Nascent-Seq Indicates Widespread Cotranscriptional RNA Editing in Drosophila

被引:99
作者
Rodriguez, Joseph [1 ,2 ]
Menet, Jerome S. [1 ,2 ]
Rosbash, Michael [1 ,2 ]
机构
[1] Brandeis Univ, Howard Hughes Med Inst, Natl Ctr Behav Genom, Waltham, MA 02451 USA
[2] Brandeis Univ, Dept Biol, Waltham, MA 02451 USA
基金
美国国家科学基金会;
关键词
ENZYME ADAR1; GLUR-B; MUTATION; GENE; DETERMINANTS; RETENTION; DEFICIENT; LETHALITY; EVOLUTION; ADENOSINE;
D O I
10.1016/j.molcel.2012.05.002
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 RNA editing enzyme ADAR chemically modifies adenosine (A) to inosine (I), which is interpreted by the ribosome as a guanosine. Here we assess cotranscriptional A-to-I editing in Drosophila by isolating nascent RNA from adult fly heads and subjecting samples to high throughput sequencing. There are a large number of edited sites within nascent exons. Nascent RNA from an ADAR-null strain was also sequenced, indicating that almost all A-to-I events require ADAR. Moreover, mRNA editing levels correlate with editing levels within the cognate nascent RNA sequence, indicating that the extent of editing is set cotranscriptionally. Surprisingly, the nascent data also identify an excess of intronic over exonic editing sites. These intronic sites occur preferentially within introns that are poorly spliced cotranscriptionally, suggesting a link between editing and splicing. We conclude that ADAR-mediated editing is more widespread than previously indicated and largely occurs cotranscriptionally.
引用
收藏
页码:27 / 37
页数:11
相关论文
共 39 条
[1]  
Abruzzi KC, 2011, GENE DEV, V25, P2374, DOI [10.1101/gad.178079.111, 10.1101/gad.174110.111]
[2]   AN UNWINDING ACTIVITY THAT COVALENTLY MODIFIES ITS DOUBLE-STRANDED-RNA SUBSTRATE [J].
BASS, BL ;
WEINTRAUB, H .
CELL, 1988, 55 (06) :1089-1098
[3]   Control of human potassium channel inactivation by editing of a small mRNA hairpin [J].
Bhalla, T ;
Rosenthal, JJC ;
Holmgren, M ;
Reenan, R .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2004, 11 (10) :950-956
[4]   Coordination of editing and splicing of glutamate receptor pre-mRNA [J].
Bratt, E ;
Öhman, M .
RNA, 2003, 9 (03) :309-318
[5]   EARLY-ONSET EPILEPSY AND POSTNATAL LETHALITY ASSOCIATED WITH AN EDITING-DEFICIENT GLUR-B ALLELE IN MICE [J].
BRUSA, R ;
ZIMMERMANN, F ;
KOH, DS ;
FELDMEYER, D ;
GASS, P ;
SEEBURG, PH ;
SPRENGEL, R .
SCIENCE, 1995, 270 (5242) :1677-1680
[6]   SR proteins function in coupling RNAP II transcription to pre-mRNA splicing [J].
Das, Rita ;
Yu, Jiong ;
Zhang, Zuo ;
Gygi, Melanie P. ;
Krainer, Adrian R. ;
Gygi, Steven P. ;
Reed, Robin .
MOLECULAR CELL, 2007, 26 (06) :867-881
[7]   Structure and sequence determinants required for the RNA editing of ADAR2 substrates [J].
Dawson, TR ;
Sansam, CL ;
Emeson, RB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (06) :4941-4951
[8]   SINEs point to abundant editing in the human genome [J].
DeCerbo, J ;
Carmichael, GG .
GENOME BIOLOGY, 2005, 6 (04)
[9]   Retention and repression: fates of hyperedited RNAs in the nucleus [J].
DeCerbo, J ;
Carmichael, GG .
CURRENT OPINION IN CELL BIOLOGY, 2005, 17 (03) :302-308
[10]   The RNA-editing enzyme ADAR1 is localized to the nascent ribonucleoprotein matrix on Xenopus lampbrush chromosomes but specifically associates with an atypical loop [J].
Eckmann, CR ;
Jantsch, MF .
JOURNAL OF CELL BIOLOGY, 1999, 144 (04) :603-615