Jennings J C, Albee L D, Kolwyck D C, Surber J B, Taylor M L, Hartnell G F, Lirette R P, Glenn K C
Monsanto, 700 Chesterfield Parkway West, Chesterfield, Missouri 63017, USA.
Poult Sci. 2003 Mar;82(3):371-80. doi: 10.1093/ps/82.3.371.
Questions regarding the digestive fate of DNA and protein from transgenic grain have been raised in regard to human consumption and trade of animal products (e.g., meat, milk, and eggs) from farm animals fed transgenic crops. Using highly sensitive, fully characterized analytical methods, fragments of transgenic and endogenous plant DNA, as well as transgenic protein, were not detected in chicken breast muscle samples from animals fed YieldGard Corn Borer Corn event MON 810 (YG). Total DNA was extracted from breast muscle samples from chickens fed for 42 d with a diet including either 55 to 60% YG grain or 55 to 60% conventional corn grain. DNA preparations were analyzed by PCR followed by Southern blot hybridization for the presence of a 211-bp fragment of the Bacillus thuringiensis (Bt) cry1Ab gene and a 213-bp fragment of the endogenous corn gene sh2 (encoding ADP glucose pyrophosphorylase). By using 1 microg of input DNA per reaction, none of the extracted samples was positive for cry1Ab or sh2 at the limit of detection for these PCR assays. A 396-bp fragment of the chicken ovalbumin (ov) gene, used as a positive control, was amplified from all samples showing that the DNA preparations were amenable to PCR amplification. By using a competitive immunoassay with a limit of detection of approximately 60 ng of CrylAb protein per gram of chicken muscle, neither the CrylAb protein nor immunoreactive peptide fragments were detectable in the breast muscle homogenates from chickens fed YG grain.
关于转基因谷物中DNA和蛋白质在消化过程中的命运,已有人就食用转基因作物的农场动物所产动物产品(如肉、奶和蛋)对人类的影响以及此类产品的贸易问题提出疑问。使用高度灵敏、特征明确的分析方法,在喂食了抗玉米螟转基因玉米MON 810(YG)的动物的鸡胸肌肉样本中,未检测到转基因和内源植物DNA片段以及转基因蛋白。从喂食了含55%至60%YG谷物或55%至60%常规玉米谷物日粮42天的鸡的胸肌样本中提取总DNA。通过PCR分析DNA制剂,随后进行Southern印迹杂交,以检测苏云金芽孢杆菌(Bt)cry1Ab基因的211 bp片段和内源玉米基因sh2(编码ADP葡萄糖焦磷酸化酶)的213 bp片段。在每个反应使用1 μg输入DNA的情况下,在这些PCR检测的检测限内,所提取的样本中cry1Ab或sh2均无阳性结果。用作阳性对照的鸡卵清蛋白(ov)基因的396 bp片段,在所有样本中均被扩增出来,表明DNA制剂适合进行PCR扩增。通过使用检测限约为每克鸡肉60 ng Cry1Ab蛋白的竞争性免疫测定法,在喂食YG谷物的鸡的胸肌匀浆中,既未检测到CrylAb蛋白,也未检测到免疫反应性肽片段。