¼¼¹Ì³ª/Çà»ç

> Á¤º¸¼¾ÅÍ > ¼¼¹Ì³ª/Çà»ç

Á¦¸ñ 2019³â 11¿ù 12ÀÏ »ý¹°Á¤º¸ÇÐ ¼¼¹Ì³ª
ÀÛ¼ºÀÚ °ü¸®ÀÚ ÀÛ¼ºÀÏ 2019-11-06

¼­¿ï´ëÇб³ »ý¹°Á¤º¸ÇÐ Çùµ¿°úÁ¤ ÁÖÃÖ·Î ¼¼¹Ì³ª¸¦ ¾Æ·¡¿Í °°ÀÌ ¿­°íÀÚ ÇÏ¿À´Ï ¸¹Àº Âü¿© ¹Ù¶ø´Ï´Ù.


ÀϽÃ:¡¡¡¡2019³â 11¿ù 12ÀÏ È­¿äÀÏ ¿ÀÀü 11½Ã

¿¬»ç:¡¡ ÀåÇý½Ä ±³¼ö´Ô¡¡(¼­¿ï´ëÇб³)

Àå¼Ò:¡¡¡¡¼­¿ï´ëÇб³¡¡300µ¿ (À¯È¸Áø ÇмúÁ¤º¸°ü) 611È£


TITLE

Single-molecule RNA analysis with nanopore sequencing


ABSTRACT

¡¡The regulatory elements in RNA give rise to the specificity of the regulations that it receives. As a result, depending on the context, an RNA molecule forms different secondary structures,¡¡binds to different proteins, and gains different chemical modifications or tails. Since the introduction of RNA-Seq to the field, newly developed high-throughput techniques have driven¡¡the massive transcriptome-wide discovery of novel RNA regulations. However, two common¡¡drawbacks in the second generation sequencers have prohibited analyzing the status of¡¡regulatory sites in the broader context of the transcripts. The first problem comes from the¡¡indispensable reverse-transcription, and another is from the short read¡¡lengths. Nanopore sequencing is an entirely different approach that is free from those limitations. It reads the nucleic acid sequences by measuring ionic current changes during their¡¡migrations through a tiny hole in the middle of a transmembrane protein. This alternative¡¡strategy makes it possible to directly monitor the chemical details of the bases throughout the¡¡full lengths of RNA molecules one by one. We are carrying out examinations how nanopore direct RNA sequencing adds new dimensions of the understandings across the¡¡life cycle of RNA. In this talk, I will briefly discuss the preliminary results from our first trials, which include poly(A) tail length measurement, transcriptome timestamping, multiplexed¡¡sequencing, targeted sequencing, secondary structure probing, and base modification¡¡detection.