Molecular genetic variation in the Galway sheep breed

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Molecular genetic variation in the Galway sheep breed Dawn J. Howard Ph.D. 1,2 1 Teagasc, Athenry, Galway. 2 Animal Genomics Laboratory, UCD.

Context Worldwide 1,000 breeds have become extinct during the last 100 years (FAO) Extinct Irish breeds include; Irish Hobby horse White-tailed eagle Kerry Mountain and Cladagh sheep (lost in 1970s) Endangered Irish breeds include: Kerry, Dexter and Irish moiled cattle Connemara pony and Irish Draught horse Galway sheep breed

Galway Breed The Galway breed is the only native Irish sheep breed. It is listed by FAO (DADIS) as a breed in danger of extinction Due to decrease in numbers in 1980s and 1990s

Historical Background A long-woolled sheep breed being developed in Ireland up to mid 1800s Breeds used in its development include; New Leicester Southdown Cotswold Merino sheep Connaught was the principal breeding area At first the breed known as Roscommon breed 1870 recognised by Royal Dublin Society (RDS) 1895 Roscommon Breeders Society was formed

Historical Background contd. By mid 1920s Roscommon Breeders Society became defunct 1923 the Galway Sheep Breeders Society was formed For a period the RDS listed both the Galway and Roscommon breeds From 1937 the Roscommon breed no longer listed in RDS catalogues Galway breed was the predominant breed until the mid 1970s when Suffolk cross lambs became more popular

No. ewes No. flocks 1200 1000 800 600 400 200 0 Number of pedigree Galway ewes and flocks 1975 1980 1985 1990 1995 2000 Year No. Ewes No. Flocks 40 35 30 25 20 15 10 5 0

Population in 1994 9 flocks 169 ewes 11 rams of which 9 came from 8 core breeders

Numberof animals Population history of Galway breed 1000 900 800 Breeding females Breeding males Total census population Effective population size Ne 700 600 500 400 300 200 100 0 1994 1995 1996 1997 1998 1999 2000 2001 2002 2003 2004 2005 2006 2007 2008 Year

Overall Objectives Objective 1: Establish a DNA bank for pedigree Galway population. Objective 2: Establish the level of genetic variation in the Galway breed, and compare this to other populations that have not experienced a bottleneck

Methodology 1: Methodology The DNA bank collection of blood, extraction of DNA, long-term storage Methodology 2: The genetic variation was evaluated from three perspectives: 1. 16 microsatellite loci markers 2. Control region of mitochondrial genome 3. Genetic markers on Y chromosome

Background for microsatellite variation study Microsatellites are repetitive stretches of DNA, usually di-, tri- or tetra-nucleotide repeats Microsatellite loci generally have many alleles and are considered to be neutral with respect to fitness

Selection of microsatellite Considerations: markers for study Good coverage across the sheep genome Selected microsatellites that had been used in other studies Econogene project and on FAO list Achievable workload 16 markers chosen

Chromosomal location of microsatellite markers OarFCB128 OarFCB11 BM1824 MAF64 1 2 3 OarCP34 OarCP43 OarHH35 OarAE129 4 5 6 7 8 BM1329 OarFCB193 BM757 INRA63 9 10 11 12 13 MAF65 14 15 16 17 18 OarFCB304 19 20 21 22 23 OarVH72 24 25 26 X X TGLA54

Selection of animals for study Total of 94 Galways chosen from bank All sires represented as equally as possible Only one offspring per dam 70 Suffolk & 58 Texel Both large populations and no known bottleneck provide direct comparison of the Galway with non-endangered Irish populations.

Methods EXTRACTION microsatellite PCR Sheep blood sample Sheep DNA Fluorescently labelled microsatellite DNA Output = microsatellite allele length in base pairs ABI 3100 Genetic Analyser 96 well microtitre plate

ABI 3100 genetic analyser output Heterozygous individual Homozygous individual 170bp 121bp 172bp

Genetic variation results Mean Diversity measure Galway Suffolk Texel No. of alleles 4.81 3.50 4.44 Effective no. of alleles 3.31 2.53 3.02 Allelic richness 4.91 3.92 4.33 Observed heterozygosity 0.60 0.60 0.52 Expected heterozygosity 0.69 0.59 0.58 PIC 0.62 0.51 0.60

Analysis of genetic differentiation Genetic structure - Sewell Wrights F- statistics Measures deviations of genotype frequencies in subdivided populations in terms of F IS, F IT, F ST High differentiation observed among the three Irish breeds (F ST = 0.15) Galway, Suffolk and Texel - heterozygote deficiency

Phylogenetic analysis Neighbour-joining tree constructed from allele sharing matrix data for three Irish breeds plus 57 populations from Econogene project Grouped Galway and Suffolk closer together than either is to Texel

Mitochondrial variation study Maternally inherited No recombination High mutation rate Genome is 16 kb with 1.2 kb hypervariable D-loop. Mitochondrial DNA used to investigate: Maternal lineages Genetic variation

Material used for study Total of 30 Galway sheep chosen from the DNA bank. DNA from 12 Suffolk and 10 Texel animals Selected 188 sheep mitochondrial DNA sequences from GenBank.

D-loop Methods Electrophoresis λhind III 1 2 3 4 λhind III 100bp Sheep mtdna PCR Thermocycler 1.2kb Neg ABI 3700 sequencer electropherogram

Phylogenetic analysis Galway HG B HG D Suffolk Unknown HG HG C Texel HG A Unknown HG

Haplogroup B Haplogroup A Haplogroup C Haplogroup D Karachas Karachas Karachas Karachas Mongolian Mongolian Mongolian Mongolian Karachul Karachul Karachul Small Tailed Han Small Tailed Han Small Tailed Han Churra Algarvia Churra Algarvia Churra Algarvia Tushin Tushin Tushin Hu Hu Hu Karachai Karachai Karachai Texel Finnsheep Speal Sheep Olkusz Polled Dorset Garole Saloia Badana Tibetan Galway Suffolk Oxford Down Romanov Swiniarka Russian Tsigai Merionpreto Old Speal Sheep Texel Finnsheep Speal sheep Olkusz Polled Dorset Garole Saloia Badana Tibetan Total no. breeds = 25 Total no. breeds = 15 Total no. breeds = 9 Total no. breeds = 3 Total no. sequences = 179 Total no. sequences = 36 Total no. sequences = 18 Total no. sequences = 3

Mitochondrial DNA variation Global and Irish mtdna sequences Nucleotide diversity (π) of 4 haplogroups (HG) HG B most diverse Greatest divergence (k) between HG A and C π for three Irish breeds Texel most diverse Greatest divergence (k) was observed when Texel was compared with either of the other two breeds

Background for Y chromosome study Pseudoautosomal region - recombines with X Male Specific Y (MSY) region - no recombination. MSY genes are paternally inherited. & ZFY Two known genes in sheep MSY region, ZFY & SRY Human

Methods ZFY intron DNA from males 950bp 850bp PCR 500bp Lane 1: 100bp ladder, Lane 2: Empty, Lane 2 7: samples, Lane 8: Neg control SRY SNP Lane 1: 100bp ladder, Lane 6: 100bp ladder, Lane 2 5: samples SRY microsatellite ABI 3700 sequencer Y chromosome ~140bp Lane 1: λ Hind III, Lane 2: 100bp ladder, Lane 3 12: samples Lane 13: Neg control

Methods 10 Galway males, 11 Suffolk males, 9 Texel males. Haplotypes were based on: Single nucleotide polymorphism (SNP) called oy1 in SRY promoter region SRY microsatellite called SRYM18 Analysis of ZFY intron diversity

Results There was no variation in the ZFY intron SRY SNP + SRY microsatellite = haplotype H5 in Irish breeds Haplotype [TTTTG] m Indel G/- [TG] n SRY SNP Breed H5 3 G 16 G Galway H5 3 G 16 G Suffolk H5 3 G 16 G Texel H5 is present in sheep from Asia and Europe, absent from African sheep

Conclusions from microsatellites The genetic variation in the Galway breed is within the range reported for other breeds. No evidence that the Galway breed has lost genetic diversity. So bottleneck in 1994 did not have any major consequences Galway phylogenetically closer to the Suffolk than to Texel

Conclusions from mtdna Galway and Suffolk have one maternal lineage HG B Texel has two maternal lineages HG B and A Greatest divergence between HG A and C The divergence was least between Galway and Suffolk Of the three Irish breeds Texel most diverse

Conclusions from Y chromosome One paternal haplotype identified in the Galway, Suffolk and Texel breeds There was no variation in ZFY intron

Overall conclusion Current number of pedigree Galway sheep (800 ewes in 50 registered flocks) is sufficient to maintain the existing genetic diversity.

Acknowledgements Dr. J.P. Hanrahan, Teagasc, Athenry, Galway. Prof. David E. MacHugh, Animal Genomics Laboratory, UCD. Dr. Stephen Park, Animal Genomics Laboratory, UCD. Dr. Susanna Barth, Teagasc, Oakpark, Carlow

Thank you