{"title":"重新测序瑞典红牛的酪蛋白基因,使牛奶具有不同的蛋白质特征和极强的凝乳酶凝固特性","authors":"","doi":"10.3168/jdsc.2023-0412","DOIUrl":null,"url":null,"abstract":"<div><p>Impaired rennet coagulation properties in milk could lead to prolonged processing times and production losses. Heritability for milk coagulation has previously been estimated to be 0.28 to 0.45, indicating that genetic selection can be used to manipulate this trait. The CN proteins are expressed by the genes <em>CSN1S1, CSN2, CSN1S2</em>, and <em>CSN3</em> and are located on bovine chromosome 6. To better understand the effect of genetic variation in the CN genes on milk coagulation, blood and milk samples from 30 Swedish Red Dairy Cattle (RDC) with divergent coagulation properties were investigated. DNA from the 30 cows was sequenced for the CN genes to determine the theoretical AA sequence and to look for genetic variation in the untranslated regions. The aim is to confirm the protein genetic variants previously reported, while searching for additional genetic variation in the CN genes of 30 RDC. We observed genetic variation in 116 SNPs in the known CN genes where 10% of the SNPs are exon variants and the remaining 90% are intron variants. A total of 2.5% of the SNPs are found in the 5′- or 3′-untranslated region (UTR) regions of the exons; 2% are synonymous variants and 6% are missense variants that concurred with the known protein variants for <em>CSN1S1, CSN2</em>, and <em>CSN3</em>. Furthermore, 6% of the SNPs are splice polypyrimidine tract intron variants. The 2 genetic variants in the 5′- and 3′-UTR in <em>CSN1S1</em> and <em>CSN3</em> are found with protein variants <em>CSN1S1C</em> and <em>CSN3B</em>. Because both UTR variants are associated with gain and loss of micro RNA and transcription factors, this could explain differences in expression of the genetic protein variants. Preliminary chi-squared analysis and comparison with previous GWAS studies showed potential connections between the identified SNPs and coagulation properties of milk. By advancing the knowledge of the connection between the DNA sequence and the functional properties of the CN proteins, we hope to learn more about the cheese coagulation properties of milk from RDC.</p></div>","PeriodicalId":94061,"journal":{"name":"JDS communications","volume":"5 4","pages":"Pages 299-304"},"PeriodicalIF":0.0000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2666910224000267/pdfft?md5=ff57d97b1008b3477a97c2e6185e3cd8&pid=1-s2.0-S2666910224000267-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Re-sequencing of the casein genes in Swedish Red cattle giving milk with diverse protein profiles and extreme rennet coagulation properties\",\"authors\":\"\",\"doi\":\"10.3168/jdsc.2023-0412\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Impaired rennet coagulation properties in milk could lead to prolonged processing times and production losses. Heritability for milk coagulation has previously been estimated to be 0.28 to 0.45, indicating that genetic selection can be used to manipulate this trait. The CN proteins are expressed by the genes <em>CSN1S1, CSN2, CSN1S2</em>, and <em>CSN3</em> and are located on bovine chromosome 6. To better understand the effect of genetic variation in the CN genes on milk coagulation, blood and milk samples from 30 Swedish Red Dairy Cattle (RDC) with divergent coagulation properties were investigated. DNA from the 30 cows was sequenced for the CN genes to determine the theoretical AA sequence and to look for genetic variation in the untranslated regions. The aim is to confirm the protein genetic variants previously reported, while searching for additional genetic variation in the CN genes of 30 RDC. We observed genetic variation in 116 SNPs in the known CN genes where 10% of the SNPs are exon variants and the remaining 90% are intron variants. A total of 2.5% of the SNPs are found in the 5′- or 3′-untranslated region (UTR) regions of the exons; 2% are synonymous variants and 6% are missense variants that concurred with the known protein variants for <em>CSN1S1, CSN2</em>, and <em>CSN3</em>. Furthermore, 6% of the SNPs are splice polypyrimidine tract intron variants. The 2 genetic variants in the 5′- and 3′-UTR in <em>CSN1S1</em> and <em>CSN3</em> are found with protein variants <em>CSN1S1C</em> and <em>CSN3B</em>. Because both UTR variants are associated with gain and loss of micro RNA and transcription factors, this could explain differences in expression of the genetic protein variants. Preliminary chi-squared analysis and comparison with previous GWAS studies showed potential connections between the identified SNPs and coagulation properties of milk. By advancing the knowledge of the connection between the DNA sequence and the functional properties of the CN proteins, we hope to learn more about the cheese coagulation properties of milk from RDC.</p></div>\",\"PeriodicalId\":94061,\"journal\":{\"name\":\"JDS communications\",\"volume\":\"5 4\",\"pages\":\"Pages 299-304\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2666910224000267/pdfft?md5=ff57d97b1008b3477a97c2e6185e3cd8&pid=1-s2.0-S2666910224000267-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"JDS communications\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2666910224000267\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"JDS communications","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666910224000267","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
牛奶凝乳酶凝固特性受损可能导致加工时间延长和生产损失。据估计,牛奶凝固性的遗传率为 0.28 至 0.45,这表明遗传选择可用于控制这一性状。CN 蛋白由 CSN1S1、CSN2、CSN1S2 和 CSN3 基因表达,位于牛的第 6 号染色体上。为了更好地了解 CN 基因的遗传变异对牛奶凝固性的影响,我们对 30 头凝固性不同的瑞典红奶牛(RDC)的血液和牛奶样本进行了调查。对这 30 头奶牛的 CN 基因进行了 DNA 测序,以确定理论 AA 序列,并寻找非翻译区的遗传变异。目的是确认之前报告的蛋白质遗传变异,同时寻找 30 头 RDC 的 CN 基因中的其他遗传变异。我们在已知的 CN 基因中观察到 116 个 SNP 的遗传变异,其中 10% 的 SNP 为外显子变异,其余 90% 为内含子变异。共有 2.5% 的 SNP 位于外显子的 5′- 或 3′- 非翻译区 (UTR) 区域;2% 为同义变异,6% 为错义变异,与 CSN1S1、CSN2 和 CSN3 的已知蛋白质变异一致。此外,6% 的 SNP 是剪接多嘧啶束内含子变异。CSN1S1和CSN3的5′和3′-UTR中的2个基因变异与蛋白质变异CSN1S1C和CSN3B有关。由于这两个 UTR 变体都与微 RNA 和转录因子的增减有关,这可以解释基因蛋白变体表达的差异。初步的卡方分析以及与以往 GWAS 研究的比较显示,已确定的 SNP 与牛奶的凝固特性之间存在潜在联系。通过进一步了解 DNA 序列与 CN 蛋白质功能特性之间的联系,我们希望能更多地了解 RDC 牛奶的奶酪凝固特性。
Re-sequencing of the casein genes in Swedish Red cattle giving milk with diverse protein profiles and extreme rennet coagulation properties
Impaired rennet coagulation properties in milk could lead to prolonged processing times and production losses. Heritability for milk coagulation has previously been estimated to be 0.28 to 0.45, indicating that genetic selection can be used to manipulate this trait. The CN proteins are expressed by the genes CSN1S1, CSN2, CSN1S2, and CSN3 and are located on bovine chromosome 6. To better understand the effect of genetic variation in the CN genes on milk coagulation, blood and milk samples from 30 Swedish Red Dairy Cattle (RDC) with divergent coagulation properties were investigated. DNA from the 30 cows was sequenced for the CN genes to determine the theoretical AA sequence and to look for genetic variation in the untranslated regions. The aim is to confirm the protein genetic variants previously reported, while searching for additional genetic variation in the CN genes of 30 RDC. We observed genetic variation in 116 SNPs in the known CN genes where 10% of the SNPs are exon variants and the remaining 90% are intron variants. A total of 2.5% of the SNPs are found in the 5′- or 3′-untranslated region (UTR) regions of the exons; 2% are synonymous variants and 6% are missense variants that concurred with the known protein variants for CSN1S1, CSN2, and CSN3. Furthermore, 6% of the SNPs are splice polypyrimidine tract intron variants. The 2 genetic variants in the 5′- and 3′-UTR in CSN1S1 and CSN3 are found with protein variants CSN1S1C and CSN3B. Because both UTR variants are associated with gain and loss of micro RNA and transcription factors, this could explain differences in expression of the genetic protein variants. Preliminary chi-squared analysis and comparison with previous GWAS studies showed potential connections between the identified SNPs and coagulation properties of milk. By advancing the knowledge of the connection between the DNA sequence and the functional properties of the CN proteins, we hope to learn more about the cheese coagulation properties of milk from RDC.