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Our analysis uncovered that oomycete genomes, emanating from a common ancestor of Stramenopiles that had a rather large genome encoding for ∼10,000 genes, were growing by continuous duplications that predominantly affected ancestral OGs.
However, emerging evidence from several RNA-sequencing studies supports a more complex model, with several operons in a genome encoding for multiple transcription units depending on the condition [ 7, 8].
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More recent high-throughput genomic technologies have now demonstrated that only <2% of the human genome encodes for amino acids in proteins.
The nonsegmented and noninfectious genome encodes for more than 100 genes.
The human genome encodes for over 40 J proteins with specific cellular and subcellular distributions [1].
KSHV genome encodes for a non-coding polyadenylated nuclear RNA (PAN), which is expressed briefly following KSHV infection [45].
The P. vivax genome encodes for more number of such tryptophan-rich proteins than any other malarial species (http://www.plasmodb.org).
Since the human genome encodes for several hundred different microRNAs, they can be expected to regulate thousands of genes [13].
Additionally, Drosophila genome encodes for Gαf which probably represents an insect-specific subfamily of Gα-subunits [11].
Less than 2% of the human genome encodes for proteins, yet a large fraction, recently estimated to 60% to 90% of the genome can be transcribed [1].
The C. raciborskii CS-505 genome encodes for only one hybrid NRPS-PKS pathway, corresponding to the CYN/doCYN biosynthesis cluster.
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