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Sex chromosome-to-autosome transposition events counter Y-chromosome gene loss in mammals

TLDR
Findings indicate that Y-linked gene loss emerges as an additional driver of gene transposition from the sex chromosomes, a phenomenon thought to be driven primarily by meiotic sex chromosome inactivation, and is widespread among mammalian species.
Abstract
Although the mammalian X and Y chromosomes evolved from a single pair of autosomes, they are highly differentiated: the Y chromosome is dramatically smaller than the X and has lost most of its genes. The surviving genes are a specialized set with extraordinary evolutionary longevity. Most mammalian lineages have experienced delayed, or relatively recent, loss of at least one conserved Y-linked gene. An extreme example of this phenomenon is in the Japanese spiny rat, where the Y chromosome has disappeared altogether. In this species, many Y-linked genes were rescued by transposition to new genomic locations, but until our work presented here, this has been considered an isolated case. We describe eight cases of genes that have relocated to autosomes in mammalian lineages where the corresponding Y-linked gene has been lost. These gene transpositions originated from either the X or Y chromosomes, and are observed in diverse mammalian lineages: occurring at least once in marsupials, apes, and cattle, and at least twice in rodents and marmoset. For two genes - EIF1AX/Y and RPS4X/Y - transposition to autosomes occurred independently in three distinct lineages. Rescue of Y-linked gene loss through transposition to autosomes has previously been reported for a single isolated rodent species. However, our findings indicate that this compensatory mechanism is widespread among mammalian species. Thus, Y-linked gene loss emerges as an additional driver of gene transposition from the sex chromosomes, a phenomenon thought to be driven primarily by meiotic sex chromosome inactivation.

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Mammalian Y chromosomes retain widely expressed dosage-sensitive regulators

TL;DR: This article reconstructed the evolution of the Y chromosome across eight mammals to identify biases in gene content and the selective pressures that preserved the surviving ancestral genes, and concluded that the gene content of Y chromosome became specialized through selection to maintain the ancestral dosage of homologous X-Y gene pairs that function as broadly expressed regulators of transcription, translation and protein stability.
Journal ArticleDOI

Engineering resistance against Tomato yellow leaf curl virus via the CRISPR/Cas9 system in tomato

TL;DR: The results confirmed the efficiency of the CRISPR/Cas9 system for stable engineering of TYLCV resistance in N. benthamiana and tomato, and opens the possibilities of engineering virus resistance against single and multiple infectious viruses in other crops.
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Sex Chromosome Evolution: So Many Exceptions to the Rules.

TL;DR: How the diversity in sex chromosomes across taxa highlights an equal diversity in each stage of sex chromosome evolution is concentrated on.
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Dosage compensation of the sex chromosomes and autosomes.

TL;DR: This review will consider the evidence for dosage compensation and the molecular mechanisms implicated, and several modes of dosage compensation have evolved.
References
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Journal ArticleDOI

MUSCLE: multiple sequence alignment with high accuracy and high throughput

TL;DR: MUSCLE is a new computer program for creating multiple alignments of protein sequences that includes fast distance estimation using kmer counting, progressive alignment using a new profile function the authors call the log-expectation score, and refinement using tree-dependent restricted partitioning.
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Ultrafast and memory-efficient alignment of short DNA sequences to the human genome

TL;DR: Bowtie extends previous Burrows-Wheeler techniques with a novel quality-aware backtracking algorithm that permits mismatches and can be used simultaneously to achieve even greater alignment speeds.
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PAL2NAL: robust conversion of protein sequence alignments into the corresponding codon alignments

TL;DR: PAL2NAL is a web server that constructs a multiple codon alignment from the corresponding aligned protein sequences that can be used to evaluate the type and rate of nucleotide substitutions in coding DNA for a wide range of evolutionary analyses.
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TimeTree: a public knowledge-base of divergence times among organisms

TL;DR: TimeTree brings time estimates from molecular data together in a consistent format and uses a hierarchical structure, corresponding to the tree of life, to maximize their utility.
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