4.8 Article

Molecular mechanisms and hormonal regulation underpinning morphological dormancy: a case study using Apium graveolens (Apiaceae)

Journal

PLANT JOURNAL
Volume 108, Issue 4, Pages 1020-1036

Publisher

WILEY
DOI: 10.1111/tpj.15489

Keywords

Apium graveolens (celery); auxin transport; ABA-gibberellin balance; dormancy evolution; embryo growth; endosperm breakdown; morphological dormancy; underdeveloped embryo

Categories

Funding

  1. TOMCAT beamline of the Swiss Light Source [20180809]
  2. Biotechnology and Biological Sciences Research Council (BBSRC) [BB/M011178/1, 1813810]
  3. BBSRC Research [BB/M02203X/1, BB/M00192X/1]
  4. European Regional Development Fund Project 'Plants as a tool for sustainable global development' [CZ.02.1.01/0.0/0.0/16_019/0000827]
  5. 'Centre for Experimental Plant Biology' [CZ.02.1.01/0.0/0.0/16_019/0000738]
  6. Czech Science Foundation [18-10349S]
  7. BBSRC [BB/M00192X/1, BB/M02203X/1, 1813810] Funding Source: UKRI

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Morphological dormancy (MD) in celery is considered ancestral in seed dormancy evolution, with embryo growth and endosperm breakdown occurring inside imbibed fruits. The critical size for embryo growth and endosperm breakdown associated with ABA degradation constitute a unique germination program.
Underdeveloped (small) embryos embedded in abundant endosperm tissue, and thus having morphological dormancy (MD) or morphophysiological dormancy (MPD), are considered to be the ancestral state in seed dormancy evolution. This trait is retained in the Apiaceae family, which provides excellent model systems for investigating the underpinning mechanisms. We investigated Apium graveolens (celery) MD by combined innovative imaging and embryo growth assays with the quantification of hormone metabolism, as well as the analysis of hormone and cell-wall related gene expression. The integrated experimental results demonstrated that embryo growth occurred inside imbibed celery fruits in association with endosperm degradation, and that a critical embryo size was required for radicle emergence. The regulation of these processes depends on gene expression leading to gibberellin and indole-3-acetic acid (IAA) production by the embryo and on crosstalk between the fruit compartments. ABA degradation associated with distinct spatiotemporal patterns in ABA sensitivity control embryo growth, endosperm breakdown and radicle emergence. This complex interaction between gibberellins, IAA and ABA metabolism, and changes in the tissue-specific sensitivities to these hormones is distinct from non-MD seeds. We conclude that the embryo growth to reach the critical size and the associated endosperm breakdown inside MD fruits constitute a unique germination programme.

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