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Origin, timing, and gene expression profile of adventitious rooting in Arabidopsis hypocotyls and stems

Welander, Margareta (författare)
Swedish University of Agricultural Sciences,Sveriges lantbruksuniversitet,Institutionen för växtförädling,Department of Plant Breeding
Smolka, Anders (författare)
Swedish University of Agricultural Sciences,Sveriges lantbruksuniversitet,VÄXTFÖRÄDLING, Box 101,VÄXTFÖRÄDLING, Box 101
Ahlman, Annelie (författare)
Swedish University of Agricultural Sciences,Sveriges lantbruksuniversitet,Institutionen för växtförädling,Department of Plant Breeding
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Fan, Jing (författare)
Swedish University of Agricultural Sciences,Sveriges lantbruksuniversitet,VÄXTFÖRÄDLING, Box 101,VÄXTFÖRÄDLING, Box 101
Zhu, Li-Hua (författare)
Swedish University of Agricultural Sciences,Sveriges lantbruksuniversitet,Institutionen för växtförädling,Department of Plant Breeding
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 (creator_code:org_t)
 
2014-02-01
2014
Engelska.
Ingår i: American Journal of Botany. - : Wiley. - 0002-9122 .- 1537-2197. ; 101, s. 255-266
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Premise of the study: Adventitious root (AR) formation is indispensable for vegetative propagation, but diffi cult to achieve in many crops. Understanding its molecular mechanisms is thus important for such species. Here we aimed at developing a rooting protocol for direct AR formation in stems, locating cellular AR origins in stems and exploring molecular differences underlying adventitious rooting in hypocotyls and stems. Methods: In-vitro-grown hypocotyls or stems of wild-type and transgenic ecotype Columbia (Col-0) of Arabidopsis thalianawere rooted on rooting media. Anatomy of AR formation, qRT-PCR of some rooting-related genes and in situ GUS expression were carried out during rooting from hypocotyls and stems. Key results: We developed a rooting protocol for AR formation in stems and traced back root origins in stems by anatomicaland in situ expression studies. Unlike rooting in hypocotyls, rooting in stems was slower, and AR origins were mainly from lateral parenchyma of vascular bundles and neighboring starch sheath cells as well as, to a lesser extent, from phloem cap and xylem parenchyma. Transcript levels of GH3-3 , LBD16 , LBD29 , and LRP1 in hypocotyls and stems were similar, but transcript accumulation was delayed in stems. In situ expression signals of DR5::GUS , LBD16::GUS , LBD29::GUS , and rolB::GUS reporters in stems mainly occurred at the root initiation sites, suggesting their involvement in AR formation. Conclusions: We have developed an effi cient rooting protocol using half-strength Lepoivre medium for studying AR formation instems, traced back the cellular AR origins in stems, and correlated expression of rooting-related genes with root initiation sites.

Ämnesord

NATURVETENSKAP  -- Biologi -- Utvecklingsbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Developmental Biology (hsv//eng)

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