[1] 陈辉. 猪重要经济性状选择的遗传进展[J].猪业科学, 2019, 36(1):116-118. [2] 刘航,侯黎明,王彬彬,等.显性效应对苏淮猪肉色性状遗传评估和基因组选择的影响[J].畜牧与兽医, 2021, 53(6):1-6. [3] 廖印长, 张跃博, 何俊.猪肉质性状全基因组关联分析的研究进展[J].畜牧与兽医, 2022, 54(8):125-131. [4] 陈艳珍. 猪肉品质的评定及影响因素[J].中国畜牧兽医, 2012, 39(7):155-158. [5] VAFAEE-SHAHI M,FARHADI M,RAZMARA E,et al.Novel phenotype and genotype spectrum of NARS2 and literature review of previous mutations[J]. Irish journal of medical science,2022,191(4):1877-1890. [6] ZHANG Y, ZHAO X, XU Y, et al.Study of novel NARS2 variants in patient of combined oxidative phosphorylation deficiency 24[J]. Translational pediatrics, 2022, 11: 448-457. [7] AL-SHARIF F, ALSADEQ H, ROZAN A, et al.Bilateral nonsyndromic sensorineural hearing loss caused by a NARS2 mutation[J]. Cureus, 2022, 14(11): e31467. [8] TANAKA R, TAKEGUCHI R, KURODA M, et al.Novel NARS2 variant causing leigh syndrome with normal lactate levels[J]. Human genome variation, 2022, 9(1):12. [9] WEI N, ZHAGN Q, YANG X L.Neurodegenerative charcot-marie-tooth disease as a case study to decipher novel functions of aminoacyl-tRNA synthetases[J]. Journal of biological chemistry, 2019, 294(14):5321-5339. [10] LANDRIEU I, VANDENBOL M, HARTLEIN M, et al.Mitochondrial asparaginyl-tRNA synthetase is encoded by the yeast nuclear gene YCR24c[J]. European journal of biochemistry, 1997, 243: 268-273. [11] HU W, FANG H, PENG Y, et al.Clinical and genetic analyses of premature mitochondrial encephalopathy with epilepsia partialis continua caused by novel biallelic NARS2 mutations[J]. Frontiers in neuroscience, 2022, 16:1076183. [12] SIMON M, RICHARD E M, WANG X, et al.Mutations of human NARS2, encoding the mitochondrial asparaginyl-tRNA synthetase, cause nonsyndromic deafness and leigh syndrome[J]. PLoS genetics, 2015, 11(3): e1005097. [13] SOFOU K, KOLLBERG G, HOLMSTROM M, et al.Whole exome sequencing reveals mutations in NARS2 and PARS2, encoding the mitochondrial asparaginyl-tRNA synthetase and prolyl-tRNA synthetase, in patients with alpers syndrome[J]. Molecular genetics & genomic medicine, 2015, 3:59-68. [14] MIZUGUCHI T,NAKASHIMA M,KATO M,et al.PARS2 and NARS2 mutations in infantile-onset neurodegenerative disorder[J]. Journal of human genetics, 2017, 62:525-529. [15] 曹艳娟. 不同表达水平基因内含子与mRNA序列的匹配特征[D].呼和浩特:内蒙古农业大学, 2023. [16] OLSON S, BLANCHETTE M, PARK J, et al.A regulator of dscam mutually exclusive splicing fidelity[J]. Nature structural & molecular biology, 2007, 14(12): 1134-1140. [17] WANG Z, BURGE C B.Splicing regulation: From a parts list of regulatory elements to an integrated splicing code[J]. RNA, 2008, 14(5): 802-813. [18] 张钏. 甘肃地区遗传代谢病的遗传图谱及PAH基因深部内含子变异致病性研究[D].北京:北京协和医学院, 2022. [19] SCIARRILLO R, WOJTUSZKIEWICZ A, ASSARAF Y G, et al.The role of alternative splicing in cancer: From oncogenesis to drug resistance[J]. Drug resistance updates, 2020, 53: 100728. [20] PADGETT R A.New connections between splicing and human disease[J]. Trends in genetics, 2012, 28(4): 147-154. [21] 刘玉, 张林林, 房义,等.湖羊STAT5a基因第10内含子多态性及其与泌乳性状的关联分析[J].中国畜牧兽医, 2023, 50(9):3680-3687. [22] 张方玮, 张琪, 张云鹏,等.松辽黑猪KPNA7基因多态性及其与繁殖性状的关联分析[J].中国畜牧杂志, 2023, 59(9): 235-239. |