Abstract:As a step toward the goal of adding the cattle genome to those available for multispecies comparative genome analysis, 40,224 cattle BAC clones were end-sequenced, yielding 60,547 sequences (BAC end sequences, BESs) after trimming with an average read length of 515 bp. Cattle BACs were anchored to the human and mouse genome sequences by BLASTN search, revealing 29.4% and 10.1% significant hits (E < e-5), respectively. More than 60% of all cattle BES hits in both the human and mouse genomes are located… Show more
“…It results in the lower bound bound(e) = 4 [37] that also gives a good approximation for br(e). On the other hand, one can estimate br(e 1 , e 2 ) as the number bound(e 1 , e 2 ) of vertices shared between non-trivial cycles in the breakpoint graphs corresponding to the branches e 1 and e 2 (similar approach was used in [22] and later explored in [25,31]). Assuming that the genomes at the internal nodes of the phylogenetic tree can be reliably reconstructed [4,25,26,45], one can compute bound(e) and bound(e 1 , e 2 ) for all (pairs of) branches.…”
An important question in genome evolution is whether there exist fragile
regions (rearrangement hotspots) where chromosomal rearrangements are happening
over and over again. Although nearly all recent studies supported the existence
of fragile regions in mammalian genomes, the most comprehensive phylogenomic
study of mammals (Ma et al. (2006) Genome Research 16, 1557-1565) raised some
doubts about their existence. We demonstrate that fragile regions are subject
to a "birth and death" process, implying that fragility has limited
evolutionary lifespan. This finding implies that fragile regions migrate to
different locations in different mammals, explaining why there exist only a few
chromosomal breakpoints shared between different lineages. The birth and death
of fragile regions phenomenon reinforces the hypothesis that rearrangements are
promoted by matching segmental duplications and suggests putative locations of
the currently active fragile regions in the human genome
“…It results in the lower bound bound(e) = 4 [37] that also gives a good approximation for br(e). On the other hand, one can estimate br(e 1 , e 2 ) as the number bound(e 1 , e 2 ) of vertices shared between non-trivial cycles in the breakpoint graphs corresponding to the branches e 1 and e 2 (similar approach was used in [22] and later explored in [25,31]). Assuming that the genomes at the internal nodes of the phylogenetic tree can be reliably reconstructed [4,25,26,45], one can compute bound(e) and bound(e 1 , e 2 ) for all (pairs of) branches.…”
An important question in genome evolution is whether there exist fragile
regions (rearrangement hotspots) where chromosomal rearrangements are happening
over and over again. Although nearly all recent studies supported the existence
of fragile regions in mammalian genomes, the most comprehensive phylogenomic
study of mammals (Ma et al. (2006) Genome Research 16, 1557-1565) raised some
doubts about their existence. We demonstrate that fragile regions are subject
to a "birth and death" process, implying that fragility has limited
evolutionary lifespan. This finding implies that fragile regions migrate to
different locations in different mammals, explaining why there exist only a few
chromosomal breakpoints shared between different lineages. The birth and death
of fragile regions phenomenon reinforces the hypothesis that rearrangements are
promoted by matching segmental duplications and suggests putative locations of
the currently active fragile regions in the human genome
“…Gene indices have also been constructed or are under construction for various species (14,102,105,113,114,115). Comparative maps were developed concurrently with genetic maps and are continuously being refined to link farm animal genome information with the more advanced structural and functional genomic data of other species, such as humans and mice (14,16,18,29,64,73,78,105). Recently developed comparative mapping tools (47,64,78)…”
The first genome sequence assemblies of farm animal species are now accessible through public domain databases, and further sequencing projects are in rapid progress. In addition, large collections of expressed sequences have been obtained, which will aid in constructing annotated transcript maps for many economically important species. Thus, the breeding of farm animals is entering the post-genome era. Functional genomics, defined as applying global experimental approaches to assess gene function, by using the information and reagents provided by structural genomics (i.e. mapping and sequencing), has become the focus of interest. Combining a holistic view of phenotypes at the molecular level with genetic marker data seems a particularly promising approach for improving health and welfare traits in farm animals. These traits are often difficult to define. They suffer from low heritabilities and a corresponding lack of genetic gain in conventional selection and breeding programmes. At the same time, genomic information from micro-organisms and parasites offers the potential for new vaccines and therapeutics. This review describes major functional genomics tools, lists genomic resources available for farm animals and discusses the prospects and challenges of functional genomics in improving the health and welfare of farm animals.
“…The locations of microsatellites were analyzed using a new version of COMPASS software (with the kind help of Dr. Harris A. Lewin, University of Illinois at Urbana-Champaing, IL, USA) to predict the position of each microsatellite on Hanwoo chromosomes (Larkin et al, 2003).…”
Section: Pcr Primer Design and Chromosome Localizationmentioning
To isolate the microsatellites from the chromosomal DNA of the Korean cattle (Hanwoo) and to use those for the genetic selection, four bacteriophage genomic libraries containing the chromosomal DNA of six Hanwoo steers showing the differences in meat quality and quantity were used. Screening of the genomic libraries using 32 P-radiolabeled 5`-(CA) 12 -3' nucleotide as a probe, resulted in isolation of about 3,000 positive candidate bacteriophage clones that contain (CA) n -type dinucleotide microsatellites. After confirming the presence of microsatellite in each positive candidate clone by Southern blot analysis, the DNA fragments that include microsatellite and flanking sequences possessing less than 2 kb in size, were subcloned into plasmid vector. Results from the analysis of microsatellite length polymorphism, using twenty-two PCR primers designed from flanking region of each microsatellite DNA, demonstrated that 208 and 210 alleles of HW-YU-MS#3 were closely related to the economic traits such as marbling score, daily gain, backfat thickness and M. longissimus dorsi area in Hanwoo. Interestingly, HW-YU-MS#3 microsatellite was localized in bovine chromosome 17 on which QTLs related to regulation of the body fat content and muscle hypertrophy locus are previously known to exist. Taken together, the results from the present study suggest the possible use of the two alleles as a DNA marker related to economic trait to select the Hanwoo in the future.
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