Caliskan Mahmut, Turet Müge, Cuming Andrew C
Centre for Plant Sciences, Leeds University, LS2 9JT, Leeds, UK.
Planta. 2004 May;219(1):132-40. doi: 10.1007/s00425-003-1199-9. Epub 2004 Jan 27.
In wheat ( Triticum aestivum L.), embryogenic callus formation comprises suppression of precocious germination by the zygotic embryo and the initiation of dedifferentiated cellular proliferation within it. Embryogenic calli are induced by treating immature embryos with 2,4-dichlorophenoxyacetic acid (2,4-D). Upon withdrawal from 2,4-D, somatic embryos develop from the periphery of the callus. Prior to visible callus formation, there is a striking induction of "germin-like" oxalate oxidase ("gl-OXO": EC 1.2.3.4) gene expression. Accumulation of gl-OXO mRNA is rapidly stimulated upon auxin treatment, with a consequent development of apoplastic enzyme activity producing H(2)O(2) within the cell wall. Within the dedifferentiated calli, gl-OXO enzyme activity becomes widespread over the surface of embryogenic calli. Differentiation of somatic embryos is initiated in regions of densely cytoplasmic, meristematic cells that are marked by highly localised expression of gl-OXO activity within these embryogenic cell masses. We suggest that this localised generation of H(2)O(2) by gl-OXO promotes peroxidative cross-linking of cell wall components, thereby preventing cellular expansion and maintaining these cell masses in an embryogenically competent condition.
在小麦(普通小麦)中,胚性愈伤组织的形成包括合子胚对早熟萌发的抑制以及胚内去分化细胞增殖的启动。用2,4-二氯苯氧乙酸(2,4-D)处理未成熟胚可诱导形成胚性愈伤组织。从2,4-D中撤出后,体细胞胚从愈伤组织的周边发育而来。在可见愈伤组织形成之前,会显著诱导“类萌发”草酸氧化酶(“gl-OXO”:EC 1.2.3.4)基因的表达。生长素处理后,gl-OXO mRNA迅速积累,随后在细胞壁内产生质外体酶活性,生成H₂O₂。在去分化的愈伤组织中,gl-OXO酶活性在胚性愈伤组织表面广泛分布。体细胞胚的分化始于细胞质浓密的分生细胞区域,这些区域以这些胚性细胞团内gl-OXO活性的高度局部化表达为特征。我们认为,gl-OXO局部产生的H₂O₂促进了细胞壁成分的过氧化交联,从而阻止细胞扩张,并使这些细胞团保持在胚性感受态状态。