Department of Forestry and Environmental Resources, North Carolina State University, Raleigh, NC 27695, USA.
Plant Cell Physiol. 2010 Jan;51(1):144-63. doi: 10.1093/pcp/pcp175. Epub 2009 Dec 8.
As a step toward a comprehensive description of lignin biosynthesis in Populus trichocarpa, we identified from the genome sequence 95 phenylpropanoid gene models in 10 protein families encoding enzymes for monolignol biosynthesis. Transcript abundance was determined for all 95 genes in xylem, leaf, shoot and phloem using quantitative real-time PCR (qRT-PCR). We identified 23 genes that most probably encode monolignol biosynthesis enzymes during wood formation. Transcripts for 18 of the 23 are abundant and specific to differentiating xylem. We found evidence suggesting functional redundancy at the transcript level for phenylalanine ammonia-lyase (PAL), cinnamate 4-hydroxylase (C4H), 4-coumarate:CoA ligase (4CL), p-hydroxycinnamoyl-CoA:quinate shikimate p-hydroxycinnamoyltransferase (HCT), caffeoyl-CoA O-methyltransferase (CCoAOMT) and coniferyl aldehyde 5-hydroxylase (CAld5H). We carried out an enumeration-based motif identification and discriminant analysis on the promoters of all 95 genes. Five core motifs correctly discriminate the 18 xylem-specific genes from the 77 non-xylem genes. These motifs are similar to promoter elements known to regulate phenylpropanoid gene expression. This work suggests that genes in monolignol biosynthesis are regulated by multiple motifs, often related in sequence.
为了全面描述杨树木质素的生物合成,我们从基因组序列中鉴定了 10 个蛋白家族的 95 个苯丙烷类基因模型,这些基因编码用于单酚生物合成的酶。使用定量实时 PCR (qRT-PCR) 测定了所有 95 个基因在木质部、叶、茎和韧皮部中的转录丰度。我们鉴定了 23 个在木材形成过程中最有可能编码单酚生物合成酶的基因。在 23 个基因中,有 18 个基因的转录物丰富且特异于分化的木质部。我们发现了在苯丙氨酸解氨酶 (PAL)、肉桂酸 4-羟化酶 (C4H)、4-香豆酸:CoA 连接酶 (4CL)、对羟基肉桂酰-CoA:奎宁酸莽草酸对羟基肉桂酰转移酶 (HCT)、咖啡酰-CoA-O-甲基转移酶 (CCoAOMT) 和松柏醛 5-羟化酶 (CAld5H) 的转录水平上存在功能冗余的证据。我们对所有 95 个基因的启动子进行了基于枚举的基序识别和判别分析。5 个核心基序可以正确地区分 18 个木质部特异基因和 77 个非木质部基因。这些基序类似于已知调节苯丙烷类基因表达的启动子元件。这项工作表明,木质素生物合成基因受到多个基序的调控,这些基序通常在序列上相关。