Bell-Lelong D A, Cusumano J C, Meyer K, Chapple C
Department of Biochemistry, Purdue University, West Lafayette, Indiana 47907, USA.
Plant Physiol. 1997 Mar;113(3):729-38. doi: 10.1104/pp.113.3.729.
Cinnamate-4-hydroxylase (C4H) is the first Cyt P450-dependent monooxygenase of the phenylpropanoid pathway. To study the expression of this gene in Arabidopsis thaliana, a C4H cDNA clone from the Arabidopsis expressed sequence tag database was identified and used to isolate its corresponding genomic clone. The entire C4H coding sequence plus 2.9 kb of its promoter were isolated on a 5.4-kb HindIII fragment of this cosmid. Inspection of the promoter sequence revealed the presence of a number of putative regulatory motifs previously identified in the promoters of other phenylpropanoid pathway genes. The expression of C4H was analyzed by RNA blot hybridization analysis and in transgenic Arabidopsis carrying a C4H-beta-glucuronidase transcriptional fusion. C4H message accumulation was light-dependent, but was detectable even in dark-grown seedlings. Consistent with these data, C4H mRNA was accumulated to light-grown levels in etiolated det1-1 mutant seedlings. C4H is widely expressed in various Arabidopsis tissues, particularly in roots and cells undergoing lignification. The C4H-driven beta-glucuronidase expression accurately reflected the tissue-specificity and wound-inducibility of the C4H promoter indicated by RNA blot hybridization analysis. A modest increase in C4H expression was observed in the tt8 mutant of Arabidopsis.
肉桂酸 - 4 - 羟化酶(C4H)是苯丙烷类途径中第一个依赖细胞色素P450的单加氧酶。为了研究该基因在拟南芥中的表达,从拟南芥表达序列标签数据库中鉴定出一个C4H cDNA克隆,并用于分离其相应的基因组克隆。在该粘粒的一个5.4 kb HindIII片段上分离出整个C4H编码序列及其2.9 kb的启动子。对启动子序列的检查揭示了在其他苯丙烷类途径基因的启动子中先前鉴定出的许多推定调控基序的存在。通过RNA印迹杂交分析以及在携带C4H - β - 葡萄糖醛酸酶转录融合体的转基因拟南芥中分析了C4H的表达。C4H信息积累是光依赖性的,但即使在黑暗生长的幼苗中也可检测到。与这些数据一致,C4H mRNA在黄化的det1 - 1突变体幼苗中积累到光生长水平。C4H在拟南芥的各种组织中广泛表达,特别是在根和正在进行木质化的细胞中。由RNA印迹杂交分析表明,C4H驱动的β - 葡萄糖醛酸酶表达准确反映了C4H启动子的组织特异性和伤口诱导性。在拟南芥的tt8突变体中观察到C4H表达有适度增加。