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. Author manuscript; available in PMC: 2012 Jul 1.
Published in final edited form as: Biotechnol Bioeng. 2011 Mar 11;108(7):1651–1661. doi: 10.1002/bit.23092

Table 2.

Refined set of mmu-miR-466h possible targets. Table shows possible binding site(s) of mmu-miR-466h seed region(s) and mRNA 3′-UTRs of the respective target gene. Brief description of the known anti-apoptotic roles for those genes is given

Mouse gene symbol mmu-miR-466h binding site(s) in mRNA 3′-UTR (miR-466h binding nucleotides #) Anti-apoptotic role of targeted gene
bcl2 GCACAC (2–7) Bcl2 is outer mitochondrial membrane protein which suppresses apoptosis either by preventing release of cytochrome C from mitochondria or by binding apoptosis activating factor (Apaf-1)
bcl2l2 GCACAC(2–7)
TGCACA(3–8)
Bcl2l2 (bcl-w) inhibits formation of permeability transition pore and subsequent release of cytochrome C by binding to bax
birc6 GCACA (3–7) Birc6 (BRUCE, Apollon) can inhibit apoptosome by binding to Caspase-9 and occupying its active-site pocket. It can function as E2 ubiquitin conjugase for Caspase-9 and Smac/Diablo. Also, in response to loss of BIRC6 function p53 activates PIDD/Caspase-2 and bax/bak resulting in mitochondrial apoptosis
cflar TGCACAC(2–8), 3 of TGCACA(3–8)
GCACAC (2–7)
Caspase-8 and FADD-like apoptosis regulator. Acts as an inhibitor of TNFRSF6 mediated apoptosis. It inhibits procaspase-8 cleavage and Caspase-8 activation.
dad1 2 of TGCACA (3–8) Defender against cell death1. It is a component of N-oligosaccharyl transferase catalyzing transfer of oligosaccharide from lipid-linked donor to nascent polypeptide chain. Loss of dad1 was reported to trigger apoptosis
naip7 2 of GCACAC(2–7) Naip7 (birc1g) Baculoviral iap repeat-containing 1g protein. BIR domains are known to inhibit apoptosis by direct inhibition of the caspase family of proteases
smo TGCACAC (2–8)
GCACAC (2–7)
Part of Hedgehog signaling pathway. Activated smo uninhibits gli-1 transcriptional factor which stimulates up-regulation of bcl2
stat5a GCACAC (2–7) Part of Jak-Stat signaling pathway. Stat5a dimers are transcriptional factors for bcl-xL and bcl2 genes
tegt TGCACAC (2–8) Tegt is a multipass membrane protein. Interacts with bcl2 and bcl-xL and inhibits bax