Arabinogalactan protein profiles and distribution patterns during microspore embryogenesis and pollen development in Brassica napus

• Type: Article in International Scientific Journal
• Date: 2013

Authors

Ahmed Abdalla El Tantawy (Author) Other; Maria Teresa Solis (Author) Other; Mario L Da Costa (Author) Other; Silvia Coimbra (Author) FCUP; Maria Carmen Risueno (Author) Other; Pilar S Testillano (Author) Other

Journal

Title: Plant Reproduction

Vol. 26

Pages: 231-243

ISSN: 2194-7953

Publisher: Springer Nature

Indexing

ISI Web of Knowledge - 47 Citations

Scopus - 47 Citations

Scientific classification

FOS: Natural sciences > Biological sciences

Other information

Authenticus ID: P-006-7TG

DOI: 10.1007/s00497-013-0217-8

Abstract (EN): Arabinogalactan proteins (AGPs), present in cell walls, plasma membranes and extracellular secretions, are massively glycosylated hydroxyproline-rich proteins that play a key role in several plant developmental processes. After stress treatment, microspores cultured in vitro can reprogramme and change their gametophytic developmental pathways towards embryogenesis, thereby producing embryos which can further give rise to haploid and double haploid plants, important biotechnological tools in plant breeding. Microspore embryogenesis constitutes a convenient system for studying the mechanisms underlying cell reprogramming and embryo formation. In this work, the dynamics of both AGP presence and distribution were studied during pollen development and microspore embryogenesis in Brassica napus, by employing a multidisciplinary approach using monoclonal antibodies for AGPs (LM2, LM6, JIM13, JIM14, MAC207) and analysing the expression pattern of the BnAGP Sta 39-4 gene. Results showed the developmental regulation and defined localization of the studied AGP epitopes during the two microspore developmental pathways, revealing different distribution patterns for AGPs with different antigenic reactivity. AGPs recognized by JIM13, JIM14 and MAC207 antibodies were related to pollen maturation, whereas AGPs labelled by LM2 and LM6 were associated with embryo development. Interestingly, the AGPs labelled by JIM13 and JIM14 were induced with the change of microspore fate. Increases in the expression of the Sta 39-4 gene, JIM13 and JIM14 epitopes found specifically in 2-4 cell stage embryo cell walls, suggested that AGPs are early molecular markers of microspore embryogenesis. Later, LM2 and LM6 antigens increased progressively with embryo development and localized on cell walls and cytoplasmic spots, suggesting an active production and secretion of AGPs during in vitro embryo formation. These results give new insights into the involvement of AGPs as potential regulating/signalling molecules in microspore reprogramming and embryogenesis.

Language: English

Type (Professor's evaluation): Scientific

No. of pages: 13