The Arabidopsis genome encodes for 10 Homeodomain-Leucine Zipper II (HD-Zip II) proteins. It has been previously shown that ATHB2, HAT1, HAT2 (HD-Zip II ? subfamily), HAT3 and ATHB4 (? subfamily) are induced by changes in the Red/Far Red ratio of the light environment. However, these genes are also tightly regulated during plant development with both distinct and overlapping patterns (Ciarbelli et al., Plant Mol. Biol. 2008, 68: 465-78). In order to understand the role of the light-regulated HD-Zip II genes in plant development, we have analyzed single and multiple mutants within ? and ? subfamilies. Here we present the phenotype of mutants in the HAT3 and ATHB4 genes. Young seedlings show a gradual loss of cotyledon and leaf expansion, up to completely radialized organs. The pattern of vascular development is also profoundly altered, in a manner that is tightly linked to lamina expansion. Fully radialized leaves lack procambial cells whereas trumpet shaped leaves show hyperproliferation of phloem with respect to xylem, a feature that is found in the vasculature of abaxialized leaves. In situ and GUS/GFP reporter analyses of the ? subfamily genes show that they are expressed in the adaxial side of cotyledons and leaves. Taken together, these data demonstrate that HAT3 and ATHB4 are required to specify adaxial identity in leaf morphogenesis. We are currently analyzing the molecular and genetic relationships between the ? HD-Zip II genes and members of the HD-Zip III family genes, such as PHB, PHV and REV, key determinants of adaxial leaf identity.
HD-Zip II transcription factor genes control adaxial-abaxial patterning in Arabidopsis leaf morphogenesis
Monica Carabelli;Luana Turchi;Massimiliano Sassi;Ida Ruberti
2011
Abstract
The Arabidopsis genome encodes for 10 Homeodomain-Leucine Zipper II (HD-Zip II) proteins. It has been previously shown that ATHB2, HAT1, HAT2 (HD-Zip II ? subfamily), HAT3 and ATHB4 (? subfamily) are induced by changes in the Red/Far Red ratio of the light environment. However, these genes are also tightly regulated during plant development with both distinct and overlapping patterns (Ciarbelli et al., Plant Mol. Biol. 2008, 68: 465-78). In order to understand the role of the light-regulated HD-Zip II genes in plant development, we have analyzed single and multiple mutants within ? and ? subfamilies. Here we present the phenotype of mutants in the HAT3 and ATHB4 genes. Young seedlings show a gradual loss of cotyledon and leaf expansion, up to completely radialized organs. The pattern of vascular development is also profoundly altered, in a manner that is tightly linked to lamina expansion. Fully radialized leaves lack procambial cells whereas trumpet shaped leaves show hyperproliferation of phloem with respect to xylem, a feature that is found in the vasculature of abaxialized leaves. In situ and GUS/GFP reporter analyses of the ? subfamily genes show that they are expressed in the adaxial side of cotyledons and leaves. Taken together, these data demonstrate that HAT3 and ATHB4 are required to specify adaxial identity in leaf morphogenesis. We are currently analyzing the molecular and genetic relationships between the ? HD-Zip II genes and members of the HD-Zip III family genes, such as PHB, PHV and REV, key determinants of adaxial leaf identity.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
