Wang Aide, Yamakake Junko, Kudo Hisayuki, Wakasa Yuhya, Hatsuyama Yoshimichi, Igarashi Megumi, Kasai Atsushi, Li Tianzhong, Harada Takeo
Laboratory of Plant Breeding and Genetics, Faculty of Agriculture and Life Science, Hirosaki University, Hirosaki 036-8561, Japan.
Plant Physiol. 2009 Sep;151(1):391-9. doi: 10.1104/pp.109.135822. Epub 2009 Jul 8.
Expression of MdACS1, coding for 1-aminocyclopropane-1-carboxylate synthase (ACS), parallels the level of ethylene production in ripening apple (Malus domestica) fruit. Here we show that expression of another ripening-specific ACS gene (MdACS3) precedes the initiation of MdACS1 expression by approximately 3 weeks; MdACS3 expression then gradually decreases as MdACS1 expression increases. Because MdACS3 expression continues in ripening fruit treated with 1-methylcyclopropene, its transcription appears to be regulated by a negative feedback mechanism. Three genes in the MdACS3 family (a, b, and c) were isolated from a genomic library, but two of them (MdACS3b and MdACS3c) possess a 333-bp transposon-like insertion in their 5' flanking region that may prevent transcription of these genes during ripening. A single nucleotide polymorphism in the coding region of MdACS3a results in an amino acid substitution (glycine-289 --> valine) in the active site that inactivates the enzyme. Furthermore, another null allele of MdACS3a, Mdacs3a, showing no ability to be transcribed, was found by DNA sequencing. Apple cultivars homozygous or heterozygous for both null allelotypes showed no or very low expression of ripening-related genes and maintained fruit firmness. These results suggest that MdACS3a plays a crucial role in regulation of fruit ripening in apple, and is a possible determinant of ethylene production and shelf life in apple fruit.
编码1-氨基环丙烷-1-羧酸合酶(ACS)的MdACS1的表达与成熟苹果(Malus domestica)果实中的乙烯产生水平平行。在此我们表明,另一个成熟特异性ACS基因(MdACS3)的表达比MdACS1表达的起始提前约3周;随着MdACS1表达增加,MdACS3表达随后逐渐下降。由于MdACS3在经1-甲基环丙烯处理的成熟果实中持续表达,其转录似乎受负反馈机制调控。从基因组文库中分离出MdACS3家族的三个基因(a、b和c),但其中两个(MdACS3b和MdACS3c)在其5'侧翼区域有一个333 bp的转座子样插入,这可能会阻止这些基因在成熟过程中转录。MdACS3a编码区的一个单核苷酸多态性导致活性位点的氨基酸替换(甘氨酸-289→缬氨酸),使该酶失活。此外,通过DNA测序发现了MdACS3a的另一个无效等位基因Mdacs3a,它没有转录能力。对两种无效等位基因型纯合或杂合的苹果品种显示成熟相关基因无表达或表达极低,并保持果实硬度。这些结果表明,MdACS3a在苹果果实成熟调控中起关键作用,并且是苹果果实乙烯产生和货架期的一个可能决定因素。