Abstract
In this study, genome-wide association study (GWAS) was conducted for identifying significantly associated genomic regions/SNPs with milk protein and minerals in the 96 taurine-indicine crossbred (Vrindavani) cows using 50K SNP Chip. After quality control, a total of 41,427 SNPs were retained and were further analyzed using a single-SNP additive linear model. Lactation stage, parity, test day milk yield and proportion of exotic inheritance were included as fixed effects in GWAS model. Across all traits, 13 genome-wide significant (p < 1.20 x 10−06) and 49 suggestive significant (p < 2.41 x 10−05) SNPs were identified which were located on 18 different autosomes. The strongest association for protein percentage, calcium (Ca), phosphorus (P), copper (Cu), zinc (Zn), and iron (Fe) were found on BTA 18, 7, 2, 3, 14, and 2, respectively. No significant SNP was detected for manganese (Mn). Several significant SNPs identified were within or close proximity to CDH13, BHLHE40, EDIL3, HAPLN1, INHBB, USP24, ZFAT, and IKZF2 gene, respectively. Enrichment analysis of the identified candidate genes elucidated biological processes, cellular components, and molecular functions involved in metal ion binding, ion transportation, transmembrane protein, and signaling pathways. This study provided a groundwork to characterize the molecular mechanism for the phenotypic variation in milk protein percentage and minerals in crossbred cattle. Further work is required on a larger sample size with fine mapping of identified QTL to validate potential candidate regions.
Introduction
Milk and dairy products are considered a nutrient-rich diet, consisting of fat, protein, lactose along with several essential micronutrients including vitamins and minerals. Minerals representing a small fraction (~9 g/L) of bovine milk, are important for nutritional and technological properties of milk (1). The minerals in milk are present either as an inorganic ion (soluble phase) or form colloidal complexes with organic matter such as proteins, carbohydrates, and ligands including amino acids and citrates (2, 3).
Minerals play an important role in several physiological and biological activities. For instance, calcium, phosphorus, and magnesium are involved in the development of connective tissues such as bones, muscles, cartilages, and teeth in humans (4). Calcium has been reported to play an important role in reducing cholesterol absorption, and in regulating blood pressure in humans (5). The zinc, manganese, iron, and copper are important components of several enzymes and play role in the immune system (6). These elements also serve as catalysts for many biochemical processes such as muscle contraction, nervous transmission, and nutrient absorption (7).
The concentration of milk minerals influences the stabilization of casein micelle in milk. Calcium, phosphorus, and magnesium are an important components of casein micelle and positively regulates the coagulation properties of the milk (8). The milk minerals are complex traits, influenced by both genetic and non-genetic factors, including nutrition, lactation stage, parity, season, and breed (9). Studies have shown that milk minerals have low to moderate heritability for Cu, Zn, Fe, and Mn (10); and moderate to high heritability for Ca, P, and Zn (1). This provides the possibility to alter the concentration of bovine milk minerals through selective breeding.
The genome-wide association studies may improve our understanding of the genetic architecture and underlying molecular mechanism for variation in protein and minerals content in bovine milk. Studies have revealed about several potential candidate genes associated with milk protein percentage in different cattle breeds (11, 12). However, for milk minerals only a limited number of genome-wide association studies has been reported (1, 3). Thus, the aim of this study was to identify genomic regions associated with milk protein percentage (%) and milk minerals including Ca, P, Cu, Zn, Fe, and Mn in Vrindavani cattle, a tropically adapted composite crossbred breed of dairy cattle of India.
Materials and Methods
Animals and Phenotypes
Morning milk samples (50 ml) were collected from 96 crossbred Vrindavani cattle of the ICAR-Indian Veterinary Research Institute, Bareilly. Vrindavani is a composite breed developed at Indian Veterinary Research Institute by crossing indicine (Hariana) with three taurine breeds (Holstein, Brown Swiss, and Jersey). Details of population structure and synthetic breed information of the Vrindavani population were described in a prior study by (13). The cows were kept in a loose housing system with free-stall dairy barn, fed ad libitum with mixed ration, and milked in a free-stall barn using automated milking systems. The cows were in milk (24-403 days) and from parity 1-8.
The protein percentage in milk was determined using a LactoScan milk analyzer (10). The milk minerals (Ca, P, Cu, Zn, Fe, and Mn) were estimated using Flame Atomic Absorption Spectrometer in technical triplicate samples. For the mineralization of milk samples, 5 ml of milk were dried in silica crucible using a hot-air oven. The dried samples were ashed using a muffle furnace. The ashed sample was mixed with 15 ml 1:1 diluted HCl and heated to dissolve the acid-soluble portion of total ash. The soluble portion was filtered and diluted to 100 ml using double distilled water. The digested samples were analyzed, using a flame atomic absorption spectrophotometer (14).
Genotyping and Quality Control
Blood samples were collected from individual cows, with the approval from the Institutional Animal Ethics Commit- tee (IAEC) on ICAR-Indian Veterinary Research Institute, Bareilly. Genomic DNA was isolated using Qiagen DNeasy Blood Mini Kit (Qiagen, Valencia, CA) according to the manufacturer's instructions. The quality and quantity of DNA were evaluated using NanoDrop spectrophotometer, agarose gel electrophoresis and Qubit fluorometer. The extracted genomic DNA were genotyped using Illumina BovineSNP50 Bead Chip platform (Illumina Inc., San Diego, CA) consisting of 53,218 SNPs across the genome. The quality control of the SNP genotypes was performed using PLINK v 1.9 (15). SNPs with call rate <90%, minor allele frequency (MAF) <0.05 and significantly deviating from the Hardy-Weinberg equilibrium were excluded from the analysis. A total of 41,427 SNPs mapping autosomes were retained for further downstream analysis.
Statistical Analyses
Prior to GWAS, the admixture profile and the level of exotic inheritance of individual animal was estimated using ADMIXTRE V.13.0 (16) using a reference panel of purebred taurine (Holstein-Friesian, Brown Swiss, and Jersey) and indicine (Hariana) cattle downloaded from WIDDE (http://widde.toulouse.inra.fr/widde/widde/main.do?module=cattle) and KRISHI (https://krishi.icar.gov.in/jspui/handle/123456789/31167) web portals. The fixed effect of lactation stage, parity, test day milk yield, and the proportion of exotic inheritance (percentage of Holstein-Friesian, Jersey and Brown Swiss, estimated by admixture analysis) were tested with lm function in R. A single-SNP linear regression of phenotype on genotype was fitted for GWAS analysis using snpStats package in R following Gondro (17). The genotypes were tested for additive effect using model.
Where y is the vector of phenotypic observations; X is an incidence matrix relating the phenotypes to the fixed effects including lactation stage, parity, test day milk yield, and the level of exotic inheritance computed by admixture analysis; β is the vector of fixed effects; Z is incidence matrix of genotypes (0 for the first homozygote AA; 1 for the heterozygote AB or BA; 2 for the second homozygote BB) of the fitted SNP; α is the vector of effects of the regression coefficient for SNPs, and e is the vector of residual effects with a normal distribution N ~ (0, I), where is the residual variance.
The Bonferroni correction using 0.05/N, where “N” is the number of SNPs, was applied to the genome-wide significance threshold (18). The SNP effects were declared significant at a genome-wide level of P = 1.20 x 10−06 (0.05/41,427). Since Bonferroni correction was stringent, a suggestive significance threshold of P = 2.41 x 10−05 (1/41,427) was calculated (19). Association between individual SNPs and each trait are shown in the Manhattan plot using R.
The Ensembl database UMDv3.1 (https://www.ensembl.org/Bos_taurus/Info/Annotation) was used to search for genes flanking a region of 500 kb from the genome-wide significant and suggestive SNPs using BEDtools (20). Candidate genes close or containing significant SNPs were analyzed for functional enrichment using DAVID 6.8 (21). The significantly enriched pathways were identified based on enriched scores.
Results and Discussion
The descriptive statistics for protein percentage and 6 individual minerals (Ca, P, Cu, Mn, Zn, and Fe) in the milk of Vrindavani cattle are presented in Table 1. A total of 9 (2 genome-wide and 7 suggestive) significant SNPs for protein percentage; and 53 (11 genome-wide and 42 suggestive) significant SNPs for six different mineral traits were identified.
Table 1
| Traits | Mean | SD | Min | Max | CV |
|---|---|---|---|---|---|
| Protein percentage(%) | 2.814 | 0.193 | 2.480 | 4.170 | 6.859 |
| Ca(mg/l) | 1,471 | 589 | 681 | 2,960 | 40.015 |
| P(mg/l) | 1,192 | 319 | 602 | 2,360 | 26.762 |
| Zn(mg/l) | 3.694 | 1.526 | 1.130 | 7.773 | 41.310 |
| Cu(mg/l) | 0.892 | 0.709 | 0.130 | 2.213 | 79.442 |
| Fe (mg/l) | 8.925 | 4.423 | 3.180 | 22.400 | 49.560 |
| Mn(mg/l) | 0.794 | 0.350 | 0.180 | 1.930 | 44.121 |
Descriptive statistics for protein percentage (%) and mineral (Ca, P, Cu, Mn, Zn, and Fe) in the Vrindavani milk.
Protein Percentage
For protein percentage, two genome-wide significant SNPs (p < 1.20 x 10−06) and 7 suggestive significant SNPs (p < 2.41 x 10−05) were detected on BTA 3, BTA 6, BTA18, and BTA22 (Figure 1; Table 2). Of these, four significant SNPs found on BTA18 (7.63-99.15Mb) includes Beta-carotene oxygenase 1(BCO1), C-Maf inducing protein (CMIP), N-terminal EF-hand calcium binding protein 2 (NECAB2), Cadherin 13 (CDH13), oxidative stress induced growth inhibitor 1 (OSGIN1) and Solute carrier family 38 member 8 (SLC38A8) genes.
Figure 1
Table 2
| SNP | BTA | Position | P-value | Nearest candidate gene |
|---|---|---|---|---|
| ARS-BFGL-NGS-73708 | 18 | 8037156 | 2.16 x 10−07 | BCO1, CMIP |
| ARS-BFGL-NGS-85875 | 18 | 9948949 | 1.06 x 10−06 | NECAB2, CDH13 |
| ARS-BFGL-NGS-39549 | 18 | 9915057 | 1.62 x 10−06 | OSGIN1, SLC38A8 |
| Hapmap24079-BTA-136416 | 22 | 21000933 | 4.25 x 10−06 | BHLHE40 |
| Hapmap33287-BTC-032371 | 6 | 33026144 | 1.00 x 10−05 | - |
| Hapmap33121-BTC-033043 | 6 | 33441527 | 1.24 x 10−05 | - |
| Hapmap52589-rs29020496 | 18 | 7630875 | 1.24 x 10−05 | CENPN, CMC2 |
| ARS-BFGL-NGS-1337 | 3 | 113666410 | 1.41 x 10−05 | USP 40, ATG16L1 |
| BTB-00158861 | 3 | 113701688 | 2.28 x 10−05 | MROH2A, UGT1A1 |
Genome-wide and suggestive significant SNPs for protein percentage in Vrindavani milk.
Minerals
Among minerals, a total of 4, 17, 10, 7, and 15 significant SNPs were detected for Ca, P, Cu, Zn, and Fe, respectively. However, no significant SNP was detected for Mn (Figures 2A-F; Table 3).
Figure 2
Table 3
| Minerals | SNP | BTA | Position | P-value | Nearest candidate gene |
|---|---|---|---|---|---|
| Ca | BTB-01363189 | 7 | 86130978 | 8.20 x 10−08 | HAPLN1, VCAN |
| Ca | BTB-00005259 | 7 | 86801082 | 2.29 x 10−07 | EDIL3 |
| Ca | BTB-01259879 | 7 | 89658972 | 2.29 x 10−07 | RASA1 |
| Ca | BTB-00326076 | 7 | 86044835 | 8.72 x 10−06 | XRCC4 |
| P | Hapmap45428-BTA-47987 | 2 | 72214554 | 6.89 x 10−09 | INHBB,CFAP221 |
| P | ARS-BFGL-NGS-85372 | 2 | 72369610 | 5.47 x 10−08 | CFAP221 |
| P | Hapmap39006-BTA-116188 | 2 | 30481073 | 1.03 x 10−06 | SCN9A,SCN1A, SCN7A, TTC21B |
| P | BTB-01987495 | 2 | 29215002 | 1.27 x 10−06 | XIRP2 |
| P | BTB-01902301 | 2 | 59461527 | 3.91 x 10−06 | HNMT |
| P | UA-IFASA-4860 | 16 | 20472340 | 6.17 x 10−06 | ESRRG |
| P | ARS-BFGL-NGS-20615 | 29 | 5085168 | 6.67 x 10−06 | NAALAD2 |
| P | ARS-BFGL-NGS-105277 | 15 | 65530435 | 8.04 x 10−06 | NAT10 |
| P | ARS-BFGL-NGS-20993 | 2 | 70957217 | 9.92 x 10−06 | EN1 |
| P | ARS-BFGL-NGS-109852 | 2 | 61611083 | 1.08 x 10−05 | CXCR4 |
| P | ARS-BFGL-NGS-104967 | 13 | 55642499 | 1.44 x 10−05 | CDH4 |
| P | Hapmap38699-BTA-81626 | 2 | 55831708 | 1.55 x 10−05 | - |
| P | ARS-BFGL-NGS-58619 | 2 | 71779928 | 1.60 x 10−05 | CFAP221 |
| P | ARS-BFGL-NGS-25171 | 21 | 34486610 | 2.01 x 10−05 | ARID3B |
| P | Hapmap60572-rs29010980 | 16 | 78157760 | 2.15 x 10−05 | CRB1 |
| P | Hapmap49377-BTA-91839 | 16 | 21134492 | 2.28 x 10−05 | ESRRG |
| P | ARS-BFGL-NGS-82451 | 16 | 81016831 | 2.37 x 10−05 | CACNA1S |
| Cu | ARS-BFGL-NGS-1062 | 3 | 92082212 | 1.68 x 10−07 | DHCR24, USP 24 |
| Cu | BTB-01155381 | 3 | 79282515 | 3.40 x 10−06 | INSL5 |
| Cu | BTA-59703-no-rs | 25 | 22197501 | 4.73 x 10−06 | CACNG3 |
| Cu | BTB-00280101 | 6 | 110508154 | 7.04 x 10−06 | CLNK |
| Cu | BTA-107777-no-rs | 3 | 73921609 | 9.19 x 10−06 | - |
| Cu | ARS-BFGL-NGS-100916 | 6 | 105095758 | 9.61 x 10−06 | PPP2R2C |
| Cu | BTB-01951920 | 6 | 21332376 | 1.12 x 10−05 | PPA2 |
| Cu | ARS-BFGL-NGS-116643 | 4 | 96258114 | 1.25 x 10−05 | PLXNA4 |
| Cu | Hapmap32870-BTA-162083 | 5 | 14189730 | 1.46 x 10−05 | SLC6A15 |
| Cu | ARS-BFGL-NGS-54036 | 3 | 48734443 | 2.24 x 10−05 | ALG14,ABCD3 |
| Zn | ARS-BFGL-NGS-76248 | 14 | 8879810 | 3.50 x 10−07 | ST3GAL1 |
| Zn | Hapmap31987-BTC-062044 | 14 | 8425401 | 8.59 x 10−07 | ZFAT |
| Zn | UA-IFASA-7842 | 14 | 9472109 | 1.81 x 10−06 | PHF20L1,KCNQ3 |
| Zn | ARS-BFGL-BAC-10375 | 14 | 6616434 | 2.42 x 10−06 | - |
| Zn | Hapmap26527-BTC-005059 | 14 | 4176618 | 4.31 x 10−06 | AGO2, DENND3 |
| Zn | ARS-BFGL-NGS-92308 | 13 | 67081069 | 1.13 x 10−05 | MANBAL |
| Zn | ARS-BFGL-NGS-94105 | 22 | 7691228 | 1.34 x 10−05 | FBXL2 |
| Fe | ARS-BFGL-NGS-96204 | 2 | 65600025 | 3.26 x 10−07 | NCKAP5 |
| Fe | ARS-BFGL-NGS-32707 | 2 | 67078207 | 5.59 x 10−07 | - |
| Fe | BTA-11592-rs29017351 | 2 | 69569936 | 1.75 x 10−06 | CFAP221 |
| Fe | ARS-BFGL-NGS-101411 | 2 | 72163562 | 1.75 x 10−06 | INHBB |
| Fe | ARS-BFGL-NGS-22157 | 2 | 71906695 | 6.42 x 10−06 | TMEM177 |
| Fe | BTB-01536946 | 2 | 68429456 | 6.70 x 10−06 | DPP10 |
| Fe | ARS-BFGL-NGS-29914 | 18 | 42706451 | 7.38 x 10−06 | DPY19L3 |
| Fe | Hapmap40319-BTA-19899 | 2 | 102634206 | 8.86 x 10−06 | VWC2L |
| Fe | ARS-BFGL-NGS-5074 | 18 | 43588701 | 1.10 x 10−05 | RHPN2, FAAP24, LRP3 |
| Fe | Hapmap43494-BTA-122491 | 10 | 94570405 | 1.12 x 10−05 | - |
| Fe | ARS-BFGL-NGS-60714 | 2 | 102060979 | 1.33 x 10−05 | IKZF2 |
| Fe | Hapmap49519-BTA-19205 | 2 | 68058489 | 1.39 x 10−05 | DPP10 |
| Fe | ARS-BFGL-NGS-113875 | 11 | 3106988 | 1.41 x 10−05 | ACTR1B, ZAP70 |
| Fe | ARS-BFGL-NGS-40198 | 10 | 2617295 | 1.41 x 10−05 | YTHDC2 |
| Fe | Hapmap57118-rs29009938 | 24 | 39365195 | 2.35 x 10−05 | EPB41L3 |
Genome-wide and suggestive significant SNPs for minerals (Ca, P, Cu, Zn, Fe, and Mn) in Vrindavani milk.
A total three genome-wide significant and 1 suggestive significant SNPs on BTA7 (86.04-89.65Mb) were found to be associated with Ca. The region contains several genes including Hyaluronan and proteoglycan link protein 1 (HAPLN1), Versican (VCAN), EGF like repeats, and discoidin domains 3 (EDIL3). A total of three genome-wide and 14 suggestive significant SNPs were found to be associated with P. The most significantly (p = 6.89 x 10−09) associated SNP (Hapmap45428-BTA-47987) was located 0.10 Mb downstream from Inhibin subunit beta B (INHBB) gene and 0.81 Mb downstream from Cilia and flagella associated protein 221 (CFAP221) gene on BTA2. Total 1 genome-wide and 9 suggestive significant SNPs were observed to be associated with Cu. The most significantly (p = 1.68 x 10−07) associated SNP (ARS-BFGL-NGS-1062) with Cu was identified at 0.63 Mb downstream from the 24-dehydrocholesterol reductase (DHCR 24) gene on BTA3. The SNP (BTA-59703-no-rs) significantly associated with Cu (p = 4.73 x10−06) on BTA25 was located within Calcium voltage-gated channel auxiliary subunit gamma 3 (CACNG3) gene. A total of 2 genome-wide and 5 suggestive significant SNP were associated with Zn. Out of these 7 SNPs, 5 significant SNPs were located within 5.29 Mb (4.17-9.47 Mb) region of BTA14. The most significant (p = 3.50 x 10−07) SNP (ARS-BFGL-NGS-76248) associated with Zn was located 0.09 Mb upstream from the ST3 beta-galactoside alpha-1 (ST3GAL1) gene. A total of 2 genome-wide and 15 suggestive significant SNPs were significantly associated with Fe. Total six significant SNPs were identified within 4.10 Mb region (65.60-72.17 Mb) on BTA2. The most significant (p = 3.26 x 10−07) SNP (ARS- BFGL-NGS-96204) associated with Fe was located 0.45 Mb away from NCKAP5 gene on BTA2. The most significantly (p = 1.02 x 10−04) associated SNP (Hapmap58269-rs29018185) with Mn was located on BTA 19, although it was below the cut-off threshold level of significance.
The functional enrichment of genes close to significant SNPs was involved in ion transport (GO:0005248), metal ion binding (GO:0005509), integral and transmembrane protein (GO:0086010), and signaling pathway (Supplementary Table S1).
In the present study, several significant SNPs found to be associated with protein percentage and individual mineral concentration in the milk of Vrindavani cattle. To our knowledge, this is the first study to identify genomic regions associated with milk mineral content in composite Vrindavani cattle. Detection of several previously reported genes and genomic regions associated with different milk composition traits indicates their potential role in regulating the concentration of minerals and protein percentage in bovine milk.
For protein percentage, the significant 1.9 Mb region (8.03-9.94 Mb) on BTA 18 was partly overlapping with previously reported QTLs associated with milk coagulation (22). The milk coagulation is directly influenced by the casein composition, which indicates that this region may have the potential to influence the protein percentage in milk (23). This region includes the CDH 13 (Cadherin-13) gene which is expressed in mammary tissues and associated with the protein content of the milk (24).
On BTA2, 18 significant SNPs were identified for P and Fe content. Two significant SNPs associated with P and Fe were 0.10 and 0.35 Mb away from the inhibin subunit beta B (INHBB) gene on BTA2. In humans, INHBB gene plays a major role in regulating calcium and phosphorus during bone formation (25). More specifically, INHBB facilitates interaction with the beta glycan, which stimulates extracellular matrix mineralisation (26). The SNP associated with Fe is located 0.35 Mb downstream from the IKAROS family zinc finger 2 (IKZF2) is involved in metal ion binding (27) and host immune response (28).
On BTA3, three significant SNPs were associated with milk Cu content. Buitenhuis et al. (1) identified several significant SNPs for Cu on BTA3 (91.0-91.3 Mb) in Danish Holstein milk. However, these SNPs do not overlap with the significant SNPs for Cu identified in our study. The most significant SNP associated with Cu is located 0.79 Mb upstream from the Ubiquitin Specific Peptidase 24 (USP24) gene. The USP24 gene belongs to the cysteine proteases family and plays role in protein deubiquitination of the proteins which influences the stability of the casein micelle in the milk (29). However, the role of this gene in the regulation of milk Cu concentration is not known.
On BTA7, four significant SNPs associated with Ca, were located close to HAPLNI, VCAN, and EDIL3 genes. These genes are referred to as calcium-binding proteins (GO:0050850, positive regulation of calcium-mediated signaling) and are involved in tissue calcification and bone mineralization in vertebrates (30). In chickens, the EGF-like repeats and discoidin domains 3 (EDIL3) gene bind with the calcium ion to guide vesicular transportation of minerals during eggshell calcification (31). Even though its role in milk calcium is not known, EDIL3 could be considered as a candidate gene, which warrants fine mapping.
The SNP named Hapmap3 1987-BTC-062044 was significantly (p = 3.50 x 10−07) associated with Zn, is located at 0.12 Mb away from the Zinc finger and AT-hook domain containing (ZFAT) on BTA14, which is involved in the transcription of immune-related genes.
Conclusion
Our study identified several candidate genes associated with milk protein percentage and milk minerals, that are involved in ion transport, signaling pathways via integral protein, transmembrane membranes, zinc-fingers, and metal ion binding. The strongest association for protein percentage was identified on BTA18. Among studied minerals, the strongest association for Ca, P, Cu, Zn, and Fe were found on BTA 7, 2, 3, 14, and 2, respectively. These roles of genes and genomic regions suggested that milk mineral concentration is probably regulated by transportation and homeostasis of ions. These identified variants are a step forward to characterize the molecular mechanism affecting milk minerals in Vrindavani cattle. However, additional validation of detected variants and their association with milk minerals is required on large sample size.
Funding
This project work was supported by the CAAST-ACLH project of NAHEP. AS was recipient of fellowship from ICMR fellowship during her PhD programme.
Publisher's Note
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Statements
Data availability statement
The datasets presented in this study can be found in online repositories. The names of the repository/repositories and accession number(s) can be found at: Figshare, https://figshare.com/articles/dataset/Genotypes/12808343/2.
Ethics statement
The animal study was reviewed and approved by Institute Animal Ethics Committee of Indian Veterinary Research Institute, Bareilly.
Author contributions
AK conceived and designed the experiments. AS and AK performed the experiments, analyzed the data, and wrote the paper. CG, AP, and TD contributed reagents/materials/analysis tools. All authors contributed to the article and approved the submitted version.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fvets.2022.760364/full#supplementary-material
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Summary
Keywords
crossbred cattle, genome-wide association studies, milk minerals, milk protein, Vrindavani
Citation
Singh A, Kumar A, Gondro C, Pandey AK, Dutt T and Mishra BP (2022) Genome Wide Scan to Identify Potential Genomic Regions Associated With Milk Protein and Minerals in Vrindavani Cattle. Front. Vet. Sci. 9:760364. doi: 10.3389/fvets.2022.760364
Received
18 August 2021
Accepted
11 February 2022
Published
10 March 2022
Volume
9 - 2022
Edited by
Sunday O. Peters, Berry College, United States
Reviewed by
George R. Wiggans, Council on Dairy Cattle Breeding, United States; Tara G. McDaneld, U.S. Meat Animal Research Center (USDA), United States
Updates
Copyright
© 2022 Singh, Kumar, Gondro, Pandey, Dutt and Mishra.
This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Amit Kumar vetamitchandan07@gmail.com
This article was submitted to Livestock Genomics, a section of the journal Frontiers in Veterinary Science
Disclaimer
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