Shahar T, Hennig N, Gutfinger T, Hareven D, Lifschitz E
Department of Biology, Technion-Israel Institute of Technology, Haifa.
Plant Cell. 1992 Feb;4(2):135-47. doi: 10.1105/tpc.4.2.135.
A gene coding for a polypeptide abundant in tomato floral meristems was isolated and shown to represent a tomato 66.3-kD polyphenoloxidase. Analysis of cDNA clones and a corresponding intronless genomic clone indicated that the plastid-bound 587-residue-long polypeptide, designated P2, contains two conserved copper-binding domains, similar to those found in fungal and mammalian tyrosinases. P2 transcripts and polypeptides are accumulated in the arrested floral primordia of the anantha mutant inflorescences and are equally abundant in primordia of wild-type flowers; the gene continues to be expressed at high levels in developing floral organs. In young expanding leaves, P2 protein is concentrated in palisade cells and in epidermal trichomes. Expression patterns of P2 in plant meristems permit molecular distinction between floral and vegetative primordia, and, in a companion study, comparison with dUTPase suggests that the two genes mark two alternative complementary developmental programs in the floral and vegetative meristems of the tomato plants.
一个编码在番茄花分生组织中大量存在的多肽的基因被分离出来,结果表明它代表一种番茄66.3-kD多酚氧化酶。对cDNA克隆和相应的无内含子基因组克隆的分析表明,与质体结合的587个氨基酸长的多肽(命名为P2)含有两个保守的铜结合结构域,类似于在真菌和哺乳动物酪氨酸酶中发现的结构域。P2转录本和多肽在anantha突变体花序停滞的花原基中积累,并且在野生型花的原基中含量相同;该基因在发育中的花器官中继续高水平表达。在幼嫩的正在伸展的叶片中,P2蛋白集中在栅栏细胞和表皮毛中。P2在植物分生组织中的表达模式允许从分子水平区分花原基和营养原基,并且在一项配套研究中,与dUTPase的比较表明这两个基因在番茄植株的花分生组织和营养分生组织中标记了两个交替的互补发育程序。