Tong Xin, Campbell John W, Balázsi Gábor, Kay Krin A, Wanner Barry L, Gerdes Svetlana Y, Oltvai Zoltán N
Department of Pathology, Northwestern University, Chicago, IL 60611, USA.
Biochem Biophys Res Commun. 2004 Sep 10;322(1):347-54. doi: 10.1016/j.bbrc.2004.07.110.
Identifying the genes required for the growth or viability of an organism under a given condition is an important step toward understanding the roles these genes play in the physiology of the organism. Currently, the combination of global transposon mutagenesis with PCR-based mapping of transposon insertion sites is the most common method for determining conditional gene essentiality. In order to accelerate the detection of essential gene products, here we test the utility and reliability of a DNA microarray technology-based method for the identification of conditionally essential genes of the bacterium, Escherichia coli, grown in rich medium under aerobic or anaerobic growth conditions using two different DNA microarray platforms. Identification and experimental verification of five hypothetical E. coli genes essential for anaerobic growth directly demonstrated the utility of the method. However, the two different DNA microarray platforms yielded largely non-overlapping results after a two standard deviations cutoff and were subjected to high false positive background levels. Thus, further methodological improvements are needed prior to the use of DNA microarrays to reliably identify conditionally essential genes on genome-scale.
确定生物体在特定条件下生长或存活所需的基因,是迈向了解这些基因在生物体生理学中所起作用的重要一步。目前,全基因组转座子诱变与基于PCR的转座子插入位点定位相结合,是确定条件性基因必需性的最常用方法。为了加速对必需基因产物的检测,我们在此测试了一种基于DNA微阵列技术的方法的实用性和可靠性,该方法用于鉴定在有氧或厌氧生长条件下于丰富培养基中生长的大肠杆菌的条件性必需基因,我们使用了两种不同的DNA微阵列平台。对五个对厌氧生长至关重要的大肠杆菌假定基因的鉴定和实验验证,直接证明了该方法的实用性。然而,经过两个标准差的截止筛选后,这两种不同的DNA微阵列平台产生的结果在很大程度上不重叠,并且存在较高的假阳性背景水平。因此,在使用DNA微阵列可靠地在基因组规模上鉴定条件性必需基因之前,需要进一步改进方法。