首页> 美国卫生研究院文献>Plant Physiology >Rapid Alkalinization Factors in Poplar Cell Cultures. Peptide Isolation cDNA Cloning and Differential Expression in Leaves and Methyl Jasmonate-Treated Cells
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Rapid Alkalinization Factors in Poplar Cell Cultures. Peptide Isolation cDNA Cloning and Differential Expression in Leaves and Methyl Jasmonate-Treated Cells

机译:杨树细胞培养物中的快速碱化因子。叶片和茉莉酸甲酯处理过的细胞中的肽分离cDNA克隆和差异表达

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摘要

A family of peptides inducing rapid pH alkalinization in hybrid poplar (Populus trichocarpa × Populus deltoides) cell culture medium was isolated from hybrid poplar leaves. Five related approximately 5-kD peptides were purified by high-performance liquid chromatography and analyzed by matrix-assisted laser desorption ionization-mass spectrometry. The N-terminal sequence of one of the isolated peptides was very similar to a previously characterized peptide from tobacco (Nicotiana tabacum), rapid alkalinization factor (RALF), which causes a rapid increase in culture medium pH when added to tobacco cell cultures (G. Pearce, D.S. Moura, J. Stratmann, C.A. Ryan [2001] Proc Natl Acad Sci USA 98: 12843–12847). Two unique poplar RALF cDNAs (PtdRALF1 and PtdRALF2) were isolated from a poplar cDNA library and used to study RALF expression in poplar saplings and cultured poplar cells. Both genes were found to be expressed constitutively in poplar saplings and cultured cells. However, PtdRALF2 was expressed in leaves at very low levels, and its expression in suspension culture cells was transiently suppressed by methyl jasmonate (MeJa). Although the function of these novel peptides remains enigmatic, our experiments suggest their role may be developmental rather than stress related. Overall, our study confirms the presence of active RALF peptides in other plants, and provides new data on the complexity of the RALF gene family in poplar.
机译:从杂种杨树叶中分离出一个在杂种杨(Populus trichocarpa×Populus deltoides)细胞培养基中诱导pH快速碱化的肽家族。通过高效液相色谱法纯化了五个相关的约5 kD肽,并通过基质辅助激光解吸电离质谱法进行了分析。一种分离的肽的N端序列与烟草中先前鉴定的肽(Nicotiana tabacum)的快速碱化因子(RALF)非常相似,当添加到烟草细胞培养物中时,其会引起培养基pH的快速增加(G Pearce,DS Moura,J。Stratmann,CA Ryan [2001] Proc Natl Acad Sci USA 98:12843–12847)。从杨树cDNA文库中分离出两个独特的杨树RALF cDNA(PtdRALF1和PtdRALF2),并用于研究杨树树苗和培养的杨树细胞中的RALF表达。发现这两个基因在杨树幼树和培养的细胞中组成性表达。但是,PtdRALF2在叶片中的表达水平非常低,茉莉酸甲酯(MeJa)可以瞬时抑制其在悬浮培养细胞中的表达。尽管这些新型肽的功能仍然神秘,我们的实验表明它们的作用可能与发育有关,而不与压力有关。总体而言,我们的研究证实了其他植物中活性RALF肽的存在,并提供了有关杨树中RALF基因家族复杂性的新数据。

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