Yu L M, Lamb C J, Dixon R A
Plant Biology Division, Samuel Roberts Noble Foundation, Ardmore, OK 73402.
Plant J. 1993 Jun;3(6):805-16. doi: 10.1111/j.1365-313x.1993.00805.x.
The H-box (CCTACC(N)7CT(N)4A), which occurs three times within the -154 to -42 region of the bean chalcone synthase chs15 promoter, is important for developmental regulation of chs15, and induction of chs15 and coordinately regulated defense genes by elicitors and other stress stimuli. Two protein factors, KAP-1 and KAP-2, which recognize conserved features in the H-box motif, were purified from bean cell suspension cultures by a combination of ion exchange chromatography and DNA affinity chromatography. KAP-1 is a 97 kDa polypeptide, whereas KAP-2 comprises two polypeptides of 76 and 56 kDa. KAP-1 and KAP-2 also differ in the sensitivity of their DNA-bound forms to trypsin. Dephosphorylation of KAP-1 or KAP-2 affects the mobility of the protein/H-box binding complex in gel shift assays but does not inhibit DNA binding. Elicitation of bean cell suspensions with glutathione does not affect the total cellular activities of KAP-1 or KAP-2, but causes a rapid increase in the specific activities of both factors in the nuclear fraction, consistent with a role for these factors in the signal pathway for elicitor induction of chs15 and related defense genes.
H盒(CCTACC(N)7CT(N)4A)在菜豆查尔酮合酶chs15启动子的-154至-42区域内出现三次,对chs15的发育调控、chs15的诱导以及诱导子和其他应激刺激对防御基因的协同调控很重要。通过离子交换色谱和DNA亲和色谱相结合的方法,从菜豆细胞悬浮培养物中纯化出两种识别H盒基序保守特征的蛋白质因子KAP-1和KAP-2。KAP-1是一种97 kDa的多肽,而KAP-2由76 kDa和56 kDa的两种多肽组成。KAP-1和KAP-2与DNA结合的形式对胰蛋白酶的敏感性也不同。在凝胶迁移实验中,KAP-1或KAP-2的去磷酸化会影响蛋白质/H盒结合复合物的迁移率,但不会抑制DNA结合。用谷胱甘肽刺激菜豆细胞悬浮液不会影响KAP-1或KAP-2的总细胞活性,但会导致这两种因子在细胞核部分的比活性迅速增加,这与这些因子在诱导子诱导chs15和相关防御基因的信号通路中的作用一致。