Department of Biology and Genetics, University of Pennsylvania, Philadelphia, PA 19104.
J Gerontol A Biol Sci Med Sci. 2014 May;69(5):527-31. doi: 10.1093/gerona/glt121. Epub 2013 Aug 14.
Only a few studies, primarily limited to small samples, have examined the relationship between leukocyte telomere length (LTL) data generated by Southern blots, expressed in kilobases, versus quantitative PCR data, expressed in the telomere product/a single gene product (T/S). In the present study, we compared LTL data generated by the two methods in 681 elderly participants (50% African Americans, 50% of European origin, 49.2% women, mean age 73.7±2.9 years) in the Health Aging and Body Composition Study. The correlation between the data generated by the two methods was modest (R (2) = .27). Both methods captured the age effect on LTL and the longer LTL in women than in men. However, only the Southern blot method showed a significantly longer LTL in African Americans than in European decent individuals, which might be attributed to the larger measurement error of the quantitative PCR-based method than the Southern blots.
仅有少数研究(主要限于小样本)探讨了Southern blot 法生成的以千碱基表示的白细胞端粒长度(LTL)数据与以端粒产物/单个基因产物(T/S)表示的定量 PCR 数据之间的关系。在本研究中,我们比较了 681 名老年参与者(50%为非裔美国人,50%为欧洲裔,49.2%为女性,平均年龄 73.7±2.9 岁)中两种方法生成的 LTL 数据。两种方法生成的数据之间的相关性适中(R (2) =.27)。两种方法均捕捉到了年龄对 LTL 的影响以及女性的 LTL 比男性长。然而,只有 Southern blot 法显示非裔美国人的 LTL 明显长于欧洲裔个体,这可能归因于基于定量 PCR 的方法的测量误差大于 Southern blot 法。