Bagnoli F, Giannino D, Caparrini S, Camussi A, Mariotti D, Racchi M L
Sezione di Genetica, Dipartimento di Biotecnologie Agrarie, Università degli Studi di Firenze, Piazzale delle Cascine 24, 50144 Florence, Italy.
Mol Genet Genomics. 2002 May;267(3):321-8. doi: 10.1007/s00438-002-0664-7. Epub 2002 Apr 17.
Two cDNA clones encoding mitochondrial manganese superoxide dismutases (MnSODs) from peach ( Prunus persica [L.] Batsch) were identified, which show homologies to several plant MnSODs. The amino acid sequence predicted from one full-length clone ( MnSOD1) showed the highest homology to an MnSOD from Nicotiana plumbaginifolia (94%) and included a 24-amino acid transit peptide typical of those used to target proteins to the mitochondria. A second, partial clone ( MnSOD2) showed divergence from MnSOD1 in the 3' untranslated region. It could therefore derive from a second gene or from an allele of MnSOD1. Southern hybridisation analysis suggests the existence of two MnSOD genes in peach. SOD isoenzyme profiles, MnSOD1 expression and protein levels were studied in aerial vegetative tissues derived from plants of different ages and in adult plants during the seasonal cycle. Zymograms revealed at least two isoforms of MnSODs in pre-shooting vegetative buds and in developing fruits. Levels of MnSODs were lower in leaves derived from apical shoots of adult plants than in leaves derived from seedlings, basal shoots or in vitro propagated juvenile plants, which are considered as juvenile-like structures. The MnSOD1 transcript and protein followed the same pattern. The results suggest that the steady-state levels of MnSOD1 mRNA in leaves vary with both the ontogenetic stage and the growth rate of the tissues examined.
鉴定出了两个编码桃(Prunus persica [L.] Batsch)线粒体锰超氧化物歧化酶(MnSOD)的cDNA克隆,它们与几种植物MnSOD具有同源性。从一个全长克隆(MnSOD1)预测的氨基酸序列与来自烟草(Nicotiana plumbaginifolia)的MnSOD具有最高同源性(94%),并包含一个24个氨基酸的转运肽,这是用于将蛋白质靶向线粒体的典型转运肽。第二个部分克隆(MnSOD2)在3'非翻译区与MnSOD1存在差异。因此,它可能来自第二个基因或MnSOD1的一个等位基因。Southern杂交分析表明桃中存在两个MnSOD基因。对来自不同年龄植株的地上营养组织以及成年植株在季节周期中的SOD同工酶谱、MnSOD1表达和蛋白质水平进行了研究。酶谱显示在芽前营养芽和发育中的果实中至少有两种MnSOD同工型。成年植株顶梢叶片中的MnSOD水平低于幼苗、基部梢或离体繁殖的幼年植株(被视为类幼年结构)叶片中的MnSOD水平。MnSOD1转录本和蛋白质呈现相同模式。结果表明,叶片中MnSOD1 mRNA的稳态水平随所检测组织的个体发育阶段和生长速率而变化。