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Exact(14)
Our DNA band shift assay showed that either reduced OxyR protein or oxidized protein can bind both classes of genes.
Examples of both classes of genes have been identified and characterized from many fruit species [ 8, 12- 15].
We found that the ratio A → G/T → C is about 1.4 on the nontemplate strand of both classes of genes (supplementary fig. 5, Supplementary Material online).
Both classes of genes reside in a 4 Mb gene dense region on human chromosome 6 shared with many other immune genes [ 1].
Other strand asymmetries were found in both classes of genes but the degree of the asymmetries was reduced in non-CGI genes.
Similarly, PCR using primers in the putative transcription factor binding sites show that both classes of genes are present in the chaetognath genome.
Similar(46)
The lack of co-expression of pluripotency markers and lineage specific markers at the protein level despite robust co-expression of transcripts of both classes of gene suggests a role for post-translational regulation of expression, perhaps by small RNAs.
As expected, K4-containing expressed genes were significantly more sensitive to DNaseI digestion than both classes of repressed genes in all three cell lines (P < 5.7e-8; Figure 3).
Moreover, IG genes are themselves less prone to non-synonymous substitutions (69.05%) than both classes of disease genes [AD Vs IG (Z score = 5.0125 confidence level = 95%); ID Vs IG (Z score = 2.011 confidence level = 95%)].
Such a rare situation has probably no evolutionary advantage as both classes of rRNA genes are transcribed by different RNA polymerases [ 109].
Intriguingly, both these classes of genes are involved in similar biological processes.
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