粗神经孢子虫的高通量交配试验

K. McCluskey, Rachel L. Yedlin, S. Walker
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摘要

粗神经孢子虫的交配型试验是鉴定菌株的重要方法。由于作为功能基因组学计划的一部分(Colot et al., 2006)开发的大多数敲除突变体几乎没有明显的表型,因此我们开始测试发送给FGSC的所有敲除菌株的交配类型。我们最初的交配型试验方案与Smith(1962)所描述的相似,包括在玉米粉琼脂(Difco)上在15厘米的培养皿中种植蓬松测试菌株(4317或4347)。在线Neurospora协议中也有描述,“如何使用蓬松的测试器来确定交配类型和其他应用”(http://www.fgsc.net/Neurospora/NeurosporaProtocolGuide.htm)。待测试菌株在Vogels minimal (Vogel, 1956)或适当补充的培养基(McCluskey, 2003)上生长,少量分生孢子被转移到网格上的一个点上。使用这种技术,可以在两个板上测试30到40个应变。虽然稳健,但这种技术是劳动密集型的,因为每次接种都要打开培养皿,偶尔的散生孢子可能会混淆结果。
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High throughput mating tests in Neurospora crassa
Mating type tests in Neurospora crassa are an important way to characterize strains. Since most of the knock-out mutants developed as part of the functional genomics program (Colot et al., 2006) have little obvious phenotype we have undertaken to test the mating type of all of the knock-strains that are sent to the FGSC. Our original mating type test protocol is similar to that described by Smith (1962) and involves growing a lawn of the fluffy tester strains (4317 or 4347) on cornmeal agar (Difco) in 15 cm petri plates. This is also described in the online Neurospora protocol, "How to use fluffy testers for determining mating type and for other applications" (http://www.fgsc.net/Neurospora/NeurosporaProtocolGuide.htm). The strains to be tested are grown on Vogels minimal (Vogel, 1956) or appropriately supplemented medium (McCluskey, 2003) and small amounts of conidia are transferred to a spot on a grid. Using this technique, thirty to forty strains can be tested on two plates. While robust, this technique is labor intensive and because the plate is opened for each inoculation there is the possibility that occasional stray conidia could confound the results.
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