Tang Shunxue, Hass Catherine G, Knapp Steven J
Center for Applied Genetic Technologies, The University of Georgia, 111 Riverbend Road, Athens, GA 30602, USA.
Theor Appl Genet. 2006 Sep;113(5):783-99. doi: 10.1007/s00122-006-0321-3. Epub 2006 Aug 9.
The m (Tph(1)) mutation partially disrupts the synthesis of alpha-tocopherol (vitamin E) in sunflower (Helianthus annuus L.) seeds and was predicted to disrupt a methyltransferase activity necessary for the synthesis of alpha- and gamma-tocopherol. We identified and isolated two 2-methyl-6-phytyl-1,4-benzoquinone/2-methyl-6-solanyl-1,4-benzoquinone methyltransferase (MPBQ/MSBQ-MT) paralogs from sunflower (MT-1 and MT-2), resequenced MT-1 and MT-2 alleles from wildtype (m(+) m(+)) and mutant (m m) inbred lines, identified m as a non-lethal knockout mutation of MT-1 caused by the insertion of a 5.2 kb Ty3/gypsy-like retrotransposon in exon 1, and uncovered a cryptic codominant mutation (d) in a wildtype x mutant F(2) population predicted to be segregating for the m mutation only. MT-1 and m cosegregated and mapped to linkage group 1 and MT-1 was not transcribed in mutant homozygotes (m m). The m locus was epistatic to the d locus--the d locus had no effect in m(+) m(+) and m(+) m individuals, but significantly increased beta-tocopherol percentages in m m individuals. MT-2 and d cosegregated, MT-2 alleles isolated from mutant homozygotes (d d) carried a 30 bp insertion at the start of the 5'-UTR, and MT-2 was more strongly transcribed in seeds and leaves of wildtype (d(+) d(+)) than mutant (d d) homozygotes (transcripts were 2.2- to 5.0-fold more abundant in the former than the latter). The double mutant (m m d d) was non-lethal and produced 24-45% alpha- and 55-74% beta-tocopherol (the wildtype produced 96% alpha- and 4% beta-tocopherol). MT-2 compensated for the loss of the MT-1 function, and the MT-2 mutation profoundly affected the synthesis of tocopherols without adversely affecting the synthesis of plastoquinone crucial for normal plant growth and development.
m(Tph(1))突变部分扰乱了向日葵(Helianthus annuus L.)种子中α-生育酚(维生素E)的合成,据预测该突变会扰乱α-和γ-生育酚合成所需的甲基转移酶活性。我们从向日葵中鉴定并分离出两个2-甲基-6-植基-1,4-苯醌/2-甲基-6-茄尼基-1,4-苯醌甲基转移酶(MPBQ/MSBQ-MT)旁系同源基因(MT-1和MT-2),对野生型(m(+) m(+))和突变型(m m)自交系的MT-1和MT-2等位基因进行了重测序,确定m是MT-1的一个非致死性敲除突变,由一个5.2 kb的Ty3/gypsy样逆转座子插入第1外显子所致,并在一个野生型×突变型F(2)群体中发现了一个隐性共显性突变(d),预计该群体仅针对m突变进行分离。MT-1与m共分离并定位到连锁群1,在突变纯合子(m m)中MT-1不转录。m位点对d位点呈上位性——d位点在m(+) m(+)和m(+) m个体中无影响,但在m m个体中显著提高了β-生育酚的百分比。MT-2与d共分离,从突变纯合子(d d)中分离出的MT-2等位基因在5'-UTR起始处有一个30 bp的插入,并且MT-2在野生型(d(+) d(+))种子和叶片中的转录比突变型(d d)纯合子更强(前者的转录本比后者丰富2.2至5.0倍)。双突变体(m m d d)是非致死性的,产生24 - 45%的α-生育酚和55 - 74%的β-生育酚(野生型产生96%的α-生育酚和4%的β-生育酚)。MT-2补偿了MT-1功能的丧失,并且MT-2突变深刻影响了生育酚的合成,而不会对正常植物生长发育至关重要的质体醌的合成产生不利影响。