Bisulfite Amplicon Sequencing Can Detect Glia and Neuron Cell-Free DNA in Blood Plasma

oleh: Zac Chatterton, Zac Chatterton, Zac Chatterton, Zac Chatterton, Zac Chatterton, Natalia Mendelev, Natalia Mendelev, Natalia Mendelev, Natalia Mendelev, Sean Chen, Sean Chen, Sean Chen, Sean Chen, Walter Carr, Walter Carr, Gary H. Kamimori, Yongchao Ge, Andrew J. Dwork, Andrew J. Dwork, Andrew J. Dwork, Fatemeh Haghighi, Fatemeh Haghighi, Fatemeh Haghighi, Fatemeh Haghighi

Format: Article
Diterbitkan: Frontiers Media S.A. 2021-07-01

Deskripsi

Sampling the live brain is difficult and dangerous, and withdrawing cerebrospinal fluid is uncomfortable and frightening to the subject, so new sources of real-time analysis are constantly sought. Cell-free DNA (cfDNA) derived from glia and neurons offers the potential for wide-ranging neurological disease diagnosis and monitoring. However, new laboratory and bioinformatic strategies are needed. DNA methylation patterns on individual cfDNA fragments can be used to ascribe their cell-of-origin. Here we describe bisulfite sequencing assays and bioinformatic processing methods to identify cfDNA derived from glia and neurons. In proof-of-concept experiments, we describe the presence of both glia- and neuron-cfDNA in the blood plasma of human subjects following mild trauma. This detection of glia- and neuron-cfDNA represents a significant step forward in the translation of liquid biopsies for neurological diseases.