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Polymorphisms in Fatty Acid Desaturase 2 Gene are Associated with Milk Production Traits in Chinese Holstein Cows.


ABSTRACT: This study investigated the single nucleotide polymorphisms (SNPs) of Fatty acid desaturase 2 (FADS2) gene and further explored their genetic effects on conventionally collected milk production traits in Chinese Holstein cows using 18,264 test-day records of 841 cows. One missense mutation c. 908 C > T (SNP site in the complementary DNA sequence), which caused an amino acid change from alanine to valine (294Ala > Val), and two 3' untranslated region (UTR) SNPs, c.1571 G > A and c.2776 A > G were finally identified. The SNP c.908 C > T was significantly associated with test-day milk yield, fat percentage and 305-day milk, fat and protein yield. In particular, the T allele of the SNP c.908 C > T showed a significant association with decreased somatic cell score (SCS) in the investigated population. Significant relationship between the SNP c.1571 G > A and 305-day milk yield showed that genotype GG was linked to the highest milk yield. Substituting the allele G for A at the c.2776 A > G locus resulted in a decrease of protein percentage. Our results demonstrated that FADS2 was an interesting candidate for selection to increase milk production and improve resistance against mastitis.

SUBMITTER: Li M 

PROVIDER: S-EPMC7222784 | biostudies-literature | 2020 Apr

REPOSITORIES: biostudies-literature

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Polymorphisms in Fatty Acid Desaturase 2 Gene are Associated with Milk Production Traits in Chinese Holstein Cows.

Li Mingxun M   Gao Qisong Q   Wang Mengqi M   Liang Yan Y   Sun Yujia Y   Chen Zhi Z   Zhang Huimin H   Karrow Niel A NA   Yang Zhangping Z   Mao Yongjiang Y  

Animals : an open access journal from MDPI 20200412 4


This study investigated the single nucleotide polymorphisms (SNPs) of Fatty acid desaturase 2 (<i>FADS2</i>) gene and further explored their genetic effects on conventionally collected milk production traits in Chinese Holstein cows using 18,264 test-day records of 841 cows. One missense mutation c. 908 C > T (SNP site in the complementary DNA sequence), which caused an amino acid change from alanine to valine (294Ala > Val), and two 3' untranslated region (UTR) SNPs, c.1571 G > A and c.2776 A >  ...[more]

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