Liang X, Oono Y, Shen N F, Köhler C, Li K, Scolnik P A, Theologis A
Plant Gene Expression Center, Albany, CA 94710, USA.
Gene. 1995 Dec 29;167(1-2):17-24. doi: 10.1016/0378-1119(95)00694-x.
The nucleotide sequences of two highly homologous 1-aminocyclopropane-1-carboxylate (ACC) synthase (ACS; EC 4.4.1.14)-encoding genes, ACS1 and ACS3, of Arabidopsis thaliana (At) have been determined. The sequence analysis shows that ACS3 is a pseudogene representing a truncated version of ACS1. The missing region of ACS3 corresponding to the fourth exon of ACS1 has been shown by Southern analysis to be absent in the At genome. The chromosomal locations of the five members of the At ACS multigene family have been determined. The results show that each family member resides on a different chromosome. This observation suggests that the ACS3 pseudogene originated by a partial inter-chromosomal gene duplication. The ACS1 polypeptide contains all the conserved and characteristic domains found in the ACC synthase isoenzymes from various plant species, but is unable to express ACS activity in Escherichia coli and yeast. The predicted amino-acid sequence of ACS1 is missing the highly conserved tripeptide, Thr-Asn-Pro (TNP), between Ile204 and Ser205. Introduction of TNP into ACS1 restores the ACS activity, whereas its removal from the enzymatically active ACS2 results in a loss of activity. The results suggest that TNP is crucial for expression of ACS activity in E. coli.
已测定了拟南芥(At)两个高度同源的1-氨基环丙烷-1-羧酸(ACC)合酶(ACS;EC 4.4.1.14)编码基因ACS1和ACS3的核苷酸序列。序列分析表明,ACS3是一个假基因,代表ACS1的截短版本。通过Southern分析表明,ACS3对应于ACS1第四外显子的缺失区域在拟南芥基因组中不存在。已确定了拟南芥ACS多基因家族五个成员的染色体定位。结果表明,每个家族成员位于不同的染色体上。这一观察结果表明,ACS3假基因起源于部分染色体间基因重复。ACS1多肽包含在各种植物物种的ACC合酶同工酶中发现的所有保守和特征结构域,但在大肠杆菌和酵母中无法表达ACS活性。ACS1的预测氨基酸序列在Ile204和Ser205之间缺少高度保守的三肽Thr-Asn-Pro(TNP)。将TNP引入ACS1可恢复ACS活性,而从具有酶活性的ACS2中去除TNP则导致活性丧失。结果表明,TNP对于大肠杆菌中ACS活性的表达至关重要。