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Even though not all yeast SL pairs are expected to be conserved in distant organisms, those associated to essential functions have a higher conservation probability.
RP1L1 was found to be conserved in distant vertebrates [ 8].
These findings raise questions as to why microsatellites might be conserved in distant species, and why microsatellites in different genomic locations are maintained to different extents.
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Clear orthologs of non-classical class I are conserved in distant marsupial lineages.
We show that this dual osa-miR159a.2-osa-miR159a.1 structure is conserved in distant rice species and maize.
For example, Glutamate receptors (7tm_3) have protein domain configurations that are conserved in distant eukaryotic lineages, including those with Venus Flytrap module (ANF_receptor), OpuAC, or Bmp domains (fig. 3).
A subsequent, conceptually similar comparison of introns whose position is conserved in distant eukaryotic lineages (e.g., plants and animals) – old introns, and lineage-specific, young introns in a carefully curated gene set produced nearly identical results[ 23].
Third, we were interested to see if the diametrically opposed TE composition of C. elegans and D. melanogaster would be conserved in their distant relatives.
By contrast, the regulation model predicts that the NMD-specific exons should be under purifying selection and that the NMD regulation of orthologous genes be conserved in relatively distant species.
In each group, potential functional motifs are conserved in phylogenetically distant species, including foodborne pathogens and probiotic strains.
Given that the function of the Csm1/Lrs4 complex is conserved in two distant yeast species, it is likely that a similar complex is employed to prevent merotelic attachment in higher eukaryotes.
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