4.6 Article

Four abiotic stress-induced miRNA families differentially regulated in the embryogenic and non-embryogenic callus tissues of Larix leptolepis

期刊

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbrc.2010.06.056

关键词

Larix leptolepis; miRNA regulation; Embryogenesis; miR171; miR172

资金

  1. National Basic Research Program of China [2009CB119100]
  2. National Natural Science Foundation of China [30830086]
  3. National High Technology Research and Development Program of China [2006AA100109, 2007AA021403, 2007AA10Z182, 2008AA10Z126, 2007AA021501]
  4. National Bureau of Forestry 948 Program [2007-4-03]

向作者/读者索取更多资源

Somatic embryogenesis involves complex molecular signaling pathways. Deregulation of these signaling pathways can transform the emblyogenic callus to non-embryogenic callus. To investigate the miRNA regulation underlying this detrimental transformation in Japanese Larch (Larix leptolepis), we compared miRNA expression profiles between embryogenic and non-embryogenic callus at day 3 and day 14 after sub-culture. Four miRNA families dominated the 165 differentially expressed miRNAs between embryogenic and non-embryogenic callus. Of the four, miR171 was up-regulated, and miR159, miR169, and miR172 were down-regulated in the embryogenic callus. These four families are all abiotic stress-induced miRNAs, and all target transcription factors that regulate a group of genes important for cell differentiation and development, including scarecrow-like (SCL) transcription factor (miR171), apetala2 (miR172), MYB transcription factors (miR159), and NF-YA transcription factor (miR169). Three down-regulated miRNA families in the embryogenic callus are also regulated by ABA, which further shed light into the potential mechanisms underlying the transformation of the embryogenic competence in L. leptolepis. This study represents the first report on the miRNA regulation of the embryogenic and non-embryogenic callus in plant, and thus these four miRNA families provide important clues for further functional investigation. (C) 2010 Elsevier Inc. All rights reserved.

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