Description and display conventions

NumtS (Nuclear mitochondrial sequences) are mitochondrial fragments inserted in nuclear genomic sequences. The most credited hypothesis concerning their generation suggests that in presence of mutagenic agents, or under stress conditions, fragments of mtDNA escape from mitochondria, reach the nucleus and insert into chromosomes during break repair; although NumtS can also derive from duplication of genomic fragments. NumtS may be a cause of contamination during mtDNA sequencing and hence frequent false low heteroplasmic evidences have been reported. The Bioinformatics group chaired by M. Attimonelli (University of Bari, Italy) has produced the RPNumtS (Reference Pig NumtS) compilation annotating Pig assembled NumtS. To allow the scientific community to access the compilation and to perform genomics comparative analyses inclusive of the NumtS data, the group has designed the Pig NumtS tracks described below.

The NumtS tracks show nuclear and mitochondrial regions, based on the High Score Pairs (HSPs) obtained by aligning the mitochondrial reference genome (NC_012095) with the susScr2 assembly of the pig genome.

  1. "NumtS (Nuclear mitochondrial Sequences)" Track

    The "NumtS mitochondrial sequences" track shows the mapping of the HSPs returned by BlastN on the nuclear genome. The shading of the items reflect the similarity returned by BlastN, and the direction of the arrows is concordant with the strand of the alignment. For every item, a link pointing to the mitochondrial mapping is provided, thus allowing a fast cross among the NumtS genomic contexts.

  2. "NumtS assembled" Track

    The "NumtS assembled" track shows items obtained by assembling HSPs annotated in the "NumtS" track fulfilling the following conditions:

    Exceptions for the second condition arise when a long repetitive element is present between two HSPs.

  3. "NumtS on mitochondrion" Track

    The "NumtS on mitochondrion" track shows the mapping of the HSPs on the mitochondrial genome. The shading of the items reflects the similarity returned by BlastN, and the direction of the arrows is concordant with the strand of the alignment. For every item, a link pointing to the nuclear mapping is provided.

  4. "Pig NumtS on mitochondrion SNP" Track

    The "Pig NumtS SNP" shows the mapping of the HSPs on the mitochondrial genome, with the SNPs which fall within, derived from comparison with the susScr2 assembly. No shading is here provided. For every item, a link pointing to the nuclear mapping is provided.

Methods

NumtS mappings were obtained by running Blast2seq (program: BlastN) between each chromosome of the Pig Genome (susScr2 assembly) and the Pig mitochondrial reference sequence (AC: NC_012095), fixing the e-value threshold to 1e-03. The assembling of the HSPs was performed with spreadsheet interpolation and manual inspection. BED format is used for the first three annotation tracks, while for the last one the SAM/BAM format is preferred.

Credits

These data were provided by Francesco Maria Calabrese, Dario Leonardo Balacco, Domenico Simone and Marcella Attimonelli from the Department of of Biosciences, Biotechnology and Pharmacological Sciences (University of Bari, Italy). Manual inspection and format details have been carried out by Francesco Maria Calabrese, Dario Leonardo Balacco and Domenico Simone.

References

Calabrese FM, Simone D, Attimonelli M. Primates and mouse NumtS in the UCSC Genome Browser. BMC Bioinformatics. 2012 Mar 28;13 Suppl 4:S15. doi: 10.1186/1471-2105-13-S4-S15. PMID: 22536961 PMCID: PMC3314570

Simone D, Calabrese FM, Lang M, Gasparre G, Attimonelli M. The reference human nuclear mitochondrial sequences compilation validated and implemented on the UCSC genome browser. BMC Genomics. 2011 Oct 20;12:517. doi: 10.1186/1471-2164-12-517. PMID: 22013967 PMCID: PMC3228558

Lascaro D, Castellana S, Gasparre G, Romeo G, Saccone C, Attimonelli M. The RHNumtS compilation: features and bioinformatics approaches to locate and quantify Human NumtS. BMC Genomics. 2008 Jun 3;9:267. doi: 10.1186/1471-2164-9-267. PMID: 18522722 PMCID: PMC2447851