Details

Autor(en) / Beteiligte

• Clark, Anna M.
• Jacobsen, Karin R.
• Bostwick, Dwight E.
• Dannenhoffer, Joanne M.
• Skaggs, Megan I.
• Thompson, Gary A.

Titel

Molecular characterization of a phloem‐specific gene encoding the filament protein, Phloem Protein 1 (PP1), from Cucurbita maxima

Ist Teil von

• The Plant journal : for cell and molecular biology, 1997-07, Vol.12 (1), p.49-61

Ort / Verlag

Osney Mead, Oxford OX2 0EL, UK: Blackwell Science Ltd

Erscheinungsjahr

1997

Quelle

Wiley Online Library Journals Frontfile Complete

Beschreibungen/Notizen

• Summary Sieve elements in the phloem of most angiosperms contain proteinaceous filaments and aggregates called P‐protein. In the genus Cucurbita, these filaments are composed of two major proteins: PP1, the phloem filament protein, and PP2, the phloem lectin. The gene encoding the phloem filament protein in pumpkin (Cucurbita maxima Duch.) has been isolated and characterized. Nucleotide sequence analysis of the reconstructed gene gPP1 revealed a continuous 2430 bp protein coding sequence, with no introns, encoding an 809 amino acid polypeptide. The deduced polypeptide had characteristics of PP1 and contained a 15 amino acid sequence determined by N‐terminal peptide sequence analysis of PP1. The sequence of PP1 was highly repetitive with four 200 amino acid sequence domains containing structural motifs in common with cysteine proteinase inhibitors. Expression of the PP1 gene was detected in roots, hypocotyls, cotyledons, stems, and leaves of pumpkin plants. PP1 and its mRNA accumulated in pumpkin hypocotyls during the period of rapid hypocotyl elongation after which mRNA levels declined, while protein levels remained elevated. PP1 was immunolocalized in slime plugs and P‐protein bodies in sieve elements of the phloem. Occasionally, PP1 was detected in companion cells. PP1 mRNA was localized by in situ hybridization in companion cells at early stages of vascular differentiation. The developmental accumulation and localization of PP1 and its mRNA paralleled the phloem lectin, further suggesting an interaction between these phloem‐specific proteins.