Tissue sampling methods and standards for vertebrate genomics
Wong, P.B.Y., E.O. Wiley, W.E. Johnson, O.A. Ryder, S.J. O'Brien, D. Haussler, K.-P. Koepfli, M.L. Houck, P. Perelman, G. Mastromonaco, A.C. Bentley, B. Venkatesh, Genome 10K Community of Scientists, Y.-p. Zhang, and R.W. Murphy. In press. Tissue sampling methods and standards for vertebrate genomics. GigaScence.
The recent rise in speed and efficiency of new sequencing technologies have facilitated high-throughput sequencing of... more The recent rise in speed and efficiency of new sequencing technologies have facilitated high-throughput sequencing of genomes, assembly and analyses, advancing ongoing efforts to analyze genetic sequences across major vertebrate groups. Standardized procedures in acquiring high quality DNA and RNA and establishing cell lines from target species will facilitate these initiatives. We provide a legal and methodological guide according to four standards of acquiring and storing tissue for the Genome 10K project and similar initiatives as follows: four-star (banked tissue/cell cultures, RNA from multiple types of tissue for transcriptomes, and sufficient flash-frozen tissue for 1mg of DNA, all from a single individual); three-star (RNA as above and frozen tissue for 1mg of DNA); two-star (frozen tissue for at least 700μg of DNA); and one-star (ethanol-preserved tissue for 700μg of DNA or less of mixed quality). At a minimum, all tissues collected for the Genome 10K and other genomic projects should consider each species’ natural history and follow institutional and legal requirements. Associated documentation should detail as much information as possible about provenance to ensure representative sampling and subsequent sequencing. Hopefully, the procedures outlined here will not only encourage success in the Genome 10K project but also inspire the adaptation of standards by other genomic projects, including those involving other biota.
Liu, Z., G.-H. Li, J.-F. Huang, R.W. Murphy, and P. Shi. 2012. Hearing aid for vertebrates via multiple episodic adaptive events on prestin genes
Liu, Z., G.-H. Li, J.-F. Huang, R.W. Murphy, and P. Shi. 2012. Hearing aid for vertebrates via multiple episodic adaptive events on prestin genes. Molecular Biology and Evolution. DOI: 10.1093/molbev/mss087
Auditory detection is essential for survival and reproduction of vertebrates, yet the genetic changes underlying the... more
Auditory detection is essential for survival and reproduction of vertebrates, yet the genetic changes underlying the evolution and diversity of hearing are poorly documented. Recent discoveries concerning the prestin gene, which is responsible for cochlear amplification by electromotility, provide an opportunity to redress this situation. We identify prestin genes from the genomes of 14 vertebrates, including three fishes, one amphibian, one lizard, one bird, and eight mammals. An evolutionary analysis of these sequences and 34 previously known prestin genes reveals for the first time that this hearing gene was under positive selection in the most recent common ancestor (MRCA) of tetrapods. This discovery might document the genetic basis of enhanced high sound sensibility in tetrapods. An investigation of the adaptive gain and evolution of electromotility, an important evolutionary innovation for the highest hearing ability of mammals, detects evidence for positive selections on the MRCA of mammals, therians, and placentals, respectively. It is suggested that electromotility determined by prestin might initially appear in the MRCA of mammals and its functional improvements might occur in the MRCA of therian and placental mammals. Our patch clamp experiments further support this hypothesis, revealing the functional divergence of voltage-dependent nonlinear capacitance (NLC) of prestin from platypus, opossum, and gerbil. Moreover, structure-based cdocking analyses detect positively selected amino acids in the MRCA of placental mammals that are key residues in sulfate anion transport. This study provides new insights into the adaptation and functional diversity of hearing sensitivity in
vertebrates by evolutionary and functional analysis of the hearing gene of prestin.
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Seen by:Bayesian estimation of substitution rates from ancient DNA sequences with low information content
by Sergios-Orestis Kolokotronis
Systematic Biology
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Seen by:The biology of intron gain and loss.
Intron density in eukaryote genomes varies by more than three orders of magnitude, so there must have been extensive... more Intron density in eukaryote genomes varies by more than three orders of magnitude, so there must have been extensive intron gain and/or intron loss during evolution. A favored and partial explanation for this range of intron densities has been that introns have accumulated stochastically in large eukaryote genomes during their evolution from an intron-poor ancestor. However, recent studies have shown that some eukaryotes lost many introns, whereas others accumulated and/or gained many introns. In this article, we discuss the growing evidence that these differences are subject to selection acting on introns depending on the biology of the organism and the gene involved.
Early evolution: prokaryotes, the new kids on the block.
An RNA world is widely accepted as a probable stage in the early evolution of life. Two implications are that proteins... more An RNA world is widely accepted as a probable stage in the early evolution of life. Two implications are that proteins have gradually replaced RNA as the main biological catalysts and that RNA has not taken on any major de novo catalytic function after the evolution of protein synthesis, that is, there is an essentially irreversible series of steps RNA --> RNP --> protein. This transition, as expected from a consideration of catalytic perfection, is essentially complete for reactions when the substrates are small molecules. Based on these principles we derive criteria for identifying RNAs in modern organisms that are relics from the RNA world and then examine the function and phylogenetic distribution of RNA for such remnants of the RNA world. This allows an estimate of the minimum complexity of the last ribo-organism-the stage just preceding the advent of genetically encoded protein synthesis. Despite the constraints placed on its size by a low fidelity of replication (the Eigen limit), we conclude that the genome of this organism reached a considerable level of complexity that included several RNA-processing steps. It would include a large protoribosome with many smaller RNAs involved in its assembly, pre-tRNAs and tRNA processing, an ability for recombination of RNA, some RNA editing, an ability to copy to the end of each RNA strand, and some transport functions. It is harder to recognize specific metabolic reactions that must have existed but synthetic and bio-energetic functions would be necessary. Overall, this requires that such an organism maintained a multiple copy, double-stranded linear RNA genome capable of recombination and splicing. The genome was most likely fragmented, allowing each "chromosome" to be replicated with minimum error, that is, within the Eigen limit. The model as developed serves as an outgroup to root the tree of life and is an alternative to using sequence data for inferring properties of the earliest cells.

