| dc.description.abstract | The objectives of this research were to identify polymorphism of calpastatin gene and to investigate any association of calpastatin genotype on body weight of local sheeps. A total number of DNA samples were collected from 288 heads of local
sheeps from 8 populations. Two local sheep samples were medium tail sheeps (MTSs) of a Garut fighting type from Ciomas/Bogor (29) and a Garut meat type from Margawati (29). The remaining six local sheep population were one thin tail
sheep (TTS) from Jonggol (36); and five fat tail (FTSs) from Indramayu (43), Madura (43), Sumbawa (26), Rote (36) and Donggala (46) respectively. Genomic DNAs of those blood of local sheeps were extracted by a standard phenol-chloroform
protocol and amplified using a polymerase chain reaction (PCR) technique. PCR reaction was carried out in a thermocycler (Takara PCR of Thermal Cycler MP4) and PCR products were digested with Msp 1 enzyme restriction using a Restriction
Fragment Length Polymorphism (RFLP) technique. The PCR-RFLP products were separated at 8% polyacrylamide gel electrophoresis (PAGE). A silver-staining method then was applied to detect fragments. Genetic variations between local sheep populations were calculated based on frequencies of genotypes and alelles. The association between genotype of calpastatin gene and body weight of local sheeps were calculated by General Linear Model method by SAS version 6.12. A length of 622 base pairs (bp) of the calpastatin gene of the Indonesian local sheeps was successfully amplified by the PCR technique. An MspI restriction enzyme cut the PCR product into two different length fragments, those were 336 bp and 286 bp designated as M allele of the CAST-Msp1; whilst that unsuccessfully cut PCR product resulted one fragment 622 bp designated as N allele of the CAST-Msp1. Locus of the CAST-Msp1 gene in most local sheeps studied was polymorphic, the exception was in the FTS from Rote of which monomorphic. The highest frequency of the M allele was in the fighting Garut sheep from Ciomas (0.29), whilst
the lowest was in the FTS from Rote (0.00). However, frequencies of the M allele of FTSs from Sumbawa and Madura were similar (0.04). Further, frequencies of the M allele of local sheeps from Margawati, Jonggol, Indramayu, and Donggala were
0.24, 0.16, 0.13 and 0.12 respectively. The highest frequency of MN genotype was observed in the Garut fighting sheep from Ciomas (0.58), but the lowest was in the FTS from Rote (0.00). The heterosigosity was observed differently among populations. The highest heterosigosity was also identified in the Garut fighting sheep in Ciomas (0.43), while FTSs of both of Sumbawa and Madura were for the lowest (0.08). Results of this study showed that there was a definit association betwen calpastatin genotype and body weight of male sheeps from which the MN genotype significantly related to a higher body weight compared to that of
the NN genotype. | id |
| dc.description.abstract | Penelitian ini bertujuan mengidentifikasi polimorfisme dari gen calpastatin (lokus CAST-Msp1) dan memeriksa hubungan antara genotipe calpastatin dari lokus CAST-Msp1 dengan bobot hidup pada domba lokal. Jumlah sampel DNA dikoleksi pada 288 ekor domba lokal dari 8 populasi. Dua sampel adalah Domba Ekor Sedang (DES) tipe tangkas Garut dari Ciomas/Bogor (29), dan tipe pedaging Garut dari Margawati (29). Enam sampel lainnya adalah Domba Ekor Tipis (DET) dari Jonggol (36); serta Domba Ekor Gemuk (DEG) dari Indramayu (43), Madura (43), Donggala (46), Sumbawa (26), dan Rote (36). Genom DNA diekstrak menggunakan phenol-chloroform protocol kemudian diamplifikasi dengan teknik polymerase chain reaction (PCR). Produk PCR dipotong menggunakan enzim Msp1 dengan teknik Restriction Fragment Length Polymorphism (RFLP). Produk PCR-RFLP selanjutnya dipisahkan menggunakan polyacrylamide gel electrophoresis (PAGE). 8% Metoda pewarnaan perak dipakai dalam mendeteksi adanya fragmen. Keragaman genetik antara populasi domba lokal dihitung berdasarkan frekuensi genotipe dan alel. Pengaruh genotipe calpastatin terhadap bobot hidup ternak dianalisis menggunakan prosedur General Linear Model SAS versi 6.12. Satu pita 622 pb (pasangan basa) dari gen calpastatin berhasil diamplifikasi pada domba
lokal Indonesia menggunakan teknik PCR. Enzim Msp1 memotong produk PCR menjadi dua fragmen, yakni 336 pb dan 286 pb, yang dinyatakan sebagai alel M dari gen calpastatin lokus CAST-Msp1; sebaliknya produk PCR yang tidak terpotong menghasilkan 622 pb, yang dinyatakan sebagai alel N. Hampir semua domba lokal pengamatan bersifat polimorfik untuk gen calpastatin lokus CAST-Msp1, kekecualian untuk DEG dari Rote yang bersifat monomorfik. Frekuensi tertinggi dari alel M
ditemukan pada domba adu tangkas Garut dari Ciomas (0,29), sebaliknya frekuensi terendah pada DEG dari Rote (0,00), dan frekuensi alel M di Sumbawa dan Madura adalah sama (0,04). Frekuensi alel M domba lokal dari Margawati, Jonggol,
Indramayu, dan Donggala berurutan 0,24, 0,16, 0,13 dan 0,12. Identifikasi polimorfisme gen calpastatin dengan teknik RFLP dengan demikian menghasilkan dua genotipe yaitu MN dan NN. Frekuensi tertinggi dari genotipe MN teramati pada domba tangkas Garut di Ciomas (0,58), sebaliknya terendah pada DEG di Rote (0,00). Heterosigositas tinggi teridentifikasi antara populasi. Frekuensi heterosigositas tertinggi ditemukan pada domba tangkas Garut di Ciomas (0,43); sebaliknya DEG di Sumbawa dan Garut mempunyai frekuensi heterosigositas terendah (0,08). Hasil menunjukkan bahwa domba jantan bergenotipe MN mempunyai bobot hidup lebih tinggi (P<0,05) bila dibandingkan dengan domba bergenotipe NN | id |
