Hello all, I observed that different gene id can have their position been overlapped. For example, ENSG00000167244
starts at 2129112 and ends at 2141238 (I took min of start and max of end for all line w.r.t. ENSG00000167244
), while ENSG00000240801
starts at 2129121 and ends at 2129964, or ENSG00000284779
starts at 2129112 and ends at 2158391. They are all on strand "-" and same chromosome 11. These information is derived from annotation file (gtf) of cell ranger.
chr11 HAVANA gene 2129112 2141238 . - . gene_id "ENSG00000167244"; gene_version "21"; gene_type "protein_coding"; gene_name "IGF2"; level 2; hgnc_id "HGNC:5466"; tag "ncRNA_host"; tag "overlapping_locus"; havana_gene "OTTHUMG00000009395.13";
chr11 HAVANA gene 2129121 2129964 . - . gene_id "ENSG00000240801"; gene_version "1"; gene_type "lncRNA"; gene_name "AC132217.1"; level 2; tag "overlapping_locus"; havana_gene "OTTHUMG00000009394.2";
Can anyone help to explain the reason behind this behaviour?
I'm trying to calculate distance of between position of interest (ex: 2129149) and start of gene that this position of interest lies on. However, these overlaps confuse me.
LIFE : https://pubmed.ncbi.nlm.nih.gov/26613890/
I like the descriptions of proximal causes much more than explanations by ultimate causes :)
Can you share a little more about proximal causes? I try to search but find nothing.
my 2 cents.
The linked paper is not free, but i found this part of the abstract quite interesting:
the last paragraph states that overlapping transcriptions confer high plasticity to eukaryotic genomes (this could be seen as a proximal cause) that represent an evolutionary advantage that explains the reason (of the existence) of such phenomenon, the ultimate cause.
Ohh good point.
Thanks for your reference. Honestly, I try to walk through the paper but barely get its idea. It's because I don't have background in biology. But from this I can have some keywords for searching further.