Capture Sequencing to Explore and Map Rare Casein Variants in Goats

نویسندگان

چکیده

Genetic variations in the four casein genes CSN1S1 , CSN2 CSN1S2 and CSN3 have obtained substantial attention since they affect milk protein yield, composition, cheese processing properties, digestibility as well tolerance human nutrition. Furthermore, variants are used for breed characterization, biodiversity, phylogenetic studies. The current study aimed at identification of five domestic goat breeds from Sudan (Nubian, Desert, Nilotic, Taggar, Saanen) three wild species [ Capra aegagrus (Bezoar ibex), nubiana (Nubian ibex (Alpine ibex)]. High-density capture sequencing 33 goats identified total 22 non-synonymous 13 synonymous single nucleotide polymorphisms (SNPs), which nine seven SNPs new. In gene, new SNP ss7213522403 segregated Alpine ibex. ss7213522526, ss7213522558, ss7213522487 were found exclusively Nubian ss7213522477, ss7213522549, ss7213522575 only. ss7213522604 ss7213522610 DNA sequence led to detection variants. New detected alpha S1 Saanen ( ∗ C1), Bezoar J), K), beta kappa caseins F X), S2 all domesticated H), Desert I), or only J K). results show that most novel occur critically endangered This highlights importance preservation this breed. we suggest validating further characterizing

برای دانلود باید عضویت طلایی داشته باشید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Kappa-casein gene polymorphism in Indian goats

The present work was carried out to analyse the κ-casein variants in five Indian goat breeds by SDS-PAGE, PCRRFLP and SSCP method. A total of 152 unrelated blood samples and 102 milk samples belonging to Barbari, Beetal, Marwari, Surti and Local MP (non-descript) goats were used for analysis. SDS-PAGE exhibited κ-casein allele A in all the breeds. Moreover PCR+RFLP analysis also confirmed the p...

متن کامل

Association Analysis of Rare Variants in Sequencing Studies

ZHENGZHENG TANG: Association Analysis of Rare Variants in Sequencing Studies (Under the direction of Dr. Danyu Lin) Recent advances in sequencing technologies have made it possible to explore the influence of rare variants on complex diseases and traits. Large-scale sequencing studies provide the opportunity to examine the proportion of the missing heritability that is attributable to rare vari...

متن کامل

Evaluating rare variants in complex disorders using next-generation sequencing.

Determining the genetic architecture of liability for complex neuropsychiatric disorders like autism spectrum disorders and schizophrenia poses a tremendous challenge for contemporary biomedical research. Here we discuss how genetic studies first tested, and rejected, the hypothesis that common variants with large effects account for the prevalence of these disorders. We then explore how the di...

متن کامل

Sequencing and Bioinformatics Analysis of Kappa-Casein Exon 4 Gene in Iranian Bacterianus and Dromedaries Camels

Kappa-casein, as a major protein component in mammalian milk, plays an essential role in formation and stabilization milk micelles and preventing them from aggregating and therefore, helping to keep calcium phosphate in solution and transfer of calcium and phosphors from animal milk to consumers. Therefore, the objective of the current study was to investigate genetic and phylogenetic analysis ...

متن کامل

Detection of Rare Genomic Variants from Pooled Sequencing Using SPLINTER

As DNA sequencing technology has markedly advanced in recent years(2), it has become increasingly evident that the amount of genetic variation between any two individuals is greater than previously thought(3). In contrast, array-based genotyping has failed to identify a significant contribution of common sequence variants to the phenotypic variability of common disease(4,5). Taken together, the...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

ژورنال

عنوان ژورنال: Frontiers in Genetics

سال: 2021

ISSN: ['1664-8021']

DOI: https://doi.org/10.3389/fgene.2021.620253