Poly_NumtS_430 or HSA_NumtS_587 observed in massively parallel sequencing of the mitochondrial HV1 and HV2 regions

• Published in: Forensic science international : genetics Vol. 59; p. 102717
• Main Authors: Fujii, Koji, Mita, Yusuke, Watahiki, Haruhiko, Fukagawa, Takashi, Kitayama, Tetsushi, Mizuno, Natsuko, Nakahara, Hiroaki, Sekiguchi, Kazumasa
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.07.2022
• Subjects: Forensic DNA analysis; Hypervariable region 1; Massively parallel sequencing; Mitochondrial DNA; Nuclear mitochondrial DNA sequences; Nuclear mitochondrial DNA sequences; Massively parallel sequencing; Mitochondrial DNA; Hypervariable region 1; Forensic DNA analysis
• ISSN: 1872-4973; 1878-0326
• DOI: 10.1016/j.fsigen.2022.102717

An increasing number of studies on massively parallel sequencing of mitochondrial DNA (mtDNA) have been reporting identification of various types of noise or off-target sequences. Herein, we report that an off-target haplotype (sequence length 192 bp) observed in MiSeq data of mtDNA at nucleotide position 16,209–16,400 was likely caused by polymorphic nuclear mitochondrial DNA sequences (NumtS). Buccal DNA samples from Volunteers #001–004 and Control DNA 007 were amplified with our multiplex system of the B (15,998−16,172), C (16,209−16,400), and E (30−289) regions using 2000 copies of mtDNA. A sample index was added using a Nextera XT index kit, and MiSeq Reagent Nano Kit v2 was used in 2 × 251 cycles on a MiSeq FGx. FASTQ files were analyzed by CLC Genomics Workbench 21.0.3. The extracted SAM files were analyzed using our original Excel macro to sum up the read counts as the phased variant calls for each region. An off-target haplotype differing at 19 sites against the revised Cambridge reference sequence was observed in Volunteer #001 (4 in 10 MiSeq data), Volunteer #002 (2 in 9), and Control DNA 007 (6 in 9). In a BLAST search, the sequence of the off-target haplotype matched perfectly to three polymorphic NumtS (Poly_NumtS_430 [KM281528.1], HSA_NumtS_587 [HE613849.1], and nuclear fossil [S80333.1]) and BAC clone of chromosome 11 (AC107937.2). The sequence also matched perfectly to a Filipino mtDNA (KC993973.1) which was inferred as a chimeric sequence of mtDNA and the HSA_NumtS_587. The sequence of the off-target haplotype was not contained in the latest human reference genome sequence (GRCh38.p13). In a phylogenetic tree, the off-target haplotype was genetically distant from modern human mtDNA and not directly connected to them. In conclusion, observed off-target haplotype amplified by our multiplex system was likely caused by Poly_NumtS_430 or HSA_NumtS_587. •Off-target haplotype (192 bp) was observed in MiSeq data of mtDNA in 16,209–16,400.•Two of four individuals and Control DNA 007 generated off-target haplotype.•Off-target haplotype matched to Poly_NumtS_430, HSA_NumtS_587, and others in BLAST.•Off-target haplotype was not contained in human reference sequence (GRCh38.p13).•Off-target haplotype was outside the modern human mtDNA in a phylogenetic tree.