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[具体物种名称]中的自然变异及[相关基因或因素名称]是[具体物种名称]中特定条件下生长缺陷的基础。 (你提供的原文不完整,缺少关键信息,这里是根据格式进行的大致补充翻译)

Natural Variation in and Underlie Condition-Specific Growth Defects in .

作者信息

Sirr Amy, Scott Adrian C, Cromie Gareth A, Ludlow Catherine L, Ahyong Vida, Morgan Trey S, Gilbert Teresa, Dudley Aimée M

机构信息

Pacific Northwest Research Institute, Seattle, Washington 98122.

Department of Molecular and Cellular Biology, University of California, Berkeley, California 94720.

出版信息

G3 (Bethesda). 2018 Jan 4;8(1):239-251. doi: 10.1534/g3.117.300392.

DOI:10.1534/g3.117.300392
PMID:29138237
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5765352/
Abstract

Despite their ubiquitous use in laboratory strains, naturally occurring loss-of-function mutations in genes encoding core metabolic enzymes are relatively rare in wild isolates of Here, we identify a naturally occurring serine auxotrophy in a sake brewing strain from Japan. Through a cross with a honey wine (white tecc) brewing strain from Ethiopia, we map the minimal medium growth defect to , which encodes 3-phosphoserine aminotransferase and is orthologous to the human disease gene, To investigate the impact of this polymorphism under conditions of abundant external nutrients, we examine growth in rich medium alone or with additional stresses, including the drugs caffeine and rapamycin and relatively high concentrations of copper, salt, and ethanol. Consistent with studies that found widespread effects of different auxotrophies on RNA expression patterns in rich media, we find that the loss-of-function allele dominates the quantitative trait locus (QTL) landscape under many of these conditions, with a notable exacerbation of the effect in the presence of rapamycin and caffeine. We also identify a major-effect QTL associated with growth on salt that maps to the gene encoding the sodium exporter, We demonstrate that the salt phenotype is largely driven by variation in the promoter, which harbors a deletion that removes binding sites for the Mig1 and Nrg1 transcriptional repressors. Thus, our results identify natural variation associated with both coding and regulatory regions of the genome that underlie strong growth phenotypes.

摘要

尽管它们在实验室菌株中被广泛使用,但编码核心代谢酶的基因中自然发生的功能丧失突变在野生分离株中相对罕见。在这里,我们在一株来自日本的清酒酿造菌株中鉴定出一种自然发生的丝氨酸营养缺陷型。通过与一株来自埃塞俄比亚的蜂蜜酒(白泰克)酿造菌株杂交,我们将基本培养基生长缺陷定位到一个基因,该基因编码3-磷酸丝氨酸转氨酶,并且与人类疾病基因同源。为了研究这种多态性在丰富外部营养条件下的影响,我们单独检测了在丰富培养基中的生长情况,或检测了在包括咖啡因和雷帕霉素以及相对高浓度的铜、盐和乙醇等附加应激条件下的生长情况。与发现不同营养缺陷型对丰富培养基中RNA表达模式有广泛影响的研究一致,我们发现在许多这些条件下,功能丧失等位基因在数量性状位点(QTL)图谱中占主导地位,在雷帕霉素和咖啡因存在的情况下,这种影响会显著加剧。我们还鉴定出一个与在盐上生长相关的主效QTL,它定位到编码钠输出蛋白的基因。我们证明盐表型在很大程度上是由该基因启动子的变异驱动的,该启动子存在一个缺失,去除了Mig1和Nrg1转录抑制因子的结合位点。因此,我们的结果鉴定出与基因组的编码区和调控区相关的自然变异,这些变异是强大生长表型的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858b/5765352/29be1bb775c9/239f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858b/5765352/e455e0a7f024/239f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858b/5765352/ec6f2f716e32/239f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858b/5765352/52558714c3f2/239f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858b/5765352/78fab4a82440/239f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858b/5765352/118a03205210/239f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858b/5765352/29be1bb775c9/239f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858b/5765352/e455e0a7f024/239f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858b/5765352/ec6f2f716e32/239f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858b/5765352/52558714c3f2/239f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858b/5765352/78fab4a82440/239f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858b/5765352/118a03205210/239f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/858b/5765352/29be1bb775c9/239f6.jpg

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