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首页> 外文期刊>Molecular and Cellular Biology >Induction of pseudohyphal growth by overexpression of PHD1, a Saccharomyces cerevisiae gene related to transcriptional regulators of fungal development.
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Induction of pseudohyphal growth by overexpression of PHD1, a Saccharomyces cerevisiae gene related to transcriptional regulators of fungal development.

机译:通过过表达PHD1来诱导假菌丝生长,PHD1是一种与真菌发育的转录调节因子有关的酿酒酵母基因。

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摘要

When starved for nitrogen, MATa/MAT alpha cells of the budding yeast Saccharomyces cerevisiae undergo a dimorphic transition to pseudohyphal growth. A visual genetic screen, called PHD (pseudohyphal determinant), for S. cerevisiae pseudohyphal growth mutants was developed. The PHD screen was used to identify seven S. cerevisiae genes that when overexpressed in MATa/MAT alpha cells growing on nitrogen starvation medium cause precocious and unusually vigorous pseudohyphal growth. PHD1, a gene whose overexpression induced invasive pseudohyphal growth on a nutritionally rich medium, was characterized. PHD1 maps to chromosome XI and is predicted to encode a 366-amino-acid protein. PHD1 has a SWI4- and MBP1-like DNA binding motif that is 73% identical over 100 amino acids to a region of Aspergillus nidulans StuA. StuA regulates two pseudohyphal growth-like cell divisions during conidiophore morphogenesis. Epitope-tagged PHD1 was localized to the nucleus by indirect immunofluorescence. These facts suggest that PHD1 may function as a transcriptional regulatory protein. Overexpression of PHD1 in wild-type haploid strains does not induce pseudohyphal growth. Interestingly, PHD1 overexpression enhances pseudohyphal growth in a haploid strain that has the diploid polar budding pattern because of a mutation in the BUD4 gene. In addition, wild-type diploid strains lacking PHD1 undergo pseudohyphal growth when starved for nitrogen. The possible functions of PHD1 in pseudohyphal growth and the uses of the PHD screen to identify morphogenetic regulatory genes from heterologous organisms are discussed.
机译:当缺乏氮时,发芽酵母酿酒酵母的MATa / MATα细胞会经历双态转变为假菌丝生长。开发了一种视觉遗传筛选方法,称为PHD(假菌丝决定簇),用于酿酒酵母假菌丝生长突变体。 PHD筛选用于鉴定七个酿酒酵母基因,当它们在氮饥饿培养基上生长的MATa / MAT alpha细胞中过度表达时,会导致早熟和异常活跃的假菌丝生长。表征了PHD1,该基因的过表达诱导其在营养丰富的培养基上的侵袭性假菌丝生长。 PHD1定位于XI染色体,并被预测为编码366个氨基酸的蛋白质。 PHD1具有SWI4和MBP1样的DNA结合基序,在构巢曲霉StuA的100个氨基酸上具有73%的同一性。 StuA调节子叶虫形态发生过程中的两个假菌丝生长样细胞分裂。带表位标签的PHD1通过间接免疫荧光定位在细胞核上。这些事实表明,PHD1可能起转录调节蛋白的作用。在野生型单倍体菌株中PHD1的过表达不会诱导假菌丝的生长。有趣的是,由于BUD4基因的突变,PHD1的过表达增强了具有二倍体极性出芽模式的单倍体菌株的假菌丝生长。此外,缺乏氮磷的缺乏PHD1的野生型二倍体菌株会遭受假菌丝的生长。讨论了PHD1在假菌丝生长中的可能功能以及PHD筛查从异源生物识别形态发生调控基因的用途。

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