Filichkin Sergei A, Leonard Jeffrey M, Monteros Alvaro, Liu Po-Pu, Nonogaki Hiroyuki
Department of Horticulture, Oregon State University, Corvallis, Oregon 97331-7304, USA.
Plant Physiol. 2004 Mar;134(3):1080-7. doi: 10.1104/pp.103.035998. Epub 2004 Feb 19.
Endo-beta-mannanase (EC 3.2.1.78) is involved in cell wall disassembly and the weakening of plant tissues by degrading mannan polymers in the cell walls. Endo-beta-mannanase genes are expressed in tomato (Lycopersicon esculentum) seeds (LeMAN1 and LeMAN2) and fruits (LeMAN3 and LeMAN4). A novel endo-beta-mannanase gene (termed LeMAN5) was found in the tomato genome by genome-walking PCR and bacterial artificial chromosome library screening. The 5'-upstream region of this endo-beta-mannanase gene contained four copies of the pollen-specific cis-acting elements POLLEN1LELAT52 (AGAAA). A GUS-reporter gene driven with the putative LeMAN5 promoter (-543 to +38) was activated in anthers and pollen of transgenic Arabidopsis, with the highest beta-glucuronidase activity detected in pollen. beta-Glucuronidase expression was detected in mature pollen retained in sporangia, discharged pollen, and elongating pollen tubes in transgenic Arabidopsis. Consistently, expression of LeMAN5 mRNA and endo-beta-mannnanase activity was detected in tomato anthers and pollen. In anthers, the highest mRNA expression and endo-beta-mannanase activity were detected during late stages of anther development, when pollen maturation occurred. Endo-beta-mannanase activity was present in discharged pollen, which was easily eluted in a buffer, indicating that the enzyme proteins are probably secreted from, and deposited on, the surface of pollen. These data suggest that the LeMAN5 endo-beta-mannanase is associated with anther and pollen development.
内切-β-甘露聚糖酶(EC 3.2.1.78)通过降解细胞壁中的甘露聚糖聚合物参与细胞壁的分解和植物组织的弱化。内切-β-甘露聚糖酶基因在番茄(Lycopersicon esculentum)种子(LeMAN1和LeMAN2)和果实(LeMAN3和LeMAN4)中表达。通过基因组步移PCR和细菌人工染色体文库筛选,在番茄基因组中发现了一个新的内切-β-甘露聚糖酶基因(命名为LeMAN5)。该内切-β-甘露聚糖酶基因的5'-上游区域包含四个花粉特异性顺式作用元件POLLEN1LELAT52(AGAAA)拷贝。由推定的LeMAN5启动子(-543至+38)驱动的GUS报告基因在转基因拟南芥的花药和花粉中被激活,在花粉中检测到最高的β-葡萄糖醛酸酶活性。在转基因拟南芥的孢子囊中保留的成熟花粉、排出的花粉和伸长的花粉管中检测到β-葡萄糖醛酸酶表达。同样,在番茄花药和花粉中检测到LeMAN5 mRNA的表达和内切-β-甘露聚糖酶活性。在花药中,在花药发育后期花粉成熟时检测到最高的mRNA表达和内切-β-甘露聚糖酶活性。排出的花粉中存在内切-β-甘露聚糖酶活性,其在缓冲液中很容易洗脱,表明酶蛋白可能从花粉表面分泌并沉积在花粉表面。这些数据表明LeMAN5内切-β-甘露聚糖酶与花药和花粉发育有关。