Capturing benefits from the bovine genome sequence
Ross L. TellamCSIRO Livestock Industries, Queensland Biosciences Precinct, 306 Carmody Road, St Lucia, Qld 4067, Australia. Email: Ross.Tellam@csiro.au
Australian Journal of Experimental Agriculture 47(9) 1039-1050 https://doi.org/10.1071/EA06032
Submitted: 10 January 2006 Accepted: 6 September 2006 Published: 6 August 2007
Abstract
The bovine genome sequence in ‘draft’ form will be complete in 2007. The availability of the sequence and very large numbers of single nucleotide polymorphisms will have profound effects on livestock production. The dairy industry is well positioned to capture the benefits of this enormous and enabling resource because of its comprehensive databases containing phenotypic and pedigree data for large numbers of animals, intense utilisation of genetics in breeding programs and efficient management of reproductive performance. The bovine genome sequence will assist in the development of novel products, especially value-added products, and markedly enhance the rate of genetic gain in the Australian dairy population. The immediate challenge facing the industry is the integration of new technological capabilities into existing breeding programs and production systems.
Additional keywords: cow, ruminant.
Acknowledgements
I thank a long list of colleagues, particularly members of the BGSP and its advisory groups for stimulating thought and their enormous breadth of knowledge.
Austin CP,
Battey JF,
Bradley A,
Bucan M, Capecchi M , et al.
(2004) The knockout mouse project. Nature Genetics 36, 921–924.
| Crossref | GoogleScholarGoogle Scholar | PubMed |
[Verified 25 May 2007]
Clop A,
Marcq F,
Takeda H,
Pirottin D, Tordoir X , et al.
(2006) A mutation creating a potential illegitimate microRNA target site in the myostatin gene affects muscularity in sheep. Nature Genetics 38, 813–818.
| Crossref | GoogleScholarGoogle Scholar | PubMed |
[Verified 25 May 2007]
Pastinen T,
Sladek R,
Gurd S,
Sammak A, Ge B , et al.
(2004) A survey of genetic and epigenetic variation affecting human gene expression. Physiological Genomics 16, 184–193.
| Crossref | GoogleScholarGoogle Scholar | PubMed |
[Verified 25 May 2007]
Vuocolo T,
Cockett N, Tellam RL
(2005) Expression of imprinted genes surrounding the callipyge mutation in ovine skeletal muscle. Australian Journal of Experimental Agriculture 45, 879–892.
| Crossref | GoogleScholarGoogle Scholar |
Wall RJ,
Powell AM,
Paape MJ,
Kerr DE,
Bannerman DD,
Pursel VG,
Wells KD,
Talbot N, Hawk HW
(2005) Genetically enhanced cows resist intramammary Staphylococcus aureus infection. Nature Biotechnology 23, 445–451.
| Crossref | GoogleScholarGoogle Scholar | PubMed |
Waterland RA, Garza C
(1999) Potential mechanisms of metabolic imprinting that lead to chronic disease. American Journal of Clinical Nutrition 69, 179–197.
| PubMed |
Weaver IC,
Cervoni N,
Champagne FA,
D’Alessio AC,
Sharma S,
Seckl JR,
Dymov S,
Szyf M, Meaney MJ
(2004) Epigenetic programming by maternal behavior. Nature Neuroscience 7, 847–854.
| Crossref | GoogleScholarGoogle Scholar | PubMed |
Whitelaw E, Martin DI
(2001) Retrotransposons as epigenetic mediators of phenotypic variation in mammals. Nature Genetics 27, 361–365.
| Crossref | GoogleScholarGoogle Scholar | PubMed |
Williams JL,
Eggen A,
Ferretti L,
Farr CJ, Gautier M , et al.
(2002) A bovine whole-genome radiation hybrid panel and outline map. Mammalian Genome 13, 469–474.
| Crossref | GoogleScholarGoogle Scholar | PubMed |
Wilson HL,
Aich P,
Roche FM,
Jalal S,
Hodgson PD,
Brinkman FS,
Potter A,
Babiuk LA, Griebel PJ
(2005) Molecular analyses of disease pathogenesis: application of bovine microarrays. Veterinary Immunology and Immunopathology 105, 277–287.
| Crossref | GoogleScholarGoogle Scholar | PubMed |
Womack JE
(2005) Advances in livestock genomics: opening the barn door. Genome Research 15, 1699–1705.
| Crossref | GoogleScholarGoogle Scholar | PubMed |
1 ‘Finished’ sequence is defined as ‘the clone insert is contiguously sequenced with high quality standard error rate of 0.01% – there are usually no gaps in the sequence’. A ‘draft’ sequence can have different definitions depending on the specific project but a typical definition is: ‘at least 3–4× of the estimated clone insert is covered in Phred Q20 bases in the whole genome shotgun stage. Clone sequence may contain several pieces of sequence, separated by gaps. The true order and orientation of these pieces may not be known.’ (National Centre for Biotechnology Information, Bethesda, MD).