FFPEcap-seq: a method for sequencing capped RNAs in formalin-fixed paraffin-embedded samples

被引:9
|
作者
Vahrenkamp, Jeffery M. [1 ]
Szczotka, Kathryn [2 ]
Dodson, Mark K. [2 ]
Jarboe, Elke A. [3 ]
Soisson, Andrew P. [2 ]
Gertz, Jason [1 ]
机构
[1] Univ Utah, Huntsman Canc Inst, Dept Oncol Sci, Salt Lake City, UT 84112 USA
[2] Univ Utah, Huntsman Canc Inst, Dept Obstet & Gynecol, Salt Lake City, UT 84112 USA
[3] Univ Utah, Dept Pathol, Huntsman Canc Inst, Salt Lake City, UT 84112 USA
基金
美国国家卫生研究院;
关键词
TRANSCRIPTION FACTOR-BINDING; ESTROGEN-RECEPTOR-ALPHA; GENE-EXPRESSION; SINGLE-CELL; ENHANCER RNAS; CANCER; RECURRENCE; INITIATION;
D O I
10.1101/gr.249656.119
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The majority of clinical cancer specimens are preserved as formalin-fixed paraffin-embedded (FFPE) samples. For clinical molecular tests to have wide-reaching impact, they must be applicable to FFPE material. Accurate quantitative measurements of RNA derived from FFPE specimens is challenging because of low yields and high amounts of degradation. Here, we present FFPEcap-seq, a method specifically designed for sequencing capped 5' ends of RNA derived from FFPE samples. FFPEcap-seq combines enzymatic enrichment of 5' capped RNAs with template switching to create sequencing libraries. We find that FFPEcap-seq can faithfully capture mRNA expression levels in FFPE specimens while also detecting enhancer RNAs that arise from distal regulatory regions. FFPEcap-seq is a fast and straightforward method for making high-quality 5' end RNA-seq libraries from FFPE-derived RNA.
引用
收藏
页码:1826 / 1835
页数:10
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