Motivation: MicroRNAs are small (19-24 nt) noncoding RNAs that play an important role in the regulation of
multiple cell events, inhibiting gene expression at the posttranscriptional level by binding target mRNAs that
are subsequently degraded or sequestered from translation. Plant microRNA genes are typically transcribed
by Pol II to yield polyadenylated primary miRNAs (pri-miRNA). These undergo nuclear cleavage to produce
to a stem loop intermediate (pre-miRNA) with specific thermodinamic features. Further processing yields a
miRNA:miRNA* duplex with 2 nt 3\u2019 overhangs that enters a cytoplasmic ribonucleprotein complex which
mediates interaction with target mRNAs.
Systematic analyses of micro RNAs and their expression patterns have been performed in only a few plant
model species. The availability of the complete genome sequence of the grapevine (Vitis vinifera), has
already permitted genome-wide predictions of microRNAs by purely computational methods. Here we
present a comprehensive analysis of expression of both mature microRNAs and their primary transcripts in
the grapevine using oligonucleotide arrays and next generation sequencing technologies.
Methods: We integrate tanscriptome information derived from high-throughput Illumina SOLEXA and ABI
SOLiD sequence tags derived from both polyA+ transcripts and isolated small RNAs with oligonucleotide
array data. We are thus able to detect both mature microRNAs and to establish whether genomic loci
corresponding to the pre-miRNA are expressed in various tissues.
Results: Using \u201cnext generation\u201d sequencing technologies and oligonucleotide arrays, we are able to
demonstrate tissue specificity of expression of many microRNA genes and their precursor sequences. In
many cases, the unambiguous alignment of sequence tags derived from polyA+ RNA to the genomic
sequence allow provisional mapping of primary microRNA transcripts. It is hoped that the approach outlined
here will ultimately provide insights into the regulation of processing of primary microRNAs and precursor
microRNAs as well as facilitating identification of sequence elements involved in the regulation of
transcription of microRNA genes