TY - JOUR
T1 - Quantification of small non-coding RNAs allows an accurate comparison of miRNA expression profiles
AU - Masotti, Andrea
AU - Caputo, Viviana
AU - Da Sacco, Letizia
AU - Pizzuti, Antonio
AU - Dallapiccola, Bruno
AU - Bottazzo, Gian Franco
PY - 2009
Y1 - 2009
N2 - MicroRNAs (miRNAs) are highly conserved 22-mer RNA molecules, encoded by plants and animals that regulate the expression of genes binding to the 3 ′ -UTR of specific target mRNAs. The amount of miRNAs in a total RNA sample depends on the recovery efficiency that may be significantly affected by the different purification methods employed. Traditional approaches may be inefficient at recovering small RNAs, and common spectrophotometric determination is not adequate to quantify selectively these low molecular weight (LMW) species from total RNA samples. Here, we describe the use of qualitative and quantitative lab-on-a-chip tools for the analysis of these LMW RNA species. Our data emphasize the close correlation of LMW RNAs with the expression levels of some miRNAs. We therefore applied our result to the comparison of some miRNA expression profiles in different tissues. Finally, the methods we used in this paper allowed us to analyze the efficiency of extraction protocols, to study the small (but significant) differences among various preparations and to allow a proper comparison of some miRNA expression profiles in various tissues.
AB - MicroRNAs (miRNAs) are highly conserved 22-mer RNA molecules, encoded by plants and animals that regulate the expression of genes binding to the 3 ′ -UTR of specific target mRNAs. The amount of miRNAs in a total RNA sample depends on the recovery efficiency that may be significantly affected by the different purification methods employed. Traditional approaches may be inefficient at recovering small RNAs, and common spectrophotometric determination is not adequate to quantify selectively these low molecular weight (LMW) species from total RNA samples. Here, we describe the use of qualitative and quantitative lab-on-a-chip tools for the analysis of these LMW RNA species. Our data emphasize the close correlation of LMW RNAs with the expression levels of some miRNAs. We therefore applied our result to the comparison of some miRNA expression profiles in different tissues. Finally, the methods we used in this paper allowed us to analyze the efficiency of extraction protocols, to study the small (but significant) differences among various preparations and to allow a proper comparison of some miRNA expression profiles in various tissues.
UR - http://www.scopus.com/inward/record.url?scp=70349257339&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=70349257339&partnerID=8YFLogxK
U2 - 10.1155/2009/659028
DO - 10.1155/2009/659028
M3 - Article
C2 - 19727414
AN - SCOPUS:70349257339
SN - 1110-7243
VL - 2009
JO - Journal of Biomedicine and Biotechnology
JF - Journal of Biomedicine and Biotechnology
M1 - 659028
ER -