Evidence for Antisense Transcription Associated with MicroRNA Target mRNAs in Arabidopsis

被引:29
作者
Luo, Qing-Jun [1 ]
Samanta, Manoj P. [2 ]
Koksal, Fatih [3 ]
Janda, Jaroslav [4 ,5 ]
Galbraith, David W. [4 ,5 ]
Richardson, Casey R. [6 ]
Ou-Yang, Fangqian [1 ]
Rock, Christopher D. [1 ]
机构
[1] Texas Tech Univ, Dept Biol Sci, Lubbock, TX 79409 USA
[2] Systemix Inst, Los Altos, CA USA
[3] Texas Tech Univ, Dept Math & Stat, Lubbock, TX 79409 USA
[4] Univ Arizona, Inst BIO5, Tucson, AZ USA
[5] Univ Arizona, Dept Plant Sci, Tucson, AZ 85721 USA
[6] Texas Tech Univ, Dept Comp Sci, Lubbock, TX 79409 USA
关键词
TRANS-ACTING SIRNAS; GENE-EXPRESSION ANALYSIS; DIRECTED CLEAVAGE; PLANT MICRORNAS; HUMAN PROMOTERS; LEAF POLARITY; MIRNA TARGETS; POLYMERASE; THALIANA; GENOME;
D O I
10.1371/journal.pgen.1000457
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Antisense transcription is a pervasive phenomenon, but its source and functional significance is largely unknown. We took an expression-based approach to explore microRNA (miRNA)-related antisense transcription by computational analyses of published whole-genome tiling microarray transcriptome and deep sequencing small RNA (smRNA) data. Statistical support for greater abundance of antisense transcription signatures and smRNAs was observed for miRNA targets than for paralogous genes with no miRNA cleavage site. Antisense smRNAs were also found associated with MIRNA genes. This suggests that miRNA-associated "transitivity'' (production of small interfering RNAs through antisense transcription) is more common than previously reported. High-resolution (3 nt) custom tiling microarray transcriptome analysis was performed with probes 400 bp 59 upstream and 39 downstream of the miRNA cleavage sites (direction relative to the mRNA) for 22 select miRNA target genes. We hybridized RNAs labeled from the smRNA pathway mutants, including hen1-1, dc/1-7, hy/1-2, rdr6-15, and sgs3-14. Results showed that antisense transcripts associated with miRNA targets were mainly elevated in hen1-1 and sgs3-14 to a lesser extent, and somewhat reduced in dc/11-7, hy/11-2, or rdr6-15 mutants. This was corroborated by semi-quantitative reverse transcription PCR; however, a direct correlation of antisense transcript abundance in MIR164 gene knockouts was not observed. Our overall analysis reveals a more widespread role for miRNA-associated transitivity with implications for functions of antisense transcription in gene regulation. HEN1 and SGS3 may be links for miRNA target entry into different RNA processing pathways.
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页数:19
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