Ψ MOGAT2 - Pteropus vampyrus

Reference Gene:
Job_ID:
Curator:
GlossID Species Gene Loss Mechanism Loss Type Lineage Specific Evidence Accession Nr.
GL_SMB56E Pteropus vampyrus LOF (frameshift, premature stop, ss) Full No Genomic

Statements

Type Excerpt DOI
Methodology & Validation "For a gene to be classified as lost, we require that a lineage, which descends from an ancestor with an intact gene, exhibits several gene-inactivating mutations that most likely result in a non-functional protein. As gene-inactivating mutations, we consider frameshifting insertions and deletions, inframe stop codon mutations, and splice site-disrupting mutations. In addition, we consider the loss of exons or even entire genes, which could occur due to either large deletions in the genome or the accumulation of numerous mutations that destroy any sequence similarity. For all previously unknown gene losses presented here, we further confirmed the loss by validating the gene-inactivating mutations with unassembled sequencing reads from the respective species." 10.1038/s41467-018-03667-1
Timing of Loss "Several shared inactivating mutations (asterisks) show that the loss of MOGAT2 already happened in the ancestor of both fruit bats." 10.1038/s41467-018-03667-1
Phenotypic "MOGAT2, which is predominantly expressed in the small intestine in mice plays a major role in the absorption of dietary fat." 10.1038/s41467-018-03667-1
Other "The loss of this enzyme is likely a consequence of the fat poor diet of frugivorous bats." 10.1038/s41467-018-03667-1

Curator Observations

Sup Figure 13 & 26; Sup Table 4