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. 2022 Mar 9;12(6):686. doi: 10.3390/ani12060686

Table 5.

The effects of genotype of the capn1_184 SNP on the tenderness phenotype, myofibril fragment length (MFL) of representative purebred South African beef bulls during three to 20 days of ageing and on the muscle protease enzyme system during the first 20 h post-mortem.

capn1_184 *GG (n = 77) AG (n = 66) AA (n = 23) p-Value
(Simplified)
Genotype
Effect
MFL (d 3) 33.47 ± 0.65 35.48 ± 0.72 41.57 ± 1.74 0.1810
MFL (d 9) 24.67 ± 0.42 c 26.20 ± 0.47 b 31.98 ± 1.12 a 0.0242 −22.9%
MFL (d 14) 22.50 ± 0.38 y 24.05 ± 0.42 y 30.54 ± 1.02 z 0.0771 −26.3%
MFL (d 20) 20.92 ± 0.31 21.54 ± 0.35 25.70 ± 0.84 0.1557
calpastatin (1 h) 1.99 ± 0.04 1.99 ± 0.04 2.23 ± 0.09 0.4096
calpastatin (20 h) 1.69 ± 0.04 1.64 ± 0.05 1.81 ± 0.11 0.6957
calpain-1 (1 h) 1.47 ± 0.03 1.41 ± 0.03 1.32 ± 0.08 0.2095
calpain-1 (20 h) 1.13 ± 0.03 1.05 ± 0.04 0.97 ± 0.09 0.7597
calpain-2 (1 h) 1.00 ± 0.01 1.00 ± 0.01 0.98 ± 0.03 0.7125
calpain-2 (20 h) 1.04 ± 0.01 1.02 ± 0.01 0.98 ± 0.04 0.5729

*GG—the genotype that favored tenderness; least squares means (LSM) ± standard errors (SE) that were significantly different within rows or ageing periods (p ≤ 0.05) were indicated with different ascending letter superscripts (a, b, c), and those that tended to be significantly different (p ≤ 0.10) with different descending letter superscripts (z, y). MFL—myofibril fragment length.