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Differential gene expression in proteoid root clusters of white lupin ( Lupinus albus )
Author(s) -
Peñaloza Enrique,
Gutierrez Ana,
Martínez José,
Muñoz Gastón,
Bravo León A.,
Corcuera Luis J.
Publication year - 2002
Publication title -
physiologia plantarum
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.351
H-Index - 146
eISSN - 1399-3054
pISSN - 0031-9317
DOI - 10.1034/j.1399-3054.2002.1160104.x
Subject(s) - biology , lupinus , differential display , gene , complementary dna , microbiology and biotechnology , gene expression , coding region , population , biochemistry , genetics , botany , demography , sociology
Proteoid root clusters are induced by P deficiency in white lupin. In their mature stage, these roots excrete organic acids (mainly citrate), thus allowing this species to acquire P from sparingly soluble sources. To screen for P‐regulated genes expressed during the period of citrate efflux, an experimental model based on proteoid root clusters contrasting in citrate efflux was developed. The feasibility of this model in identifying differential gene expression was assessed over a population of mRNAs from P‐starved and P‐starved rescued proteoid root clusters, sampled 24 and 72 h after P addition to 24 days P‐starved white lupin. Approximately 1500 bands of cDNA were displayed by differential display of 21‐primer pair's combination; 52 differentially expressed bands, either up‐ or down‐regulated after P addition, were observed. Sequence analysis of 17 of them revealed that they represent distinct cDNAs. A subsample of seven cDNAs was analysed by northern‐blot, showing that six were truly differential products. Transcripts coding for enzymes involved in carbon flux (glyceraldehyde 3‐phosphate dehydrogenase), glycolytic bypass (phosphoenolpyruvate carboxylase), P i recycling (sulpholipid synthase), and two unknown cDNAs were shown to be down‐regulated by P supply. Besides, an up‐regulated transcript coding for a putative auxin‐induced protein was identified, whereas P addition did not significantly affect expression of a transcript for cyclophilins. These results show the feasibility of using P‐starved and P‐starved rescued proteoid root clusters as an experimental model to detect and examine the molecular changes occurring in root clusters during the period of citrate efflux in white lupin.