Nishizawa Y, Kishimoto N, Saito A, Hibi T
National Institute of Agrobiological Resources, Ibaraki, Japan.
Mol Gen Genet. 1993 Oct;241(1-2):1-10. doi: 10.1007/BF00280194.
Rice chitinases are encoded by a small multigene family. To clarify the overall organization of rice chitinase genes, we have isolated and characterized the genes Cht-1, Cht-2 and Cht-3. Although all the three genes encode class I chitinase, the nucleotide sequences of the coding regions of Cht-1 and Cht-3 are very similar (90%), while that of Cht-2 is clearly more divergent (78%). Only Cht-2 has a 130 bp intron and encodes a C-terminal peptide sequence similar to that known to function as a vacuolar targeting signal. In 5' flanking regions of Cht-1 and Cht-3, but not of Cht-2, conserved sequences (GGCCGGCYGCCCYAG) were found. Related sequences were found also in the 5' flanking regions of another chitinase gene and a beta-glucanase gene which has also been reported to be stress-induced in rice. RNA blot hybridization analysis demonstrated that the stress-induced expression patterns of the Cht-1 and Cht-3 genes are similar, but quite different from that of Cht-2. However, all three genes are active in unstressed roots. By restriction fragment length polymorphism (RFLP) linkage analysis, Cht-1 and Cht-3 were mapped onto chromosome 6 and shown to be closely linked (0.8 cM). Cht-2 was mapped onto chromosome 5. All these features suggest that the expression patterns of rice class I chitinase genes may be correlated with their levels of sequence divergence and their chromosomal location.
水稻几丁质酶由一个小的多基因家族编码。为了阐明水稻几丁质酶基因的整体结构,我们分离并鉴定了Cht-1、Cht-2和Cht-3基因。尽管这三个基因都编码I类几丁质酶,但Cht-1和Cht-3编码区的核苷酸序列非常相似(90%),而Cht-2的序列差异明显更大(78%)。只有Cht-2有一个130 bp的内含子,并编码一个C末端肽序列,类似于已知的作为液泡靶向信号起作用的序列。在Cht-1和Cht-3的5'侧翼区域,但不是Cht-2的,发现了保守序列(GGCCGGCYGCCCYAG)。在另一个几丁质酶基因和一个据报道在水稻中也受胁迫诱导的β-葡聚糖酶基因的5'侧翼区域也发现了相关序列。RNA印迹杂交分析表明,Cht-1和Cht-3基因的胁迫诱导表达模式相似,但与Cht-2的模式有很大不同。然而,所有三个基因在未受胁迫的根中都有活性。通过限制性片段长度多态性(RFLP)连锁分析,Cht-1和Cht-3被定位到第6号染色体上,并显示紧密连锁(0.8 cM)。Cht-2被定位到第5号染色体上。所有这些特征表明,水稻I类几丁质酶基因的表达模式可能与其序列差异水平和染色体定位相关。