Gibson S, Arondel V, Iba K, Somerville C
Department of Biochemistry and Cell Biology, Rice University, Houston, Texas 77251-1892.
Plant Physiol. 1994 Dec;106(4):1615-21. doi: 10.1104/pp.106.4.1615.
Previous genetic evidence suggested that the fad8 and fad7 genes of Arabidopsis thaliana encode chloroplast membrane-associated omega-3 desaturases. A putative fad8 cDNA was isolated by heterologous hybridization using a gene encoding an endoplasmic reticulum-localized omega-3 desaturase (fad3) as a probe. The cDNA encodes a protein of 435 amino acid residues with a molecular mass of 50,134 D. Constitutive expression of the cDNA in transgenic plants of a fad7 mutant resulted in genetic complementation of the mutation, indicating that the fad7 and fad8 gene products are functionally equivalent. Expression of the fad8 cDNA in transgenic plants often resulted in the co-suppression of both the endogenous fad7 and fad8 genes in spite of the fact that these two genes share only about 75% nucleotide identity. In contrast to all other known plant desaturases, including fad7, the steady-state level of fad8 mRNA is strongly increased in plants grown at low temperature. This suggests that the role of fad8 is to provide increased omega-3 desaturase activity in plants that are exposed to low growth temperature. The fad8-1 mutation created a premature stop codon 149 amino acids from the amino-terminal end of the fad8 open reading frame, suggesting that this mutation results in a complete loss of fad8 activity.
先前的遗传学证据表明,拟南芥的fad8和fad7基因编码与叶绿体膜相关的ω-3去饱和酶。使用编码内质网定位的ω-3去饱和酶(fad3)的基因作为探针,通过异源杂交分离出一个推定的fad8 cDNA。该cDNA编码一个由435个氨基酸残基组成的蛋白质,分子量为50,134 D。fad8 cDNA在fad7突变体的转基因植物中组成型表达导致该突变的遗传互补,表明fad7和fad8基因产物在功能上是等效的。尽管fad8 cDNA在转基因植物中的表达常常导致内源性fad7和fad8基因的共抑制,尽管这两个基因仅共享约75%的核苷酸同一性。与包括fad7在内的所有其他已知植物去饱和酶不同,fad8 mRNA的稳态水平在低温生长的植物中强烈增加。这表明fad8的作用是在暴露于低温生长的植物中提供增加的ω-3去饱和酶活性。fad8-1突变在fad8开放阅读框的氨基末端149个氨基酸处产生了一个提前终止密码子,表明该突变导致fad8活性完全丧失。