Hi all,
I am working on assembling the mitochondrial genome of my insect parasitoid, Microctonus aethiopoides. There is a reference mitochondrial genome of Microctonus brassicae available in NCBI (accession number: OU953852) with a size of 40kbp. Using this as a reference, I assembled the Nanopore long-read data with Flye in meta mode and obtained a contig of 31kbp with coverage >600x, and the assembly is circular according to the Flye info file. (Note : Used this method because non of the mito genome assembly tools (Novoplasty, Mitofinder, Mitoz, mitoflow) could produce a circular contig)
For additional confirmation, I blasted this contig against the nucleotide database (ntdb) and got max hits for mitochondrial genomes, confirming that it is indeed the mitochondrial genome.
Here are my questions:
Is it common for insect mitochondrial genomes to be as large as 30-40kbp? I was initially shocked to see the reference in NCBI with 40kbp, as I understood that mitochondrial genomes typically range from 15-25kbp.
Could the large size be due to many repeat regions? When visualizing the mapped regions in IGV, I noticed many reads with low mapping quality, which might indicate repeat regions. How should I deal with these repeats?
Annotation issues: After annotating this assembled genome, it annotated mitochondrial genes but also many OH (origin of replication) regions. Is this normal, and how should I address this in my analysis?
Any suggestions or insights would be greatly appreciated!
Thanks for your suggestion. Actually coverage across the mitogenome is almost uniform infact it's higher (as in picture) than what we expect in nuclear gneome (Guess that confirms it is mitogenome)