Mølhøj M, Johansen B, Ulvskov P, Borkhardt B
Biotechnology Group, Danish Institute of Agricultural Sciences, Frederiksberg C.
Plant Mol Biol. 2001 Jan;45(1):93-105. doi: 10.1023/a:1006475908000.
A PCR fragment derived from a membrane-anchored endo-1,4-beta-glucanase cDNA was amplified using degenerated oligonucleotides and mRNA from oilseed rape (Brassica napus L.) siliques. Sequence analysis of the corresponding gene, Cel16, showed that the predicted Cel16 protein has high identity with the Arabidopsis KOR protein (94%). High-stringency genomic Southern analysis further revealed that Cel16 and KOR are most likely orthologous genes performing a similar function in both species. Northern blot and GUS analysis of transgenic Arabidopsis containing a fusion between a 2.0 kb Cel16 promoter fragment and the GUS reporter gene showed that Cel16 was expressed at a low level in the primary raceme, the young lateral stems, the elongation zone of the primary root and the older root base. By contrast, a high level of Cel16 mRNA accumulation was found in the young root and in the main stem carrying flowers and young siliques. Cel16 transcripts were localized to the apical meristem, cambium, primary xylem and cortex of oilseed rape stem tissue by in situ RT-PCR. A similar pattern of activity was found in the GUS analysis of transgenic Arabidopsis. Cel16 mRNA accumulation in the main stem was lower in the zone of most rapid cell elongation than in the subjacent, fully elongated internodes. Similarly, Cel16 transcripts accumulated to a higher level in leaves as they reached full size than during early leaf expansion. Analysis of the expression pattern in elongating, light-grown seedlings showed that Cel16 mRNA accumulated at a lower level in the elongating upper third than elsewhere in the hypocotyl. This is contrary to etiolated hypocotyls, where we found a higher expression level in the rapidly elongating upper part. This difference in expression most probably reflects a difference in cell wall assembly between light- and dark-grown seedlings.
利用简并寡核苷酸和来自油菜(Brassica napus L.)角果的mRNA,扩增得到一个源自膜锚定的内切-1,4-β-葡聚糖酶cDNA的PCR片段。对相应基因Cel16的序列分析表明,预测的Cel16蛋白与拟南芥KOR蛋白具有高度同源性(94%)。高严谨度的基因组Southern分析进一步表明,Cel16和KOR很可能是直系同源基因,在两个物种中发挥相似的功能。对含有2.0 kb Cel16启动子片段与GUS报告基因融合体的转基因拟南芥进行Northern杂交和GUS分析,结果显示Cel16在主花序、幼嫩侧茎、主根伸长区和较老的根基中低水平表达。相比之下,在幼根以及带有花和幼嫩角果的主茎中发现了高水平的Cel16 mRNA积累。通过原位RT-PCR发现,Cel16转录本定位于油菜茎组织的顶端分生组织、形成层、初生木质部和皮层。在转基因拟南芥的GUS分析中也发现了类似的活性模式。主茎中Cel16 mRNA的积累在细胞伸长最快的区域低于相邻的、完全伸长的节间。同样,叶片在达到完全大小后,Cel16转录本的积累水平高于叶片早期扩展阶段。对在光照下生长的伸长幼苗的表达模式分析表明,Cel16 mRNA在伸长的上三分之一区域的积累水平低于下胚轴的其他部位。这与黄化下胚轴相反,在黄化下胚轴中,我们发现在快速伸长的上部表达水平较高。这种表达差异很可能反映了光照和黑暗生长的幼苗在细胞壁组装方面的差异。