Searching journal content for articles similar to Murchison et al. 18 (6): 995.

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  1. ...that snoRNAs rely on conserved motifs, a stable global structure and terminal stem, and a transcribed locus to be expressed. We observe that these features explain well the varying abundance of snoRNAs embedded within the same host gene. By predicting the expression status of snoRNAs across several...
  2. ...show a good overall agreement, many subpaths are contributed solely by RNA-seq in platypus, cow, and zebrafish (Fig. 2B).View larger version: In this window In a new window Figure 2. Conservation and tissue regulation of a set of documented AS events. (A) Each event is designated by the name...
  3. ...et al. 2022). It is well established that tissue-specific miRNA expression patterns are conserved across evolution; therefore, we hypothesized that our historical miRNA profiles should cluster according to tissues rather than to their species identity. Only shared miRNAs among the four species...
  4. ...to that of certain vertebrate populations of miRNAs ( Tanzer and Stadler 2006 ). View larger version: In this window In a new window Figure 1. snoRNA representation in the of platypus. ( A ) snoRNAs with corresponding paralogs distributed by cis - or trans -duplication (trans). (Red lettering) snoRNAs conserved...
  5. ..., comparative mapping shows that, contrary to earlier reports, there is no homology between the platypus and therian X chromosomes. Orthologs of genes in the conserved region of the human X (including SOX3 , the gene from which SRY evolved) all map to platypus chromosome 6, which therefore represents...
  6. ...through a bite, as do snakes and shrews, male platypuses have venomous spurs on each hind leg. The platypus genome sequence provides a unique opportunity to unravel the evolutionary history of many of these interesting features. While searching the platypus genome for the sequences of antimicrobial...
  7. ...conserved) (Simakov et al. 2013; Li et al. 2022).We used KaKs_Calculator (v2.0) (Zhang 2022) to calculate the Ka/Ks ratios of paralogous gene pairs between macrochromosomes and microchromosomes, and gene expression values for L. osseus RNA-seq data were calculated using featureCounts (v2.0.2) (Liao et al...
  8. ...the APGs. MHC-I genes exhibit lineage-specific duplications and signs of concerted evolution, resulting in poorly resolved phylogenies. In contrast, MHC-II genes are more conserved and exhibit extensive trans-species polymorphism. Expression and polymorphism patterns identify putative nonclassical MHC...
  9. ...diversity of vertebrate chromatin conformation, here we generate de novo assemblies for two cryptodiran (hidden-neck) turtles via Illumina sequencing, chromosome conformation capture, and RNA-seq: Apalone spinifera (ZZ/ZW, 2n = 66) and Staurotypus triporcatus (XX/XY, 2n = 54). We detected differences...
  10. ...-13 and lin-39 orthologs, HOXA1 and HOXA5, respectively. Scans of the HOXA clusters in dog, opossum, platypus, and frog also revealed this pairing ( Fig. 6A ). Among the vertebrates alone, sequence conservation was high, indicating that these hits were located in functionally important DNA ( Fig. 6B...
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