As Orco is a universally expressed gene, the significantly lower expression level of Orco in D. sechellia might have resulted from the normalization process.
Notably, majority of the CNTs were widely expressed across developmental stages albeit exhibiting significantly lower expression, conservation and length compared to partially novel transcripts.
In Elsanta, significantly lower expression was found for red fruits compared to green fruits.
In contrast, translocation t(11 14) was associated with significantly lower expression levels.
Significantly lower expression was found in the cerebellum and pons (Mann-Whitney U-test; *P < 0.05, **P < 0.01, ***P < 0.001).
Comparing gbM to unmethylated genes revealed that gbM genes had significantly lower expression noise than unmethylated genes, using both noise measures (F* and Fʹ, Table 1).
Interestingly, in contrast to hyperdiploidy, t(11 14) was associated with significantly lower expression of IKZF1, IKZF3, and KPNA2 in MM cells (Fig. 3).
Also in the loaded limbs, there was a significantly lower expression of Lef1 in young Sost KO mice at 8 hrs and adult Sost KO mice at 8 hr and 24 hrs compared to LC mice (Fig. 6A).
A significantly lower expression of Lef1 was measured in the loaded limbs of young Sost KO mice at 8 hrs and adult Sost KO mice at 8 hr and 24 hrs compared to LC mice (Fig. 6A).
Indeed, orthologues with conserved gbM between A. thaliana and A. lyrata exhibited significantly lower expression divergence than other genes, and changes in gbM levels tended to have occurred in lowly expressed (presumably functionally less important) genes (Takuno et al. 2017).
For intergenic im-ncRNAs, their average abundances were comparable to mRNAs in seedlings, but subsets exhibited significantly lower expression in senescing leaves.
