Go to Top Go to Bottom
Anim Biosci > Volume 29(1); 2016 > Article
Cahyadi, Park, Seo, Jin, Choi, Heo, Kang, Jo, and Lee: Variance Component Quantitative Trait Locus Analysis for Body Weight Traits in Purebred Korean Native Chicken


Quantitative trait locus (QTL) is a particular region of the genome containing one or more genes associated with economically important quantitative traits. This study was conducted to identify QTL regions for body weight and growth traits in purebred Korean native chicken (KNC). F1 samples (n = 595) were genotyped using 127 microsatellite markers and 8 single nucleotide polymorphisms that covered 2,616.1 centi Morgan (cM) of map length for 26 autosomal linkage groups. Body weight traits were measured every 2 weeks from hatch to 20 weeks of age. Weight of half carcass was also collected together with growth rate. A multipoint variance component linkage approach was used to identify QTLs for the body weight traits. Two significant QTLs for growth were identified on chicken chromosome 3 (GGA3) for growth 16 to18 weeks (logarithm of the odds [LOD] = 3.24, Nominal p value = 0.0001) and GGA4 for growth 6 to 8 weeks (LOD = 2.88, Nominal p value = 0.0003). Additionally, one significant QTL and three suggestive QTLs were detected for body weight traits in KNC; significant QTL for body weight at 4 weeks (LOD = 2.52, nominal p value = 0.0007) and suggestive QTL for 8 weeks (LOD = 1.96, Nominal p value = 0.0027) were detected on GGA4; QTLs were also detected for two different body weight traits: body weight at 16 weeks on GGA3 and body weight at 18 weeks on GGA19. Additionally, two suggestive QTLs for carcass weight were detected at 0 and 70 cM on GGA19. In conclusion, the current study identified several significant and suggestive QTLs that affect growth related traits in a unique resource pedigree in purebred KNC. This information will contribute to improving the body weight traits in native chicken breeds, especially for the Asian native chicken breeds.


Quantitative trait loci (QTLs) are genomic regions associated with quantitative traits. To identify these regions analyses should focus on identifying QTLs that link phenotypic data (quantitative traits) and genotypic data (usually molecular markers) in an attempt to explain the genetic basis of variation in complex traits (Andersson and Georges, 2004). The DNA markers usually used for QTL detection are single nucleotide polymorphisms (SNPs), restriction fragment length polymorphisms (RFLPs), and simple sequence length polymorphisms (SSLPs or microsatellites) (Vignal et al., 2002). For the past several decades, microsatellite markers have dominated animal genome studies, especially in the field of molecular genetics, due to the high allele number at a single microsatellite locus and the possibility to genotype by simple polymerase chain reaction (PCR). The high numbers of alleles allow generation of high values of heterozygosity where the number of reference families can be dramatically reduced to construct the map. Utilization of microsatellite markers has been widely used to map the genome in agricultural animals including chicken, which has made the chicken a valuable organism in genomics studies (Groenen et al., 2000). In addition, microsatellite markers have been valuable in detecting QTL regions for economically important traits in the chicken (Zhang et al., 2011; Wang et al., 2012).
In Korea, genetic improvement of Korean native chicken (KNC) has been a major concern since 1994, when the government established a conservation program dedicated to KNC restoration. This project has been successfully divided the KNC into five lines based on plumage colors consisting of black, gray, red, white and yellow lines (Jin et al., 2014). One of these lines has been used to create a commercial three-way KNC hybrid designated Woorimatdag. Consumer acceptance of KNC has steadily increased due to their superior nutritional contents, taste and unique texture of meat (Jeon et al., 2010). Also, the price of native chicken is approximately twice that of commercial broilers, which has allowed poultry breeders to develop a native chicken industry in Korea (Cahyadi et al., 2013; Seo et al., 2013). However, KNC have some inferior performance (growth-related) traits. As in most native chicken breeds, KNC displays low growth rate and high variation in body weight traits. Therefore, appropriate breeding strategies are required to improve the growth performances of KNC to meet consumer’s demands, so the proportion of imported chicken breeds in the market can be reduced (Cho et al., 2014).
In the present study, microsatellite markers were used to genotype chicken samples and genome-scan analysis was conducted to map QTLs for body weight traits of KNC. Mapping of QTLs using microsatellite markers has been successfully used to determine genetic contributions to economically important traits in chickens by examining the relationship between variations of microsatellite allelic and growth-related traits (Schreiweis et al., 2005; Tercic et al., 2009). Mapping of QTL regions will not be clearly valuable without screening and tracing the positional candidate genes in those QTL regions. For this reason, QTL studies are always followed by detection of mutations in the functional regions within QTL regions. Uemoto et al. (2010) identified a positional candidate gene (the ornithine decarboxylase gene) for growth and carcass weight (CW) in F2 intercross chickens based on a previously determined QTL region on chicken chromosome 3 (GGA3). The retinoblastoma 1 gene in the QTL region for body and CW is also a potential positional candidate gene for body weight (Zhang et al., 2011).
Hence, the present study was performed to map QTLs for body weight traits using variance component linkage analyses and to trace positional candidate genes within those QTL regions in KNC.


Experimental animals

The experimental design used in the present study was F1 nuclear family design comprising two generations (i.e., F0 and F1). A total of 88 F0 that comprises 15 sires and 68 dams has been mated by following within line mating system. Total of 3 sires and 4 to 5 dams for each line have been used to produce 595 F1 progeny (black, 90; gray, 110; red, 135; white, 125; and yellow, 135). These animals were generated under very strict breeding procedure of the National Institute of Animal Sciences (NIAS), Korea. Dams were mated to sires by artificial insemination and matings between sibs were avoided. Additionally, they were maintained and reared under standard feeding and environmental conditions.

Genotypic and phenotypic analyses

The DNA genome was isolated by following the DNA extraction procedure for blood samples (GeNet Bio, Daejeon, Korea). NanoDrop 2000c UV-Vis Spectrophotometer (Thermo Fisher Scientific Inc., Waltham, MA, USA) was used to quantify and to check the quality of extracted DNA. Then, the DNA samples were stored in the refrigerator at −20°C to maintain DNA quality for further analyses. Total of 131 highly polymorphic microsatellite (MS) markers and 8 SNP markers were used to genotype F0 and F1 samples. A total of 27 chromosomes (26 autosomes+Z chromosome) have been covered with the total map length of 2,729.4 centi Morgan (cM) and the average distance between markers was 19.64 cM. These MS markers were selected from the Ark Database (http://www.thearkdb.org/arkdb/) to be genotyped that previously described by Seo et al. (2013). In addition, 8 SNP markers were selected from our candidate genes SNPs data that generated by direct sequencing and genotyped using PCR-RFLP and Fluidigm Genotyping Technology. Detailed information on genetic linkage map was reported by Seo et al. (2015b). Four markers on Z chromosome covering 113.3 cM were not used for QTL analysis; i.e., a total of 135 DNA markers covering 26 autosomes were used in this study.
Phenotypic measured in current study was body weight and growth rate traits. Body weights were observed and recorded at every two weeks from hatch to slaughter age at 20 weeks of age. Weight of half carcass was also measured when slaughter process and evisceration were totally completed.

Quantitative trait loci mapping

The QTL analysis was performed using a variance component based program, SOLAR, for outbred nuclear F1 resource pedigree (Almasy and Blangero, 2010). The identical-by-decent (IBD) matrix was calculated based on the marker and pedigree information. Using this IBD matrix, the logarithm of the odds (LOD) score to test presence of QTL was computed at a 1-cM interval across the genome for each F1 chicken. The IBD matrix is incorporated to a linear mixed model as follows:
(Model 1)
where, y is a vector of the phenotypic values for body weight traits except for the hatch weight; b is a vector of fixed effects including sex, line, and batch; q is a vector of additive QTL effect; u is a vector of residual additive polygenic effects; e is a vector of residual environmental effects; X, Z1, and Z2 are incidence matrices for b, q, and u, respectively. The mean and variance for residual additive polygenic effects can be defined as: u~N (0, Aσa2), where A is the additive genetic relationship matrix computed from the F1 pedigree in this study and σa2 is the residual additive polygenic variance. The mean and variance for additive QTL effects can be defined as: q~N (0, Gσq2), where G is the IBD matrix and σq2 is QTL effect variance. The mean and variance for residual effects can be defined as: e~N (0, Iσe2), where I is the identity matrix and σe2 is residual variance. The variance components were estimated by maximum likelihood method.
A likelihood ratio test using SOLAR was conducted to evaluate the significance of the full model (with random common environmental effects of dam) compared to the reduced model (without random common environmental effects of dam). As a result, the Model 1 was extended further to incorporate the maternal (dam) environmental effect for the hatch weight trait as follows:
(Model 2)
where, y is a vector of the phenotypic values for the hatch weight; m is a vector of random maternal (dam) environmental effects; Z3 is incidence matrix for m. The mean and variance for the maternal (dam) effects can be defined as: m~N (0, Sσm2), where S is the structuring matrix for the maternal (dam) environmental effects and σm2 is variance due to dam.
Thresholds for evaluating significance of QTL were calculated by a numerical method (Piepho, 2001). The threshold levels established by this method vary as a function of the trait studied and the chromosome length. A 1% chromosome-wide threshold for the significant linkage was employed. A suggestive linkage was employed using a 5% chromosome-wide threshold. The 1-LOD drop method was used to estimate the support intervals (SIs) for the identified QTL (Lander and Botstein, 1989).

Screening of positional candidate genes

Positional candidate genes for growth-related traits in the identified QTL region were screened using National Center for Biotechnology Information (NCBI) database (http://www.ncbi.nlm.nih.gov), Ensamble Genome Browser (http://www.ensembl.org). The relevance of all screened positional candidate genes to growth phenotypes was verified using the GeneCards database (http://www.genecards.org). Moreover, SNP markers from the whole genome sequence of KNC (Seo et al., 2015a) were assigned to the selected positional candidate genes. We further screened the candidate genes that included heterozygous SNPs.


Phenotypic analysis

The descriptive statistics of phenotypic traits in F1 population including mean, standard deviation, minimum and maximum values are presented in Table 1. The number of chickens ranged from 584 to 595. The Ryan-Joiner normality evaluation was also performed to ensure all observed data were in normal distribution. To evaluate the significance of random common maternal (dam) environmental effects, a likelihood ratio test was conducted. These maternal effects were significant only for hatch weight (p<0.001). Thus, Model 2 was used for the QTL analysis of hatch weight. Model 1 was used to perform QTL mapping of all other traits, since the dam effects were not significant for other body weight traits (data not shown).

Quantitative trait loci analysis

QTLs that reached suggestive thresholds for body weight, half CW, and growth are summarized in Table 2. Five QTLs influencing growth traits were identified in this F1 resource pedigree of KNC. Among them, two QTLs identified at the 1% chromosome-wide significance levels: GGA 3 for growth 16–18 weeks (GR16-18) (LOD = 3.24) (Figure 1A) and GGA4 for GR6-8 (LOD = 2.88) (Figure 1B). Rest of them were mapped on GGA2, GGA5, and GGA12. Four additional QTLs affecting body weight traits were detected at the 1% (i.e., QTL on GGA4 for BW4) and 5% (i.e., QTLs on GGA3, GGA4, GGA19) chromosome-wide threshold levels. The QTL for body weight at 16 weeks of age (BW16) was identified on GGA3. Similar patterns of QTL curves were found on GGA4 that affected body weight at 4 weeks of age (BW4) and 8 weeks of age (BW8) (Figure 1B). These QTLs were located around 23 to 37 cM on GGA4, where the closest marker to the QTL peak was ADL0203. The patterns of these QTL peaks similarly appeared at early to middle stages of age, and gradually disappeared when body weights were measured at 16 to 20 weeks of age (data not shown). In addition, a QTL for body weight at 18 weeks of age (BW18) was detected on GGA19 between the MCW0266 and MCW0256 markers.
Regarding CW, two suggestive linkage QTLs at the 5% chromosome-wide threshold level were also identified on flanking regions of GGA19 located at 0 and 70 cM. One of these QTLs was in a similar location as the QTL for BW18 (Figure 1C).

Positional candidate genes

The candidate genes were intensively traced just after QTL for the body weight and growth were detected. The screening of the positional candidate genes was carried out on GGA4 since these QTL signal consistently appeared for BW4, BW8 and GR6-8 (Figure 1B). The QTL affecting GR6-8 (LOD = 2.88, nominal p value = 0.0003) was used to screen for a positional candidate gene. The QTL confidence interval was established by the 1-LOD drop method. A positional candidate gene was located in the QTL region for GR6-8 on GGA4. The candidate was the insulin receptor substrate 4 gene (IRS4) that plays an important role in growth, reproduction and glucose homeostasis (Sadagurski et al., 2014).


Two significant (GGA3 and GGA4) and three suggestive (GGA2, GGA5, and GGA12) QTLs for growth were identified. One significant and three suggestive QTLs affecting body weight traits were also detected on three different chromosomes. They comprised a QTL for BW16 on GGA3, two neighboring QTLs located at 23 to 37 cM on GGA4 for BW4 and BW8, and a QTL for BW18 on GGA19. Moreover, two QTLs for CW were also identified at two distal ends of GGA19.
The QTL for GR16-18 on GGA3 showed the highest LOD score (LOD = 3.24, nominal p-value = 0.0001) in this study. Interestingly, similar QTL linkage patterns for BW4, BW8 and GR6-8 on GGA4 were detected (Figure 1B). In fact, there were several non-significant QTLs that showed very similar QTL curve patterns compared to the three identified QTLs (data not shown). The LOD score of those QTLs on GGA4 were also decreased by age and gradually disappeared after 16 weeks of age (data not shown). Therefore, the same QTL (i.e. pleotropic QTL) may affect these traits. However, we cannot exclude the possibility that two closely linked but different QTLs may also affect these two traits. These results indicate that the QTL detected on GGA4 may affect growth traits from early to middle life stages, and those the QTLs on other chromosomes affect body weight traits at different stages of age. Thus, chicken growth and development may involve multiple genes that have roles at different stages of life.
Studies have been conducted to detect QTL for body weights in different chicken populations (Wahlberg et al., 2009; Wang et al., 2012; Sheng et al., 2013). Wang et al. (2012) identified two QTL locations for body weight at 2 to 5 weeks of age, and body weight 8 to 10 weeks of age on GGA3. Ikeobi et al. (2004) reported that GGA3 (where the QTL for BW16 was presently detected) could be a candidate QTL for breast muscle weight. A QTL on GGA19 was identified as an additional QTL affecting BW18 with the nearest marker to the QTL peak being MCW0256. This MS marker was analyzed as a single marker to be associated with body weight at 3 weeks of age in a chicken interline cross (Atzmon et al., 2008). QTL regions on GGA4 were frequently detected in early to middle life of KNC, even though the 5% significance chromosome-wide level was only found for BW4 and BW8. Thus, this QTL region has potential value for the screening of positional growth-related candidate genes, since other studies also reported that the same QTL regions were detected for BW4, BW6, BW8, BW10, and BW12 in different chicken populations (Jacobsson et al., 2005; Wahlberg et al., 2009; Podisi et al., 2013). Other QTL regions were also identified on GGA4 for overall body weight, CW wing weight, drum stick weight, and thigh weight (Ikeobi et al., 2004; Schreiweis et al., 2005; Tsudzuki et al., 2007). Therefore, along with GGA1, GGA4 is implicated as a chromosome that harbors QTLs for growth-related traits (Cahyadi et al., 2014). Regarding the QTLs for CW in KNC, two QTLs were located at 0 and 70 cM on GGA19. Liu et al. (2013) performed a genome-wide association study to identify loci for body composition and meat quality traits in Beijing-You chickens. A QTL for CW was detected on GGA19 located at 1.8 cM. This location is very close to the results of the current study (0 cM) where a QTL for CW was detected in the KNC purebred population. The presently detected QTL for CW located at 70 cM on GGA19 is a novel QTL for CW in the chicken. As for growth, QTL for GR16-18 on GGA3 was revealed as the strongest evidence for linkage in this study. Abasht and Lamont (2007) performed a genome-wide association study to identify loci for fatness in chicken. They could map a QTL for abdominal fat percentage to the similar genomic region of our QTL for GR16-18. Interestingly, significant QTL for GR6-8 was co-localized with QTLs for BW4 and BW8. This result indicated the genetic co-regulation of QTL for body weight and growth.
In this study, the genetic linkage analysis was performed using 135 DNA markers (i.e., 127 MS markers+8 SNP markers) that representing 26 autosomal linkage groups. We could not cover 13 chromosomes in the chicken. Therefore, the QTLs identified in the current study do not account for the whole QTL effects since our genome scan could not cover several micro-chromosomes. In addition, there is lack of coverage on markers in some macro-chromosomes. Thus, we cannot exclude the possibility that these un-covered genome region may harbor additional significant QTLs.
To validate the identified markers in this study, we will search for the positional candidate genes in the QTL regions flanked by the markers. In fact, we have whole genome sequencing data from the five lines of KNC to develop SNP markers in KNC chicken genome (Seo et al., 2015a). After obtaining SNP information of positional candidate genes from whole genome sequence data, we have plans to perform association studies between these SNP markers and growth traits using a low density customized SNP chip assay. We would like to include the SNP markers located within the positional candidate genes for the customized SNP chip. If a marker shows significant association with growth traits, this information can be useful for marker-assisted selection to improve genetic potential of growth traits in KNC.
The investigation of positional candidate genes in QTL regions on GGA4 was performed. All genes in this region were extracted using the Biomart option in Ensembl (www.ensembl.org) and directly screened considering previously published relevant information regarding their roles and functions. Finally, a potential candidate gene, the insulin receptor substrate 4 gene (IRS4), was selected after an extensive manual curation. IRS4 acts as an interface between multiple growth factor receptors possessing tyrosine kinase activity, such as insulin-like growth factor 1 receptor (IGF1R), insulin receptor, and fibroblast growth factor receptor 1 (FGFR1), and plays an important role in development, growth, reproduction, and metabolic homeostasis (Hinsby et al., 2004). In addition, Sadagurski et al. (2014) revealed that IRS4 is involved in severe obesity and energy expenditure in mice. Based on the prior reports, IRS4 could be a promising novel candidate gene for body weight traits in the chicken. To confirm the effect of the IRS4 gene polymorphisms on body weight, an association study among genotypic and phenotypic should be performed.
Although previous studies have reported the efficiency in mapping QTL that accounts for genetic and phenotypic differences between two divergent lines, researches using the F2 intercross (or backcross) design have provided less practical information on whether these QTL present within the commercial population of interest. For the successful implementation of QTL information into selective breeding programs, segregation of QTL needs to be validated within the population of interest. Thus, the identified QTL regions in this study using F1 nuclear pedigree will provide practical information to identify molecular genetic factors that affect desired growth traits within the KNC population. Moreover, this information from this study will contribute to efforts to improve the body weight traits in native chicken breeds, especially Asian native chicken breeds.



We certify that there is no conflict of interest with any financial organization regarding the material discussed in the manuscript.


This study was funded by grants from the Next-Generation BioGreen 21 Program (Project No. PJ008133012014, Rural Development Administration), and the Golden Seed Project (No. 2013005042SB730, Korea Institute of Planning & Evaluation for Technology in Food, Agriculture Forestry & Fisheries), Korea.

Figure 1
Test statistic profiles for body weight and growth traits on GGA3 (A), GGA4 (B), and QTL for body weight (BW) 18 and (carcass weight) CW on GGA19 (C). The y-axis represents the LOD score testing the hypothesis of a QTL in a given genomic position. Marker map with distances between markers in Kosambi centi Morgan (cM) is given on the x-axis. Colored lines represent QTL profiles for each trait. The horizontal thick and thin black lines represent the 1% and 5% chromosome-wide significant thresholds, respectively. GGA, chicken chromosome; QTL, quantitative trait loci; LOD, logarithm of the odds; cM, centi Morgan.
Table 1
Descriptive statistics of body weight, carcass weight and growth in the Korean native chicken population
Trait Abbreviation n Mean SD Minimum Maximum
Body weight at hatch Hatch 595 (0) 38.32 4.97 24 51
Body weight at 2 weeks BW2 588 (7) 143.89 24.71 78 208
Body weight at 4 weeks BW4 593 (2) 265.92 70.47 100 455
Body weight at 6 weeks BW6 595 (0) 426.84 130.96 155 715
Body weight at 8 weeks BW8 593 (2) 607.66 195.47 150 1030
Body weight at 10 weeks BW10 594 (1) 768.27 222.64 250 1305
Body weight at 12 weeks BW12 593 (2) 992.90 278.10 365 1670
Body weight at 14 weeks BW14 594 (1) 1181.00 297.60 450 1920
Body weight at 16 weeks BW16 595 (0) 1383.10 337.20 470 2155
Body weight at 18 weeks BW18 595 (0) 1587.70 347.10 555 2430
Body weight at 20 weeks BW20 595 (0) 1780.90 372.10 625 2675
Carcass weight CW 590 (5) 999.32 240.06 340 1688
Growth hatch-2 weeks GR0-2 588 (7) 105.56 23.58 41 166
Growth 2–4 weeks GR2-4 587 (8) 122.90 48.52 −19 259
Growth 4–6 weeks GR4-6 593 (2) 161.27 66.18 −15 300
Growth 6–8 weeks GR6-8 593 (2) 180.92 72.76 −85 460
Growth 8–10 weeks GR8-10 592 (3) 160.34 69.84 −80 410
Growth 10–12 weeks GR10-12 592 (3) 224.23 93.08 −30 520
Growth 12–14 weeks GR12-14 592 (3) 188.30 91.14 −215 495
Growth 14–16 weeks GR14-16 584 (11) 208.66 78.05 −55 515
Growth 16–18 weeks GR16-18 592 (3) 205.70 109.69 −145 505
Growth 18–20 weeks GR18-20 593 (2) 191.83 73.65 −75 415

SD, standard deviation.

For no. of individuals (n), values in parentheses are the no. of individuals excluded based on ascertainment of normality.

Table 2
Summary of QTL results for growth-related traits in Korean native chicken
GGA1 Trait Position (cM) Marker2 LOD Nominal p value
2 GR12-14 16 MCW0206-MCW0039 1.92* 0.0029
3 BW16 255 ODC-MCW0037 1.89* 0.0032
3 GR16-18 0 MCW0261-MCW0083 3.24** 0.0001
4 BW4 37 ADL0317-MCW0295 2.52** 0.0007
4 BW8 23 ADL0255-MCW0295 1.97* 0.0026
4 GR6-8 19 ADL0255-MCW0295 2.88** 0.0003
5 GR2-4 23 MCW263-ROS013 2.08* 0.0020
12 GR14-16 57 ADL0240-MCW0198 2.03* 0.0022
19 BW18 0 MCW0266-MCW0256 1.57* 0.0071
19 CW 0 MCW0266-MCW0256 1.88* 0.0032
19 CW 70 HSPB1-MCW0287 1.86* 0.0035

QTL, quantitative trait loci; cM, centi Morgan; LOD, logarithm of the odds; GR, growth; BW, body weight; CW, carcass weight.

1 Gallus gallus chromosome.

2 Flanking markers for QTL support intervals estimated by the 1-LOD drop method.

** 1% and

* 5% chromosome-wide significant thresholds were established by a numerical method proposed by Piepho (2001).


Abasht B, Lamont SJ. 2007. Genome-wide association analysis reveals cryptic alleles as an important factor in heterosis for fatness in chicken F2 population. Anim Genet 38:491–498.
crossref pmid
Almasy L, Blangero J. 2010. Variance Component Methods for Analysis of Complex Phenotypes. Cold Spring Harb Protoc. http:/dx.org/10.1101/pdb.top77
crossref pmid pmc
Andersson L, Georges M. 2004. Domestic-animal genomics: Deciphering the genetics of complex traits. Nat Rev Genet 5:202–212.
crossref pmid
Atzmon G, Blum S, Feldman M, Cahaner A, Lavi U, Hillel J. 2008. QTLs detected in a multigenerational resource chicken population. J Hered 99:528–538.
crossref pmid
Cahyadi M, Jo C, Lee JH. 2014. Quantitative trait loci and candidate genes for the economic traits in meat-type chicken. Worlds Poult Sci J 70:329–342.
Cahyadi M, Seo DW, Jin S, Choi N, Park HB, Heo KN, Kang BS, Jo C, Lee JH. 2013. Association of SNPs in ODC and PRDM16 with Body Weight Traits in Korean Native Chicken. Korean J Poult Sci 40:157–162.
Cho ES, Chung WH, Choi JW, Jang HJ, Park MN, Kim N, Kim TH, Lee KT. 2014. Genome-wide copy number variation in a Korean native chicken breed. Korean J Poult Sci 41:305–311.
Groenen MA, Cheng HH, Bumstead N, Benkel BF, Briles WE, Burke T, Burt DW, Crittenden LB, Dodgson J, Hillel J, Lamont S, de Leon AP, Soller M, Takahashi H, Vignal A. 2000. A consensus linkage map of the chicken genome. Genome Res 10:137–147.
pmid pmc
Hinsby AM, Olsen JV, Mann M. 2004. Tyrosine phosphoproteomics of fibroblast growth factor signaling: A role for insulin receptor substrate-4. J Biol Chem 279:46438–46447.
crossref pmid
Ikeobi CON, Woolliams JA, Morrice DR, Law A, Windsor D, Burt DW, Hocking PM. 2004. Quantitative trait loci for meat yield and muscle distribution in a broiler layer cross. Livest Prod Sci 87:143–151.
Jacobsson L, Park HB, Wahlberg P, Fredriksson R, Perez-Enciso M, Siegel PB, Andersson L. 2005. Many QTLs with minor additive effects are associated with a large difference in growth between two selection lines in chickens. Genet Res 86:115–125.
crossref pmid
Jeon HJ, Choe JH, Jung YK, Kruk ZA, Lim DG, Jo C. 2010. Comparison of the chemical composition, textural characteristics, and sensory properties of North and South Korean native chickens and commercial broilers. Korean J Food Sci Ani Resour 30:171–178.
Jin S, Park HB, Seo DW, Cahyadi M, Choi NR, Heo KN, Jo C, Lee JH. 2014. Association of MC1R genotypes with shank color traits in Korean native chicken. Livest Sci 170:1–7.
Lander ES, Botstein D. 1989. Mapping mendelian factors underlying quantitative traits using RFLP linkage maps. Genetics 121:185–199.
crossref pmid pmc pdf
Liu R, Sun Y, Zhao G, Wang F, Wu D, Zheng M, Chen J, Zhang L, Hu Y, Wen J. 2013. Genome-wide association study identifies Loci and candidate genes for body composition and meat quality traits in Beijing-You chickens. PLoS One 8:e61172
crossref pmid pmc
Piepho HP. 2001. A quick method for computing approximate thresholds for quantitative trait loci detection. Genetics 157:425–432.
crossref pmid pmc pdf
Podisi BK, Knott SA, Burt DW, Hocking PM. 2013. Comparative analysis of quantitative trait loci for body weight, growth rate and growth curve parameters from 3 to 72 weeks of age in female chickens of a broiler-layer cross. BMC Genet 14:22
crossref pmid pmc
Sadagurski M, Dong XC, Myers MG, White MF. 2014. IRS2 and IRS4 synergize in non-LepRb neurons to control energy balance and glucose homeostasis. Mol Metab 3:55–63.
crossref pmid pmc
Schreiweis MA, Hester PY, Moody DE. 2005. Identification of quantitative trait loci associated with bone traits and body weight in an F2 resource population of chickens. Genet Sel Evol 37:677–698.
crossref pmid pmc
Seo DW, Hoque MR, Choi NR, Sultana H, Park HB, Heo KN, Kang BS, Lim HT, Lee SH, Jo C, Lee JH. 2013. Discrimination of Korean native chicken lines using fifteen selected microsatellite markers. Asian Australas J Anim Sci 26:316–322.
crossref pmid pmc
Seo DW, Oh JD, Jin S, Song KD, Park HB, Heo KN, Shin Y, Jung M, Park J, Jo C, Lee HK, Lee JH. 2015a. Single nucleotide polymorphism analysis of Korean native chickens using next generation sequencing data. Mol Biol Rep 42:471–477.
crossref pmid
Seo DW, Park HB, Choi NR, Jin S, Yoo CK, Sultana H, Heo KN, Jo C, Lee JH. 2015b. Construction of genetic linkage map using microsatellite and SNP markers in Korean native chicken. Korean J Poult Sci 42:77–86.
Sheng Z, Pettersson ME, Hu X, Luo C, Qu H, Shu D, Shen X, Carlborg O, Li N. 2013. Genetic dissection of growth traits in a Chinese indigenous×commercial broiler chicken cross. BMC Genomics 14:151
crossref pmid pmc
Tercic D, Holcman A, Dovc P, Morrice DR, Burt DW, Hocking PM, Horvat S. 2009. Identification of chromosomal regions associated with growth and carcass traits in an F (3) full sib intercross line originating from a cross of chicken lines divergently selected on body weight. Anim Genet 40:743–748.
crossref pmid
Tsudzuki M, Onitsuka S, Akiyama R, Iwamizu M, Goto N, Nishibori M, Takahashi H, Ishikawa A. 2007. Identification of quantitative trait loci affecting shank length, body weight and carcass weight from the Japanese cockfighting chicken breed, Oh-Shamo Japanese Large Game. Cytogenet Genome Res 117:288–295.
crossref pmid
Uemoto Y, Sato S, Ohtake T, Sato S, Okumura Y, Kobayashi E. 2011. Ornithine decarboxylase gene is a positional candidate gene affecting growth and carcass traits in F2 intercross chickens. Poult Sci 90:35–41.
crossref pmid
Vignal A, Milan D, SanCristobal M, Eggen A. 2002. A review on SNP and other types of molecular markers and their use in animal genetics. Genet Sel Evol 34:275–305.
crossref pmid pmc
Wang SZ, Hu XX, Wang ZP, Li XC, Wang QG, Wang YX, Tang ZQ, Li H. 2012. Quantitative trait loci associated with body weight and abdominal fat traits on chicken chromosomes 3, 5 and 7. Genet Mol Res 11:956–965.
crossref pmid
Wahlberg P, Carlborg Ö, Foglio M, Tordoir X, Syvänen AC, Lathrop M, Gut IG, Siegel PB, Andersson L. 2009. Genetic analysis of an F2 intercross between two chicken lines divergently selected for body-weight. BMC Genomics 10:248–262.
crossref pmid pmc
Zhang H, Liu SH, Zhang Q, Zhang YD, Wang SZ, Wang QG, Wang YX, Tang ZQ, Li H. 2011. Fine-mapping of quantitative trait loci for body weight and bone traits and positional cloning of the RB1 gene in chicken. J Anim Breed Genet 128:366–375.
crossref pmid

Editorial Office
Asian-Australasian Association of Animal Production Societies(AAAP)
Room 708 Sammo Sporex, 23, Sillim-ro 59-gil, Gwanak-gu, Seoul 08776, Korea   
TEL : +82-2-888-6558    FAX : +82-2-888-6559   
E-mail : animbiosci@gmail.com               

Copyright © 2023 by Asian-Australasian Association of Animal Production Societies.

Developed in M2PI

Close layer
prev next