Trevino M B, OConnell M A
Graduate Program in Molecular Biology and Department of Agronomy and Horticulture, New Mexico State University, Las Cruces, 88003-8003, USA.
Plant Physiol. 1998 Apr;116(4):1461-8. doi: 10.1104/pp.116.4.1461.
Genomic clones of two nonspecific lipid-transfer protein genes from a drought-tolerant wild species of tomato (Lycopersicon pennellii Corr.) were isolated using as a probe a drought- and abscisic acid (ABA)-induced cDNA clone (pLE16) from cultivated tomato (Lycopersicon esculentum Mill.). Both genes (LpLtp1 and LpLtp2) were sequenced and their corresponding mRNAs were characterized; they are both interrupted by a single intron at identical positions and predict basic proteins of 114 amino acid residues. Genomic Southern data indicated that these genes are members of a small gene family in Lycopersicon spp. The 3'-untranslated regions from LpLtp1 and LpLtp2, as well as a polymerase chain reaction-amplified 3'-untranslated region from pLE16 (cross-hybridizing to a third gene in L. pennellii, namely LpLtp3), were used as gene-specific probes to describe expression in L. pennellii through northern-blot analyses. All LpLtp genes were exclusively expressed in the aerial tissues of the plant and all were drought and ABA inducible. Each gene had a different pattern of expression in fruit, and LpLtp1 and LpLtp2, unlike LpLtp3, were both primarily developmentally regulated in leaf tissue. Putative ABA-responsive elements were found in the proximal promoter regions of LpLtp1 and LpLtp2.
利用来自栽培番茄(Lycopersicon esculentum Mill.)的干旱和脱落酸(ABA)诱导的cDNA克隆(pLE16)作为探针,从耐旱野生番茄物种(Lycopersicon pennellii Corr.)中分离出两个非特异性脂质转移蛋白基因的基因组克隆。对这两个基因(LpLtp1和LpLtp2)进行了测序,并对其相应的mRNA进行了表征;它们都在相同位置被一个内含子打断,并预测有114个氨基酸残基的碱性蛋白。基因组Southern数据表明,这些基因是番茄属植物中一个小基因家族的成员。LpLtp1和LpLtp2的3'-非翻译区,以及来自pLE16的聚合酶链反应扩增的3'-非翻译区(与潘那利番茄中的第三个基因,即LpLtp3交叉杂交),被用作基因特异性探针,通过Northern杂交分析来描述潘那利番茄中的表达情况。所有LpLtp基因都只在植物的地上组织中表达,并且都受干旱和ABA诱导。每个基因在果实中的表达模式不同,与LpLtp3不同,LpLtp1和LpLtp2在叶组织中主要受发育调控。在LpLtp1和LpLtp2的近端启动子区域发现了假定的ABA反应元件。