Wieser J, Adams T H
Department of Biology, Texas A&M University, College Station 77843.
Genes Dev. 1995 Feb 15;9(4):491-502. doi: 10.1101/gad.9.4.491.
The timing of asexual fruiting body formation during Aspergillus nidulans colony development is precisely regulated so that conidiophores are typically produced 1-2 mm behind the growing edge of the colony. Mutations in any of four A. nidulans genes, flbB, flbC, flbD, or flbE, result in colonies that are delayed at least 24 hr in their ability to initiate conidiophore development resulting in fluffy colonies with conidiophores forming in the center, at least 12-15 mm behind the growing edge. The requirement for each of these four genes in determining the timing of developmental initiation precedes transcriptional activation of the primary developmental regulatory gene brlA, indicating a possible role for each gene in developmentally regulated activation of brlA expression. The wild-type flbD gene was isolated and shown to encode an approximately 1.6-kb mRNA that is present throughout the A. nidulans life cycle. The deduced FlbD protein sequence predicts a 314-amino-acid polypeptide with significant identity at its amino terminus to the DNA-binding domain of the Myb family of transcription factors indicating that FlbD probably functions as a sequence-specific transcriptional activator. Although conidiophore development does not normally occur in submerged culture, forced overexpression of flbD in submerged hyphae caused inappropriate activation of brlA expression and resulted in production of complex conidiophores that produced all of the distinct cell types observed in wild-type conidiophores including viable spores. This ability of flbD overexpression to activate conidiation requires brlA, flbB, and flbA (another early developmental regulator) but does not require flbC or flbE. We propose that FlbD functions during normal development by activating transcription of other genes required for development (such as brlA) and that FlbD activity is normally controlled post-transcriptionally by an unknown mechanism.
在构巢曲霉菌落发育过程中,无性产果体形成的时间受到精确调控,使得分生孢子梗通常在菌落生长边缘后方1 - 2毫米处产生。构巢曲霉的四个基因flbB、flbC、flbD或flbE中任何一个发生突变,都会导致菌落在启动分生孢子梗发育的能力上至少延迟24小时,从而形成蓬松的菌落,分生孢子梗在菌落中心形成,至少在生长边缘后方12 - 15毫米处。这四个基因中的每一个在决定发育起始时间方面的需求都先于主要发育调控基因brlA的转录激活,这表明每个基因在brlA表达的发育调控激活中可能发挥作用。野生型flbD基因被分离出来,结果显示它编码一种约1.6千碱基的信使核糖核酸,在构巢曲霉的整个生命周期中都存在。推导出来的FlbD蛋白序列预测其为一个314个氨基酸的多肽,其氨基末端与转录因子Myb家族的DNA结合结构域具有显著的同源性,这表明FlbD可能作为一种序列特异性转录激活因子发挥作用。尽管在液体培养中通常不会发生分生孢子梗的发育,但在液体菌丝中强制过表达flbD会导致brlA表达的不适当激活,并导致产生复杂的分生孢子梗,这些分生孢子梗产生了在野生型分生孢子梗中观察到的所有不同细胞类型,包括有活力的孢子。flbD过表达激活产孢的这种能力需要brlA、flbB和flbA(另一个早期发育调节因子),但不需要flbC或flbE。我们提出,FlbD在正常发育过程中通过激活其他发育所需基因(如brlA)的转录来发挥作用,并且FlbD的活性通常通过一种未知机制在转录后受到控制。