Gibson A W, Wojciechowicz L A, Danzi S E, Zhang B, Kim J H, Hu Z, Michels C A
Department of Biology, Queens College, Flushing, New York 11367, USA.
Genetics. 1997 Aug;146(4):1287-98. doi: 10.1093/genetics/146.4.1287.
We report the sequence of several MAL-activator genes, including inducible, constitutive, and noninducible alleles of MAL23, MAL43, MAL63, and mal64. Constitutive alleles of MAL23 and MAL43 vary considerably from inducible alleles in their C-terminal domain, with many of the alterations clustered and common to both alleles. The 27 alterations from residues 238-461 of Mal43-C protein are sufficient for constitutivity, but the minimal number of alterations needed for the constitutive phenotype could not be determined. The sequence of mal64, a nonfunctional homologue of MAL63, revealed that Mal64p is 85% identical to Mal63p. Two mutations that activate mal64 and cause constitutivity are nonsense mutations resulting in truncated proteins of 306 and 282 residues. We conclude that the C-terminal region of the MAL-activator, from residues 283-470, contains a maltose-responsive negative regulatory domain, and that extensive mutation or deletion of the entire region causes loss of the negative regulatory function. Additionally, certain sequence elements in the region appear to be necessary for efficient induction of the full-length Mal63 activator protein. These studies highlight the role of ectopic recombination as an important mechanism of mutagenesis of the telomere-associated family of MAL loci.
我们报告了几个MAL激活基因的序列,包括MAL23、MAL43、MAL63和mal64的诱导型、组成型和非诱导型等位基因。MAL23和MAL43的组成型等位基因在其C末端结构域与诱导型等位基因有很大差异,许多改变聚集在一起且两种等位基因共有。Mal43-C蛋白第238 - 461位残基的27个改变足以导致组成型表达,但组成型表型所需的最小改变数量无法确定。mal64是MAL63的无功能同源物,其序列显示Mal64p与Mal63p有85%的同一性。激活mal64并导致组成型表达的两个突变是无义突变,产生了306和282个残基的截短蛋白。我们得出结论,MAL激活蛋白的C末端区域,即第283 - 470位残基,包含一个麦芽糖反应性负调控结构域,该区域的广泛突变或缺失会导致负调控功能丧失。此外,该区域的某些序列元件似乎是全长Mal63激活蛋白有效诱导所必需的。这些研究突出了异位重组作为端粒相关MAL基因座家族诱变的重要机制的作用。