拟南芥
生物化学
酰基转移酶
酰基转移酶
生物
互补
突变体
基因
异源表达
酶
异源的
拟南芥
生物合成
酰基辅酶A
亚麻荠
转基因
二酰甘油激酶
内含子
转化(遗传学)
基因表达
转基因作物
花粉
内生
代谢工程
代谢途径
遗传学
细胞生物学
调节顺序
基因表达调控
双分子荧光互补
作者
Sean McGuire,Jay Shockey,Mark Richards,Andrei Smertenko,Philip D. Bates
出处
期刊:Plant Physiology
[Oxford University Press]
日期:2025-10-29
卷期号:199 (3)
被引量:2
标识
DOI:10.1093/plphys/kiaf552
摘要
Acyl-CoA:diacylglycerol acyltransferase 1 (DGAT1) and phospholipid:diacylglycerol acyltransferase 1 (PDAT1) share responsibility for triacylglycerol (TAG) biosynthesis, and their selectivities control TAG fatty acid (FA) compositions. For rational metabolic engineering of seed oils, replacing endogenous TAG biosynthesis with exogenous enzymes containing different substrate FA selectivities is desirable; however, the dgat1-1/pdat1-2 double mutant is pollen lethal. Here, we evaluated the ability of 3 DGAT1s, from phylogenetically diverse plants with distinct TAG assembly processes, to completely replace endogenous TAG biosynthesis in Arabidopsis (Arabidopsis thaliana). We transformed dgat1-1 mutant plants with expression constructs for DGAT1s from Camelina sativa, Physaria fendleri, and castor (Ricinus communis). Transgene expression was properly "contextualized" by using a previously determined minimum necessary expression unit containing the promoter/5' UTR and first intron of native AtDGAT1; both of these DNA elements are essential for pollen expression. Next, we crossed homozygous lines with a DGAT1/DGAT1/PDAT1/pdat1-2 parent. C. sativa and P. fendleri DGAT1s restored the FA compositions and transcriptional differences of dgat1-1 to near wild-type and rescued the dgat1-1/pdat1-2 pollen lethality. R. communis DGAT1 was active in dgat1-1 seeds but produced unique oil profiles and alterations in the expression of lipid metabolic genes; it also failed to rescue dgat1-1/pdat1-2 lethality. This study confirms that the promoter and first intron of AtDGAT1 can modulate the expression of foreign DGAT1 genes to fit the correct spatiotemporal profile necessary for completely replacing endogenous TAG biosynthesis. Furthermore, it demonstrates an additional layer of unexpected enzyme incompatibility between oilseed lineages, which may complicate bioengineering approaches that seek to replace essential genes with orthologs.
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