination technology, selecting and using effective sgRNA and DNA donors, and introducing a Flag tag in the 3' end of the ER alpha co-transcription factor NCOA1 gene; and establishing a stable cell line with the Flag tag. Compared with the prior art, the method has the advantages that gene editing is performed by utilizing the CRISPR/Cas9 technology, so that the tag insertion efficiency of the gene editing is greatly improved; more importantly, chromatin structure parameters are introduced for designing sgRNA, so that effective cutting of Cas9 at a target site of a genome is ensured; and positive clone screening is performed by adopting DNA sequencing and RT-PCR sequencing methods, so that the positive clone identification step is simplified and the manpower and material resources for screening are reduced.

Description

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Claims

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Application Information

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Owner TONGJI UNIV
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