Simultaneous Profiling of Chromatin-Associated RNA at Targeted DNA Loci and RNA-RNA Interactions through TaDRIM-Seq
ID:62 View Protection:ATTENDEE Updated Time:2024-10-27 16:53:51 Hits:1675 Invited speech

Start Time:2024-11-01 17:10(Asia/Shanghai)

Duration:20min

Session:S3 分会场三:三维基因组学技术(新技术、分析工具与AI) » S3-1分会场三:三维基因组学技术(新技术、分析工具与AI)

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Abstract
Eukaryotic genomes are extensively transcribed into various types of RNAs, many of which are physically associated with chromatin in cisat their transcription sites or in transto other genomic loci. Emerging roles have been uncovered for these chromatin-associated RNAs (caRNAs) in gene regulation and genome organization, yet they remain challenging to interrogate. Here, we present TaDRIM-seq, a technique employing Protein G (PG)-Tn5-targeted DNA elements and in situ proximity ligation to concurrently probe caRNAs across diverse genomic regions as well as global RNA-RNA interactions within intact nuclei.Notably, this approach diminishes required cell inputs, minimizes hands-on time compared to established methodologies, and is compatible in both mammalian cells and plants. Using this technique, we identified extensive caRNAs at DNA anchor regions associated with chromatin loops and revealed diurnal variation in RNA-DNA and RNA-RNA connectivity networks within rice.


Eukaryotic genomes are extensively transcribed into various types of RNAs, many of which are physically associated with chromatin in cisat their transcription sites or in transto other genomic loci. Emerging roles have been uncovered for these chromatin-associated RNAs (caRNAs) in gene regulation and genome organization, yet they remain challenging to interrogate. Here, we present TaDRIM-seq, a technique employing Protein G (PG)-Tn5-targeted DNA elements and in situ proximity ligation to concurrently probe caRNAs across diverse genomic regions as well as global RNA-RNA interactions within intact nuclei.Notably, this approach diminishes required cell inputs, minimizes hands-on time compared to established methodologies, and is compatible in both mammalian cells and plants. Using this technique, we identified extensive caRNAs at DNA anchor regions associated with chromatin loops and revealed diurnal variation in RNA-DNA and RNA-RNA connectivity networks within rice.


 
Keywords
TaDRIM-seq, Chromatin-Associated RNA, RNA-RNA interactions,DNA Elements
Speaker
李兴旺 (Xingwang Li)
华中农业大学 (Huazhong Agricultural University)

Submission Author
李兴旺 华中农业大学
丁城 华中农业大学
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Important Date
  • Conference Date

    Oct 31

    2024

    to

    Nov 03

    2024

  • Nov 03 2024

    Registration deadline

Sponsored By
崖州湾国家实验室
华中农业大学
浙江大学
中国遗传学会
中国遗传学会三维基因组学专委会
Organized By
中国生物信息学基因组信息学专委会
中国遗传学会表观遗传分会
中国细胞生物学学会染色质生物学分会
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