Skip to main content

Whole-Genome Sequencing

Genome-Wide Association Study of Body Size Traits in Luning Chickens Using Whole-Genome Sequencing



Chickens are one of the most economically important animals in the world with a population of over 34.4 billion in 2023 according to Food and Agriculture Organization (FAO) statistics. The broiler industry has evolved significantly over the past century, with a focus on rapid growth rates, efficient feed conversion, and high meat yield. Chicken is the second most numerous meat product in China, and mainly comes from white-feather and yellow-feather chickens. 

With the development of breeding technology, marker-assisted selection (MAS) and genomic selection (GS) have been increasingly utilized in the broiler industry to improve breeding efficiency and enhance target traits. Single-nucleotide polymorphisms (SNPs) and causal genes across the genome can be utilized to accurately estimate each chicken’s genetic potential for specific traits. Therefore, the identification of candidate genetic markers and genes would allow for more accurate and efficient selection of breeding stock, leading to faster genetic improvement and ultimately enhancing the quality and yield of broiler meat for consumers.

Chicken growth traits are well known for their genetic architectural complexity. Currently, there are 5339 chicken quantitative trait loci (QTL) related to the growth traits in the Animal QTL Database (https://www.animalgenome.org/cgi-bin/QTLdb/index, accessed on 24 April 2024). The accuracy and precision of locating QTL depends, in part, on the density of the linkage map created. Unfortunately, the denser the map, the more likely that false positive QTL will be detected with linkage map-based QTL methods. A more precise mapping of traits is possible with newly available genome sequences and genome-wide association studies (GWASs).

The GWAS is a powerful study design that can identify associations between genome-wide sets of genetic variations and a specific trait using genome resequencing or high-density chip technology. This methodology has generated a myriad of robust associations for a range of traits and diseases, and the number of associated variants is expected to grow steadily as GWAS sample sizes increase. With the development of modern breeding technology, GWASs have also been implemented in domestic animals to identify the genetic factors associated with important economic traits. Most of these GWASs were carried out using SNP chips due to high sequencing costs. Whole-genome sequencing (WGS) is a more efficient technology that can detect rare and undiscovered variants. It was more appropriate to explore genomic variation information by WGS with reduced costs.

Luning chickens are mainly located in Mianning County, Sichuan Province, China. As a well-known native breed, Luning chickens have a large body size, and exhibit well-developed chest and leg muscles, high muscle quality, high suitability, and resistance to disease. The increasing market demand has driven the price of Luning chickens to more than 10 times that of ordinary broilers. All the yellow feather broilers used in production are developed from local chicken breeds. Luning chickens are an underutilized genetic resource which needs a systematic evaluation. We aim to cultivate new genetic materials that meet market and industry development needs.

Down syndrome, cystic fibrosis, Huntington's disease, Tay-Sachs disease, Duchenne muscular dystrophy, fragile X syndrome, sickle cell anemia, hemophilia, thalassemia, Marfan syndrome, Turner syndrome, Klinefelter syndrome, phenylketonuria (PKU), neurofibromatosis, spinal muscular atrophy, Prader-Willi syndrome, Angelman syndrome, Rett syndrome, Wilson's disease,

#GeneticDisorders, #DNA, #GeneMutation, #RareDiseases, #DownSyndrome, #CysticFibrosis, #HuntingtonsDisease, #SickleCell, #Thalassemia, #MarfanSyndrome, #PKU, #TurnerSyndrome, #FragileX, #Hemophilia, #MuscularDystrophy, #Neurogenetics, #Genomics, #InheritedDisorders, #MolecularBiology, #PrecisionMedicine


International Conference on Genetics and Genomics of Diseases

Visit: genetics-conferences.healthcarek.com

Award Nomination: genetics-conferences.healthcarek.com/award-nomination/?ecategory=Awards&rcategory=Awardee

Award registration: genetics-conferences.healthcarek.com/award-registration/

For Enquiries: contact@healthcarek.com

Get Connected Here
---------------------------------
---------------------------------
in.pinterest.com/Dorita0211
twitter.com/Dorita_02_11_
facebook.com/profile.php?id=61555903296992
instagram.com/p/C4ukfcOsK36
genetics-awards.blogspot.com/
youtube.com/@GeneticsHealthcare

Comments

Popular posts from this blog

Genetics role in ovarian cancer

The Medical Minute: Genetics play big role in ovarian cancer In 2024, about 19,680 women in the United States will receive a new diagnosis of ovarian cancer and 12,740 women will die from the disease, said Dr. Shaina Bruce , a gynecologic oncologist at Penn State Cancer Institute . The median age of all patients who develop ovarian cancer is 63. Historically, women at increased risk for ovarian cancer are recommended to have their fallopian tubes and ovaries removed when they have completed having children. Taking that step to protect themselves comes at a heavy price ― surgical menopause. But Bruce said medical science is catching up with ovarian cancer. Studies could lead to new methods for preventative care and the surgery needed to lower risk may be easier than it once was. Below, during Gynecologic Cancer Awareness Month, Bruce discusses the disease and why acting to reduce your risk is worth it. What’s the connection between heredity and ovarian cancer? About 25% of all cases of ...

X chromosome

Gene on the X chromosome may help explain high multiple sclerosis rates in women Brain inflammation may be fueled by a gene on the X chromosome, a new study in mice suggests. And in female mice, who carry two X chromosomes, a diabetes drug called metformin may work to counteract that inflammation. If these findings bear out in later studies, they could help to unravel the long-standing mystery of why women, who have two copies of this inflammation-driving gene, are more prone to certain autoimmune diseases, particularly after menopause. A disparity between the sexes Our bodies are patrolled by immune cells that provide protection against bacteria and viruses, but sometimes, these defenses turn on us. In the autoimmune disorder multiple sclerosis (MS), for instance, the immune system attacks myelin, the fatty insulation surrounding the nerve fibers in the brain and spinal cord. This leads to symptoms such as muscle weakness and difficulty walking, as well issues with memory and thinking...

Multifactorial Genetic Conditions

Multifactorial Genetic Conditions Multifactorial genetic conditions are disorders caused by the combined effects of multiple genes and environmental factors , rather than a single gene mutation . These conditions do not follow classic Mendelian inheritance patterns and instead result from complex gene–environment interactions . Factors such as lifestyle, nutrition, infections, stress, and exposure to toxins can significantly influence disease onset and severity in genetically susceptible individuals. Common examples include diabetes, cardiovascular diseases , neural tube defects, asthma, and many neuropsychiatric disorders. Understanding multifactorial inheritance is essential for risk prediction, preventive medicine, and personalized healthcare strategies. Multifactorial inheritance, polygenic traits, gene–environment interaction, complex diseases, genetic susceptibility, environmental risk factors, non-Mendelian inheritance, disease predisposition, polygenic risk score, precision ...