4.2 Article

Establishing a reference dataset for the authentication of spinal muscular atrophy cell lines using STR profiling and digital PCR

Journal

NEUROMUSCULAR DISORDERS
Volume 27, Issue 5, Pages 439-446

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.nmd.2017.02.002

Keywords

Spinal muscular atrophy; Cell line authentication; Short tandem repeat profiling; Digital PCR; SMN1; SMN2

Funding

  1. National Institute of General Medical Sciences of the National Institutes of Health (NIH) Institutional Development Award (IDeA) Centers of Biomedical Research Excellence [P20GM103464, P30GM114736]
  2. IDeA Networks of Biomedical Research Excellence [P20GM103446]
  3. Nemours Foundation
  4. NIH [R01HD054599, U54HD079123-01A1]

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Fibroblasts and lymphoblastoid cell lines (LCLs) derived from individuals with spinal muscular atrophy (SMA) have been and continue to be essential for translational SMA research. Authentication of cell lines helps ensure reproducibility and rigor in biomedical research. This quality control measure identifies mislabeling or cross-contamination of cell lines and prevents misinterpretation of data. Unfortunately, authentication of SMA cell lines used in various studies has not been possible because of a lack of a reference. In this study, we provide said reference so that SMA cell lines can be subsequently authenticated. We use short tandem repeat (STR) profiling and digital PCR (dPCR), which quantifies SMN1 and SMN2 copy numbers, to generate molecular identity codes for fibroblasts and LCLs that are commonly used in SMA research. Using these molecular identity codes, we clarify the familial relationships within a set of fibroblasts commonly used in SMA research. This study presents the first cell line reference set for the SMA research community and demonstrates its usefulness for re-identification and authentication of lines commonly used as in vitro models for future studies. (C) 2017 Elsevier B.V. All rights reserved.

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