Micro-RNA-like effects of complete intronic sequences

被引:23
作者
Hill, AE
Hong, JS
Wen, H
Teng, LH
McPherson, DT
McPherson, SA
Levasseur, DN
Sorscher, EJ
机构
[1] Univ Alabama Birmingham, Dept Med, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Pittman Gen Clin Res Ctr, Birmingham, AL 35294 USA
[3] Univ Alabama Birmingham, Dept Comp & Informat Sci, Birmingham, AL 35294 USA
[4] Univ Alabama Birmingham, Gregory Flemming James Cyst Fibrosis Ctr, Birmingham, AL 35294 USA
[5] Univ Alabama Birmingham, AIDS Res Ctr, Birmingham, AL 35294 USA
[6] Dana Farber Canc Inst, Dept Pediat Oncol, Boston, MA 02115 USA
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2006年 / 11卷
关键词
intron; function; micro-RNA; regulation; transcription; gene signalling;
D O I
10.2741/1941
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
MicroRNAs (miRNAs) have been suggested as suppressors of numerous target genes in human cells. In this report, we present gene chip array data indicating that in the absence of miRNA sequences, complete human introns are similarly capable of coordinating expression of large numbers of gene products at spatially diverse sites within the genome. The expression of selected intronic sequences (6a, 14b and 23) derived from the cystic fibrosis transmembrane conductance regulator (CFTR) gene caused extensive and specific transcriptional changes in epithelial cells (HeLa) that do not normally express this gene product. Each intron initiated a distinctive pattern of gene transcription. Affected genes such as FOXF1, sucrase-isomaltase, collagen, interferon, complement and thrombospondin 1 have previously been linked to CFTR function or are known to contribute to the related processes of epithelial differentiation and repair. A possible regulatory function of this nature has not been demonstrated previously for non-coding sequences within eukaryotic DNA. The results are consistent with the observation that splicesomal introns are found only in eukaryotic organisms and that the number of introns increases with phylogenetic complexity.
引用
收藏
页码:1998 / 2006
页数:9
相关论文
共 36 条
  • [1] NOVEL MECHANISM FOR RNA MATURATION - LEADER SEQUENCES OF SIMIAN VIRUS-40 MESSENGER-RNA ARE NOT TRANSCRIBED ADJACENT TO CODING SEQUENCES - [SPLICED RNA MESSENGER-RNA DNA HYBRIDS RNA PROCESSING CAP STRUCTURES POLY(A)]
    ALONI, Y
    DHAR, R
    LAUB, O
    HOROWITZ, M
    KHOURY, G
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (09) : 3686 - 3690
  • [2] A handful of intron-containing genes produces the lion's share of yeast mRNA
    Ares, M
    Grate, L
    Pauling, MH
    [J]. RNA, 1999, 5 (09) : 1138 - 1139
  • [3] Introns resolve the conflict between base order-dependent stem-loop potential and the encoding of RNA or protein: further evidence from overlapping genes
    Barrette, IH
    McKenna, S
    Taylor, DR
    Forsdyke, DR
    [J]. GENE, 2001, 270 (1-2) : 181 - 189
  • [4] Microarray profiling of microRNAs reveals frequent coexpression with neighboring miRNAs and host genes
    Baskerville, S
    Bartel, DP
    [J]. RNA, 2005, 11 (03) : 241 - 247
  • [5] Eukaryotic non-coding DNA is functional: evidence from the differential scaling of cryptomonad genomes
    Beaton, MJ
    Cavalier-Smith, T
    [J]. PROCEEDINGS OF THE ROYAL SOCIETY B-BIOLOGICAL SCIENCES, 1999, 266 (1433) : 2053 - 2059
  • [6] SPLICED SEGMENTS AT 5' TERMINUS OF ADENOVIRUS 2 LATE MESSENGER-RNA
    BERGET, SM
    MOORE, C
    SHARP, PA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1977, 74 (08) : 3171 - 3175
  • [7] CELMA ML, 1977, NUCLEIC ACIDS RES, V4, P2549
  • [8] AMAZING SEQUENCE ARRANGEMENT AT 5' ENDS OF ADENOVIRUS-2 MESSENGER-RNA
    CHOW, LT
    GELINAS, RE
    BROKER, TR
    ROBERTS, RJ
    [J]. CELL, 1977, 12 (01) : 1 - 8
  • [9] Adenosine and its nucleotides activate wild-type and R117H CFTR through an A2B receptor-coupled pathway
    Clancy, JP
    Ruiz, FE
    Sorscher, EJ
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1999, 276 (02): : C361 - C369
  • [10] Thrombospondin-1 is a major activator of TGF-β1 in vivo
    Crawford, SE
    Stellmach, V
    Murphy-Ullrich, JE
    Ribeiro, SMF
    Lawler, J
    Hynes, RO
    Boivin, GP
    Bouck, N
    [J]. CELL, 1998, 93 (07) : 1159 - 1170