Meyer-Bothling L E, Polacco J C, Cianzio S R
Department of Biochemistry, 117 Schweitzer Hall, University of Missouri, Columbia, MO 65211, USA.
Mol Gen Genet. 1987 Oct;209(3):432-8. doi: 10.1007/BF00331146.
Two new soybean [Glycine max (L.) Merr. cv. Williams] loci, designated Eu2 and Eu3, were identified in which ethyl methanesulfonate (EMS)-induced mutation eliminated urease activity. These loci showed no linkage to each other or to the "Sun-Eul" locus described in the accompanying paper (Meyer-Bothling and Polacco 1987). Unlike sun (seed urease-null) mutations those at Eu2 and Eu3 affected both urease isozymes: the embryo-specific (seed) and the ubiquitous (leaf) urease. The eu2/eu2 mutant had no leaf activity and 0.6% normal seed activity. Two mutant Eu3 alleles were recovered, eu3-e1 and Eu3-e3. The eu3-e1/eu3-e1 genotype lacked both activities while Eu3-e3/Eu3-e3 had coordinately reduced leaf (0.1%) and seed (0.1%) activities. Only the Eu3-e3 mutation showed partial dominance, yielding about 5%-10% normal activity for each urease in the heterozygous state. Each homozygous mutant contained normal levels of embryo-specific urease mRNA and protein subunit, both of normal size. However, urease polymerization was aberrant in all three mutants. In all cases where urease could be measured, it was found to be temperature sensitive and, in addition, the embryo-specific urease of Eu3-e3/Eu3-e3 had an altered pH dependence. These mutants may be defective in a urease maturation function common to both isozymes as suggested by the normal levels of urease gene product, coordinately (or nearly so) reduced urease isozyme activities, temperature sensitivity in both ureases (Eu3-e3) and the non-linkage of Eu2 and Eu3 to the locus encoding embryo-specific urease (Sun-Eul). Ubiquitous urease activity is reduced in mutant seed coat and callus culture as well as in leaf and cotyledon tissue. No mutant callus utilized urea (5 to 10 nM0 as sole nitrogen source. However, all mutant cell lines tolerated normally toxic levels of urea (25 to 250 mM) added to medium containing KNO3/NH4No3 as nitrogen source. Urea thus may be used in cell culture as a selection agent for phenotypes either lacking or regaining an active ubiquitous urease.
在大豆[Glycine max (L.) Merr. cv. Williams]中鉴定出两个新位点,命名为Eu2和Eu3,其中甲磺酸乙酯(EMS)诱导的突变消除了脲酶活性。这些位点彼此之间以及与随附论文(Meyer - Bothling和Polacco,1987年)中描述的“Sun - Eul”位点均无连锁关系。与sun(种子脲酶缺失)突变不同,Eu2和Eu3位点的突变影响了两种脲酶同工酶:胚胎特异性(种子)脲酶和普遍存在的(叶片)脲酶。eu2/eu2突变体叶片中无脲酶活性,种子中脲酶活性为正常水平的0.6%。获得了两个突变的Eu3等位基因,eu3 - e1和Eu3 - e3。eu3 - e1/eu3 - e1基因型两种活性均缺失,而Eu3 - e3/Eu3 - e3基因型的叶片(0.1%)和种子(0.1%)脲酶活性协同降低。只有Eu3 - e3突变表现出部分显性,杂合状态下每种脲酶的活性约为正常活性的5% - 10%。每个纯合突变体中胚胎特异性脲酶mRNA和蛋白质亚基水平正常,大小也正常。然而,在所有三个突变体中脲酶的聚合均异常。在所有能够检测脲酶的情况下,发现其对温度敏感,此外,Eu3 - e3/Eu3 - e3的胚胎特异性脲酶对pH的依赖性也发生了改变。鉴于脲酶基因产物水平正常、脲酶同工酶活性协同(或近乎协同)降低、两种脲酶(Eu3 - e3)对温度敏感以及Eu2和Eu3与编码胚胎特异性脲酶的位点(Sun - Eul)无连锁关系,这些突变体可能在两种同工酶共有的脲酶成熟功能上存在缺陷。在突变体种皮、愈伤组织培养物以及叶片和子叶组织中,普遍存在的脲酶活性均降低。没有突变愈伤组织能够利用尿素(5至10 nM)作为唯一氮源。然而,所有突变细胞系都能耐受添加到以KNO3/NH4NO3作为氮源的培养基中的正常毒性水平的尿素(25至250 mM)。因此,尿素可在细胞培养中用作选择剂,用于筛选缺乏或恢复活性普遍存在的脲酶的表型。