INVESTIGADORES
CHAN Raquel Lia
congresos y reuniones científicas
Título:
Functional characterization of MTHB1, a Medicago truncatula HD-Zip transcription factor
Autor/es:
CAPELLA M; ARIEL FD; DEZAR CA; CHAN RL
Lugar:
San Miguel de Tucumán
Reunión:
Congreso; XLV Reunión Anual de la Sociedad Argentina de Investigación en Bioquímica y Biología Molecular; 2009
Institución organizadora:
SAIB
Resumen:
Functional characterization of the Medicago HD-Zip Transcription Factor MTHB1 in the aerial organs.Capella M, Ariel FD, Dezar CA, and Chan RLInstituto de Agrobiotecnología del Litoral- UNL-CONICET- CP 3000 Santa Ferchan@fbcb.unl.edu.ar ABSTRACT MTHB1 is a Medicago truncatula  gene encoding a HD-Zip I transcription factor (TF); up-regulated by salt stress and hormones in roots. It was previously reported that this TF acts as a negative regulator of MTLBD1, a LOB-Like TF involved in lateral roots promoting; however, no information is available about the function of this gene in the aerial organs of the plant.A DNA segment corresponding to the promoter region of MTHB1 was isolated by PCR using genomic DNA and specific oligonucleotides and cloned into the pKGWFS7 vector directing the expression of the GUS reporter gene. Transgenic Medicago roots were obtained with this construct and were subjected to salt stress and ABA. These experiments indicated that both treatments enhanced MTHB1 expression, in agreement with its potential function. Using the same construct, Arabidopsis plants were transformed and the expression pattern of GUS analyzed by histochemistry. As expected, this gene turned out to be expressed in roots, but also in certain regions of the SAM. MTHB1 expression pattern is consistent with those of the homologous in Arabidopsis, ATHB7 and 12.TILLING mutant homozygous Medicago plants, unable to express a functional MTHB1, exhibited a particular aerial phenotype with multiple branches in comparison with the WT genotype.The aerial expression pattern, together with the mthb1 plants phenotype, suggests that MTHB1 is somehow involved in branch formation controlling SAM cells fate.