Moloney Christina, Rayaprolu Sruti, Howard John, Fromholt Susan, Brown Hilda, Collins Matt, Cabrera Mariela, Duffy Colin, Siemienski Zoe, Miller Dave, Swanson Maurice S, Notterpek Lucia, Borchelt David R, Lewis Jada
Center for Translational Research in Neurodegenerative Disease, University of Florida, Gainesville, FL, USA.
Department of Neuroscience, University of Florida, Gainesville, FL, USA.
Acta Neuropathol Commun. 2017 Dec 13;5(1):97. doi: 10.1186/s40478-017-0502-0.
The authors are retracting this article. The article describes mice expressing wild-type human MATR3. However, since publication the authors have become aware that all of the lines of mice described express human MATR3 containing the F115C mutation. Transgenic mice expressing wild-type and mutant Matrin were created simultaneously in their laboratory and, at a crucial stage of generating the DNA for embryo injection, as confirmed by an investigation by the University of Florida, the DNA preparations were accidentally mislabelled. All of the founders created were mosaic, requiring extensive breeding to isolate stable lines. Mice mislabelled as expressing wild-type MATR3 were the first to produce lines that stably transmitted the transgene and thus were the first to be characterized. However, as lines of mice that were mislabelled as expressing the mutant (F115C) MATR3 were ultimately established, the data began to suggest that an error had been made. Sequence analysis of amplified tail DNA from mice descended from the lines reported in the article have revealed that they express the F115C variant. The data described are therefore an accurate description of the pathology of mice that express the F115C variant of MATR3, but not of mice expressing wild-type MATR3. The authors are preparing a new manuscript reporting data from both mice expressing the F115C variant of MATR3 and mice expressing wild-type MATR3.
作者们正在撤回本文。本文描述了表达野生型人类MATR3的小鼠。然而,自发表以来,作者们意识到文中所描述的所有小鼠品系均表达含有F115C突变的人类MATR3。表达野生型和突变型Matrin的转基因小鼠是在他们的实验室同时创建的,并且正如佛罗里达大学调查所证实的,在为胚胎注射制备DNA的关键阶段,DNA制剂被意外错误标记。所有创建的奠基小鼠都是嵌合体,需要广泛繁殖以分离出稳定的品系。被错误标记为表达野生型MATR3的小鼠是最先产生稳定传递转基因的品系的,因此也是最先被鉴定的。然而,随着被错误标记为表达突变型(F115C)MATR3的小鼠品系最终得以建立,数据开始表明出现了错误。对本文报道的品系所衍生的小鼠的扩增尾部DNA进行序列分析后发现,它们表达的是F115C变体。因此,所描述的数据准确地描述了表达MATR3的F115C变体的小鼠的病理学情况,但并非表达野生型MATR3的小鼠的情况。作者们正在准备一篇新的稿件,报告表达MATR3的F115C变体的小鼠和表达野生型MATR3的小鼠的数据。