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Correlation between heart-type fatty acid-binding protein gene polymorphism and mRNA expression with intramuscular fat in Baicheng-oil chicken.

INTRODUCTION

In 2010, Baicheng oil chicken (BOC) was included in the Directory of National Animal Genetic Resources (Amanguli et al., 2014). BOC has gained popularity because of its delicious taste even when cooked traditionally using only salt and water (Gemenggul et al., 2013). The BOC can be classified into three main species: black Baicheng oil chicken (BBOC), silky Baicheng oil chicken (SBOC), and white Baicheng oil chicken (WBOC) (Wang et al., 2013). The BOC has great flavor and colored (mainly black) feathers, SBOC exerts therapeutic effects on gynecological diseases and was believed extinct for decades (Gemenggul et al., 2013). The WBOC is covered with white feathers and thrives at higher altitudes than BBOC and SBOC. The BOC has a history of over 300 years and resides in the townships of Baicheng County, Xinjiang Uygur Autonomous Region, China at an altitude of more than 2,300 m (Amanguli et al., 2014). Considering the the slow growth rate and low feed conversion ratio of BOC, breeders have introduced other species of chicken since the 1940s. The continuous hybridization resulting from the introduction of other varieties has posed a threat on the survival of these thoroughbred chickens (Gemenggul et al., 2013; Wang et al., 2013).

Intramuscular fat (IMF) content is closely associated with the tenderness, juiciness, and special flavor of meat (Pang et al., 2006). The IMF content depends on the balance between the synthesis and degradation of triacylglycerol, the major component of IMF in muscles and is stored within intramuscular adipocytes (Hocquette et al., 2010).

Fatty acid-binding proteins (FABPs) are cytosolic low-molecular-weight proteins that can be classified into at least nine types: liver, myelin, adipocyte, brain, heart, intestinal, epidermal, testis, and ileal (Chmurzynska, 2006). The members of the FABP gene family have different distribution patterns and functions (Ma et al., 2010). Heart-type fatty acid-binding protein (H-FABP) regulates IMF deposition, promotes the intracellular transport and cellular absorption of fatty acids, and facilitates the utilization and storage of fats (Zhang et al., 2013). And A-FABP are markers of intramuscular adipocytes in which IMF is mainly stored (Hocquette et al., 2010).

The H-FABP is located on chicken chromosome 23 and is expressed in several tissues; the cellular function of the H-FABP gene has yet to be elucidated in detail (Tyra et al., 2011). Previous studies revealed that H-FABP influences meat quality and IMF content in chickens (Li et al., 2008; Tu et al., 2010), pigs (Cho et al., 2009), sheep (Zhang et al., 2013) and in cattle (Brandstetter et al., 2002). The mRNA expression of the H-FABP gene significantly varies in the different tissues of sheep (Huang et al., 2006; Zhang et al., 2013) and swine (Li et al., 2007). However, the mRNA expression pattern of this gene in BOC chickens remains unclear to date (Li et al., 2010; Tu et al., 2010). In the present study, we measured H-FABP mRNA expression and IMF content in the breast and leg muscles of BBOC, SBOC and WBOC. This study aims to determine the temporal and spatial mRNA expression patterns of H-FABP and to identify the correlation between H-FABP gene mRNA and IMF content in the three types of BOCs. The results of this study may provide a theoretical foundation for further research on the functions of the H-FABP gene in chickens.

MATERIALS AND METHODS

Animals

All parent chickens were collected from Heiyingshan in Baicheng County, the provenance of BOCs. A total of 720 healthy BOCs, including 240 BBOCs, 240 SBOCs, and 240 WBOCs, with half males and half females on each group, were raised on the ground in the same chamber, and their fathers were brother and their mothers were sister for each group. The BOCs were raised under the same conditions at the experimental station of animals in Tarim University and were provided ad libitum access to food and water. The protocol was accepted by the Tarim University Institutional Animal Care and Use Committee.

Sample harvest

In total, 30 male and 30 female chickens from each group were slaughtered through avascularization at 30, 60, 90, and 120 d with the same interval, which could display more clear temporal and spatial mRNA expression patterns of H-FABP, and IMF content trends. Breast muscles and leg muscles were collected and then stored at -20[degrees]C for IMF content mensuration and at -80[degrees]C for RNA extraction.

Intramuscular fat content

The IMF content (expressed as weight percentage) was measured using the Soxhlet petroleum-ether extraction method in accordance with the Chinese National Standards GB/T 5009.6.2004, and the results of IMF content were displayed as weight percentage.

Design and synthesis of the primers

Primers were designed to amplify the second exon of H-FABP by Primer 5.0 according to the H-FABP sequence of Gallus gallus (GenBank accession No. AY648562): H-FABP, 5'-CGACAAGGCGACGGTGAA-3' (forward) and 5'-TGGGGCAGGAAGGAGTTT-3' (reverse). Total genomic DNA was abstracted from blood of wing vein by a MasterPure DNA Purification Kit (Beijing SinoGene Scientific Co. Ltd., Beijing, China) following the attached protocol. PCR reaction was performed in a 20 [micro]L system containing 0.5 [micro]L Primer (10 [micro]M), 8 [micro]L ddH2O, 1 [micro]L gDNA, and 10 [micro]L 2 x SG PCR MasterMix (Beijing SinoGene Scientific Co. Ltd., China). The PCR amplification protocol was 94[degrees]C for 3 min, followed by 35 cycles of 94[degrees]C for 30 s, 60[degrees]C for 30 s and 72[degrees]C for 30 s, and a final extension at 72[degrees]C for 10 min. The PCR products were detected on 1% agarose gel. Fifty [micro]L expansion system was carried out in order to recover the products.

The expected size PCR products were analyzed by the technique of polymerase chain reaction-single strand conformation polymorphism (PCR-SSCP). The PCR products were diluted with PCR-SSCP buffer including 0.1% xylene cyanol in formamide and 0.1% bromophenol blue. The mixtures were degenerated at 98[degrees]C for 10 min and cooled in ice for 5 min, and then transferred to a 12% polyacrylamide gel and a 10* TBE buffer. The gels were performed at 4[degrees]C for 250 V, 10 min and 56 V, 16 h. The gels were stained according to a standard protocol (Wang et al., 2007).

RNA extraction and reverse transcription

Total RNA was extracted using Trizol reagent (Invitrogen, Carlsbad CA, USA). The quality and quantity of the isolated RNA were assessed by BioPhotometer (Eppendorf, Hamburg, Germany) and 2% gel electrophoresis, followed by reverse transcription. The 20 [micro]L reverse transcription reaction system comprised the following: 2 [micro]g of RNA, 1 [micro]L of Oligo (dT) 15 Primer, 1 [micro]L of random primers, 10 [micro]L of nuclease-free water, 1 [micro]L of GoScript TM Reverse Transcriptase, 1.6 [micro]L of nuclease-free water, 0.4 [micro]L of Recombinant RNasin Ribonuclease Inhibitor, 4 [micro]L of GoScript TM 5x reaction buffer, 2 [micro]L of Mg[Cl.sub.2] (25 mM), and 1 [micro]L of PCR Nucleotide Mix. The reaction procedure was performed under the following conditions: denaturation for 5 min at 70[degrees]C, annealing for 5 min at 25[degrees]C, extending annealing for 60 min at 42[degrees]C, inactivated reverse transcriptase for 15 min at 70[degrees]C, and then storage at 4[degrees]C.

Real-time polymerase chain reaction

The mRNA expression level of H-FABP was measured using a 7500 Real-Time PCR System with a 20 [micro]L reaction system containing the following: 1 [micro]L of cDNA, 10 [micro]L of 2x SYBR Premix DimerEraser, 0.6 [micro]L of each genespecific primer (100 nM), and 0.4 [micro]L of ROX (passive reference dye). The reaction procedure was performed as follows: 1 cycle of 95[degrees]C for 30 s; 39 cycles of 95[degrees]C for 5 s, 60[degrees]C for 30 s, and 72[degrees]C for 60 s; and 1 cycle of 95[degrees]C for 15 s, 60[degrees]C for 60 s, 95[degrees]C for 30 s, and 60[degrees]C for 15 s. [beta]-Actin was used as the house-keeping gene. The following primers, which were designed through Oligo 6.0 and Primer 5.0 and synthesized by Invitrogen Corporation, were used: H-FABP, 5'-CAGAAGTGGGATGGGAAGGAGA-3' (forward) and 5'-TCATAGGTGCGGGTGGAGAC-3' (reverse); [beta]-actin, 5'-AACACCCACACCCCTGTGAT-3' (forward) and 5'-TGAGTCAAGCGCCAAAAGAA-3' (reverse). The relative expression of these genes was calculated by the [2.sup.-[DELTA][DELTA]Ct] method (Li et al., 2012).

Statistical analysis

POPGENE software (ver.1.31) was used to analyze the frequencies of alleles and genotypes, and the polymorphic information content (PIC) was analyzed by PowerMaker software (ver.3.25). The association between the polymorphism of H-FABP gene and IMF content was performed by SAS statistical software package, version 9.0 (SAS Institute, Inc., Cary, NC, USA) using the SAS software PROC general linear model procedures to determine the significance.

Y = [mu] + G + S + f + h + e

Here Y = the dependent variable, [mu] = the population mean, G = fixed effects of breed, S = fixed effects of sex, f = family, h = random effects, and e = random error. The interaction GxS was not significant for any trait and therefore was not included in the model. The data of IMF and mRNA [MATHEMATICAL EXPRESSION NOT REPRODUCIBLE IN ASCII] were analyzed through the method of one-way analysis of variance analysis and the association between IMF and mRNA ([2.sup.-[DELTA]Ct]) (Tu et al., 2010) were analyzed using Pearson's correlation coefficient both performed with SPSS 17.0 software (American SPSS Corporation, headquartered in Chicago).

RESULTS

Intramuscular fat content

The changes in IMF content with age in the different tissues are shown in Figure 1 and 2. Significant differences in IMF content were observed between 120 and 30 d in the breast muscles of BBOC (p = 0.031) and WBOC (p = 0.027) as well as in the leg muscles of BBOC (p = 0.001), SBOC (p = 0.029), and WBOC (p = 0.019). Significant differences were also detected between 120 and 60 d in the leg muscles of BBOC (p = 0.005) and WBOC (p = 0.040). Moreover, significant differences were found between 90 and 30 d in BBOC (p = 0.033).

Genotype and allele frequency

Three genotypes of H-FABP gene second extron following AA, AB, and BB were detected by PCR-SSCP strategy. The genotypes of AA and BB were sequenced and compared with the sequence AY 648562 acquired from Genbank, respectively. Two mutation sites were detected in BOC, the G939A site created AA genotype and G956A site created BB genotype. Genotypic frequency and gene frequency were showed in Table 1. BB was dominant genotype and B was dominant allele in BBOC, meanwhile, AA was dominant genotype and A was dominant allele in both SBOC and WBOC in natural selection. Parameters of genetic polymorphism were displayed in Table 2. The x2 value were 2.676 (p = 0.102) in BBOC, 3.593 (p = 0.058) in SBOC and 1.839 (p = 0.175) respectively. The population of BOCs fitted with Hardy-Weinberg equilibrium.

Correlation between H-FABP gene polymorphism and intramuscular fat content

The results of correlation between H-FABP gene polymorphism and IMF content of breast muscle and leg muscle were showed in Table 3 and 4, respectively. The results of the least square mean showed that the content of IMF in AA genotype in breast muscle of BBOC was significantly higher than that of AB (p = 0.0176) and the genotype in leg muscle of WBOC was significantly higher than that of AB (p = 0.0145).

mRNA expression of the H-FABP gene

The changes in the mRNA expression of the H-FABP gene with time in the different tissues are shown in Figure 3 and 4. Significant differences in H-FABP mRNA expression were detected between 30 and 120 d in the breast muscles of BBOC (p = 0.001), SBOC (p = 0.007), and WBOC (p < 0.001) as well as in the leg muscles of BBOC (p < 0.001), SBOC (p < 0.001), and WBOC (p < 0.001). Significant differences were also examined between 60 and 120 d in the breast muscles of SBOC (p = 0.042) and in the leg muscles of BBOC (p = 0.007) and WBOC (p = 0.044). Significant differences were observed between 30 and 90 d in the breast muscles of BBOC (p = 0.01), SBOC (p = 0.048), and WBOC (p < 0.001). Moreover, significant differences were detected between 30 and 60 d in the breast muscles of WBOC (p < 0.001) and in the leg muscles of BBOC (p < 0.001), SBOC (p < 0.001), and WBOC (p = 0.001). Finally, a significant difference was found between 60 and 90 d in the leg muscles of BBOC (p < 0.001).

Association between intramuscular fat content and HFABP mRNA expression

The correlation coefficient between IMF and H-FABP mRNA is shown in Table 1. The two parameters were negatively correlated in every muscle of the different types of BOCs. A significant correlation was detected in the leg muscles of WBOC (p = 0.035).

DISCUSSION

The H-FABP is a vital candidate gene for meat quality and promotes fat transportation, utilization, and storage (Zhang et al., 2013). The H-FABP is often found in heart and skeletal muscle tissues, where high fatty acid oxidation occurs; it participates in the delivery of fatty acids to the mitochondria, where [beta]-oxidation occurs (Heuckeroth et al., 1987). Restriction fragment length polymorphism of HFABP affects IMF content and thus has been used as a marker for selecting increased IMF and growth in swine (Gerbens et al., 1999; Gerbens et al., 2001). Saez et al. (2009) found A-FABP gene expression and protein were significantly related with IMF content in ducks. It was reported that the BB genotype at A-FABP had significantly higher IMF content in leg muscles and breast muscles than that in AA and AB genotype in Beijing-You chickens (Ye et al., 2009). In this study we focused on H-FABP, because it has been confirmed that H-FABP is most important among genes which affect fat content and fatty asid metabolism of chickens (Li et al., 2010).

The increasing of IMF content plays an economic important part in chicken breeding (Ye et al., 2009). However, IMF is seldom used as a selection objective in traditional chicken breeding, because it can't be measured in live chickens (Gardan et al., 2007; Ye et al., 2009). The marker-assisted selection provides more advantages than traditional breeding methods for this special parameter (Ye et al., 2009; Tu et al., 2010). So one aim of the current study was to investigate whether mutational cites of H-FABP gene second extron could be used to select IMF content of BOC, thus providing basic data for chicken breeding.

The BBOC has been selected for eggs and meat for a period of time and is most popular at locality, SBOC has been selected for treatment of gynecological diseases, and WBOC is main living at the high altitudes because of their chill-proof. The highest IMF content of breast muscles and leg muscles were found in BOC. These findings are consistent with the popularity of the three chickens in the market.

The PIC was at the range of 0.25<PIC<0.5 in BOCs, which indicated that these three groups were moderate polymorphism. Several SNPs of H-FABP in chickens have been detected and the genotype of H-FABP has been proved to affect the content of IMF in several chicken breeds (Wang et al., 2007; Ye et al., 2009). In the current study, the IMF content of AA genotype in breast muscle of BBOC and in leg muscle of WBOC were significantly higher than those in AB genotype. These results indicated that the G939A site could be taken as marker for higher IMF content selecting for breast muscle of BBOC and leg muscle of WBOC in breeding program. The H-FABP has been isolated from kinds of tissues such as cardiac muscle, skeletal muscle, lung, aorta, brain, adrenal gland, renal cortex, mammary gland, ovary, placenta and adipose tissue (Bai et al., 2013). There are several reports on H-FABP gene mRNA expression (Tyra et al., 2011). These data indicate that H-FABP has a wider biological function than expected (Pang et al., 2006). In these reports, it is common that it was mainly expressed in cardiac muscle, chest muscle and leg muscle (Zschiesche et al., 1995; Gerbens et al., 1999; Tu et al., 2010), results of mRNA expression in present study further proved their conclusions.

In the present study, the expression profiles of the HFABP gene were determined in the breast and leg muscles of BOCs, and the correlation between mRNA expression and IMF content was analyzed. This analysis was based on the relevance of this gene with lipid metabolism and its effect on fatness parameters (Li et al., 2007) and IMF content (Tyra et al., 2011). Although H-FABP expression in muscles correlates with the absorption and transport of fatty acids in cells, it is not associated with adipogenesis (Tyra et al., 2011).

The assay of real- time PCR had been used to measure the transcription level of interesting genes because of its sensitivity and specificity (Tu et al., 2010; Chen et al., 2011). It was reported that H-FABP mRNA expression of an oxidative muscle was higher than that of a glycolytic muscle in cattle (Brandstetter et al., 2002). The mRNA expression level of H-FABP is higher in subcutaneous adipocytes than in intramuscular adipocytes in different tissues of growing pigs at both 80-day-old and 210-day-old; what's more, transcript levels isolated from subcutaneous adipocytes at 80-day-old was higher than that isolated from intramuscular adipocytes at 210-day-old (Gardan et al., 2007). Ontogenesis stages (fetus, 7-day-old, and 5-month-old) significantly affect the mRNA expression of H-FABP in porcine (Li et al., 2007). H-FABP mRNA level peaks in the subcutaneous fat near the wither, then in the visceral fat of perienal, visceral fat of omental, and subcutaneous fat near the base of the tail of Lanzhou fat-tailed sheep (Bai et al., 2013). In chickens, H-FABP influences fat content and fatty acid metabolism (Li et al., 2010). The H-FABP mRNA level in chicken varies depending on breed, tissues in which the mRNA expression level is examined, and age. Many researchers investigated the effects of tissue type or animal age on mRNA expression. However, there is no one report about BOC. In the present study, we focused on the effects of both tissue type and animal age on the mRNA expression of H-FABP. An analysis in chest and thigh muscles has shown that the mRNA expression level of H-FABP peaks at 30 d and then decreases with age. Similarly, Tu et al. (2010) found that the H-FABP mRNA expression at 56 d is higher than that at 120 d. Rump et al. (1996) proved that H-FABP protein level is high in the skeletal muscle of mice during the first days after birth and can remain high up to 30 d. This observation can be attributed to the differentiation of skeletal muscle cells, that is, the transformation of myoblasts into myotubes (Tyra et al., 2011), and they indicate that the H-FABP transcript abundance in semimembranosus and longissimus dorsi muscles of all the researched breeds (Duroc, Pietrain, Pulawska, Polish Large White, and Polish Landrace) of all onto genesis stages (60-, 90-, 12, 50, 180- and 210-d-old) do not exhibit any siginificant changes. Li et al. (2007) observed the mRNA expression levels of H-FABP at the fetus, 7-day-old, and 5-month-old stages of pig ontogenesis and found that age significantly affects H-FABP mRNA expression level, so they considered that the H-FABP gene played an important part in adipose tissue development and function in the swine.

The H-FABP influences IMF content (Li et al., 2007). The present results showed that the mRNA expression of the H-FABP gene negatively affects the IMF contents in the chest and leg muscles of BOCs. Similar results were observed in Rugao and Luyuan chickens (Tu et al., 2010). Li et al. (2010) also found that low leg IMF content indicates high H-FABP mRNA expression. This phenomenon demonstrates that the relatively high expression of H-FABP mRNA increases fat metabolism and promotes lipolysis to produce more energy and satisfy the requirements of growth, reproduction, and other physiological processes (Li et al., 2010). Guglielmo et al. (2002) noticed the similar occurrence in migratory birds, they clarified that H-FABP mRNA level of chest uscles were highest in the process of migration (10%) and improving H-FABP expression might be carried out by endurance fling training.

CONCLUSION

The G939A site could be taken as genetic marker for higher IMF content selecting for breast muscle of BBOC and leg muscle of WBOC. The IMF content increases and H-FABP gene mRNA abundance decreases with age. The mRNA expression of the H-FABP gene negatively correlates with IMF content in both breast and leg muscles of BOCs.

http://dx.doi.org/10.5713/ajas.14.0886

CONFLICT OF INTEREST

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

ACKNOWLEDGMENTS

This study was supported by the National Natural Science Foundation of China (Project No. 31160521), Tarim University Principal Fund (Project No. TDZKGG201504) and the project of Key Laboratory of Tarim Animal Husbandry Science and Technology, Xinjiang Production & Construction Group (Project No. HS201302).

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Yong Wanga, Jianzhong Hea, Wenxuan Yang (1), Gemenggul Muhantay, Ying Chen, Jinming Xing, and Jianzhu Liu (2) *

College of Animal Science, Key Laboratory of Tarim Animal Husbandry Science and Technology of Xinjiang Production and Construction Groups, Tarim University, Alar, Xinjiang Uygur Autonomous Region 843300, China

* Corresponding Author: Jianzhu Liu. E-mail: liujz@sdau.edu.cn

(1) Inspection Center for the Quality of Agricultural and Sideline Products of Shandong, Zoucheng 273500, China.

(2) College of Veterinary Medicine, Research Center for Animal Disease Control Engineering Shandong, Shandong Agricultural University, Tai'an 271018, China.

(a) These two authors contribute equally to this work.

Submitted Nov. 19, 2014; Revised Feb. 3, 2015; Accepted Mar. 12, 2015

Table 1. H-FABP genotypic frequency and gene frequency of BOCs

Breed            Genotypic frequency (%)

             AA              AB              BB

BBOC     0.15 (9/60)    0.35 (21/60)    0.50 (30/60)
SBOC    0.417 (25/60)   0.366 (22/60)   0.217 (13/60)
WBOC    0.450 (27/60)   0.383 (23/60)   0.167 (10/60)

Breed          Gene frequency (%)

              A                B

BBOC    0.325 (39/120)   0.675 (81/120)
SBOC    0.600 (72/120)   0.400 (48/120)
WBOC    0.642 (77/120)   0.358 (43/120)

H-FABP, heart type fatty acid binding protein; BOCs, Baicheng oil
chickens; BBOC, black Baicheng oil chicken; SBOC, silky Baicheng
oil chicken; WBOC, white Baicheng oil chicken.

AA, AB, and BB were genotypes frequency; A and B were alleles.
They were analyzed by POPGENE software (ver.1.31) according to 60
chickens with with a 1:1 sex ratio of each group.

Table 2. Hereditary character of H-FABP gene of BOCs

Breed    Ho      He      Ne      PIC    [chi square]     p

BBOC    0.442   0.350   1.782   0.343      2.676       0.102
SBOC    0.484   0.367   1.923   0.365      3.593       0.058
WBOC    0.46    0.83    1.851   0.349      1.839       0.175

H-FABP, heart type fatty acid binding protein; BOCs, Baicheng oil
chickens; Ho, observed heterozygosity; He, expected
heterozygosity; Ne, effective number of allele; PIC, polymorphic
information content; BBOC, black Baicheng oil chicken; SBOC,
silky Baicheng oil chicken; WBOC, white Baicheng oil chicken.

Ho, He, Ne, and [x.sup.2] were analyzed by POPGENE software (ver.1.31)
and PIC was analyzed by PowerMaker software (ver.3.25).

Table 3. Relationship between H-FABP gene polymorphism and IMF of
breast muscle

Breed              AA                         AB

BBOC    8.781 [+ or -] 0.575 (a)   6.839 [+ or -] 0.377 (b)
SBOC    6.893 [+ or -] 0.554       5.840 [+ or -] 0.590
WBOC    7.401 [+ or -] 0.498       6.038 [+ or -] 0.539

Breed              BB

BBOC    7.892 [+ or -] 0.315 (ab)
SBOC    6.032 [+ or -] 0.769
WBOC    7.149 [+ or -] 0.818

H-FABP, heart type fatty acid binding protein; IMF, intramuscular
fat; BBOC, black Baicheng oil chicken; SBOC, silky Baicheng oil
chicken; WBOC, white Baicheng oil chicken.

The correlation between H-FABP gene polymorphism and IMF content
was performed by SAS 9.0 using the SAS software PROC GLM
procedures.

(a,b) Means within a row with no common superscript are different
(p < 0.05)

Table 4. Relationship between H-FABP gene polymorphism and IMF of
leg muscle

Breed               AA                          AB

BBOC     13.199 [+ or -] 1.060       11.451 [+ or -] 0.649
SBOC      9.369 [+ or -] 0.995        8.408 [+ or -] 1.061
WBOC    11. 958 [+ or -] 0.636 (a)    9.241 [+ or -] 0.689 (b)

Breed              BB

BBOC    12.004 [+ or -] 0.580
SBOC     9.285 [+ or -] 1.380
WBOC    10.940 [+ or -] 1.05 (ab)

H-FABP, heart type fatty acid binding protein; IMF, intramuscular
fat; BBOC, black Baicheng oil chicken; SBOC, silky Baicheng oil
chicken; WBOC, white Baicheng oil chicken.

The correlation between H-FABP gene polymorphism and IMF content
was performed by SAS 9.0 using the SAS software PROC GLM
procedures.

(a,b) Means within a row with no common superscript are different
(p < 0.05).

Table 5. Correlations between H-FABP abundance and IMF
content in breast muscle and leg muscle of BOCs

                 BBOC     SBOC       BBOC

Breast muscle   -0.219   -0.0.41    -0.074
Leg muscle      -0.212   -0.128    -0.668 *

H-FABP, heart type fatty acid binding protein; IMF, intramuscular
fat; BOCs, Baicheng oil chickens; BBOC, black Baicheng oil
chicken; SBOC, silky Baicheng oil chicken; WBOC, white Baicheng
oil chicken.

The correlation analysis between mRNA expression
([2.sup.-[DELTA]Ct]) and IMF content was assessed by Pearson's
correlation coefficient of SPSS 17.0 at slaughter time,
* p < 0.05.
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Article Details
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Author:Wang, Yong; He, Jianzhong; Yang, Wenxuan; Muhantay, Gemenggul; Chen, Ying; Xing, Jinming; Liu, Jianz
Publication:Asian - Australasian Journal of Animal Sciences
Article Type:Report
Date:Oct 1, 2015
Words:5348
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