Casas-Vila Núria, Scheibe Marion, Freiwald Anja, Kappei Dennis, Butter Falk
Quantitative Proteomics, Institute of Molecular Biology (IMB) gGmbH, Ackermannweg 4, 55128, Mainz, Germany.
Cancer Science Institute of Singapore, National University of Singapore, 14 Medical Drive, 117599, Singapore, Singapore.
BMC Genomics. 2015 Nov 17;16:965. doi: 10.1186/s12864-015-2158-0.
To date, telomere research in fungi has mainly focused on Saccharomyces cerevisiae and Schizosaccharomyces pombe, despite the fact that both yeasts have degenerated telomeric repeats in contrast to the canonical TTAGGG motif found in vertebrates and also several other fungi.
Using label-free quantitative proteomics, we here investigate the telosome of Neurospora crassa, a fungus with canonical telomeric repeats. We show that at least six of the candidates detected in our screen are direct TTAGGG-repeat binding proteins. While three of the direct interactors (NCU03416 [ncTbf1], NCU01991 [ncTbf2] and NCU02182 [ncTay1]) feature the known myb/homeobox DNA interaction domain also found in the vertebrate telomeric factors, we additionally show that a zinc-finger protein (NCU07846) and two proteins without any annotated DNA-binding domain (NCU02644 and NCU05718) are also direct double-strand TTAGGG binders. We further find two single-strand binders (NCU02404 [ncGbp2] and NCU07735 [ncTcg1]).
By quantitative label-free interactomics we identify TTAGGG-binding proteins in Neurospora crassa, suggesting candidates for telomeric factors that are supported by phylogenomic comparison with yeast species. Intriguingly, homologs in yeast species with degenerated telomeric repeats are also TTAGGG-binding proteins, e.g. in S. cerevisiae Tbf1 recognizes the TTAGGG motif found in its subtelomeres. However, there is also a subset of proteins that is not conserved. While a rudimentary core TTAGGG-recognition machinery may be conserved across yeast species, our data suggests Neurospora as an emerging model organism with unique features.
迄今为止,尽管与脊椎动物以及其他几种真菌中发现的典型TTAGGG基序相比,酿酒酵母和裂殖酵母的端粒重复序列已经退化,但真菌中的端粒研究主要集中在这两种酵母上。
我们使用无标记定量蛋白质组学方法,研究了具有典型端粒重复序列的真菌粗糙脉孢菌的端粒体。我们发现,在我们的筛选中检测到的至少六种候选蛋白是直接与TTAGGG重复序列结合的蛋白质。虽然其中三个直接相互作用蛋白(NCU03416 [ncTbf1]、NCU01991 [ncTbf2] 和 NCU02182 [ncTay1])具有在脊椎动物端粒因子中也发现的已知的myb/同源框DNA相互作用结构域,但我们还表明,一种锌指蛋白(NCU07846)和两种没有任何注释的DNA结合结构域的蛋白质(NCU02644和NCU05718)也是双链TTAGGG的直接结合蛋白。我们还发现了两种单链结合蛋白(NCU02404 [ncGbp2] 和 NCU07735 [ncTcg1])。
通过无标记定量相互作用组学,我们在粗糙脉孢菌中鉴定出了TTAGGG结合蛋白,这表明通过与酵母物种的系统基因组比较,端粒因子的候选蛋白得到了支持。有趣的是,端粒重复序列退化的酵母物种中的同源物也是TTAGGG结合蛋白,例如在酿酒酵母中,Tbf1识别其亚端粒中发现的TTAGGG基序。然而,也有一部分蛋白质并不保守。虽然一个基本的核心TTAGGG识别机制可能在酵母物种中是保守的,但我们的数据表明粗糙脉孢菌是一种具有独特特征的新兴模式生物。