Gene Expression Patterns in Different Wool Densities of Rex Rabbit Using cDNA Microarray

This study was carried out to identify gene expression patterns in different wool densities of rex rabbit. The mid-dorsal skin samples from 8 rex rabbits were studied. They were divided into two groups according to different wool densities. Total RNA was isolated and labeled by reverse transcription reaction with Cy5-dCTP and Cy3-dCTP for cDNA probe. The cDNA probe was hybridized with cDNA microarrays containing 14 601 rabbit’s genes. The differently expressed genes were analysed with the Gene Ontology （GO） classification and the pathway analysis. Hierarchical clustering was performed to clarify genes in association with different wool densities. The 2 657 differentially expressed genes were identified. Among them, 1 103 genes were functionally known genes, 687 genes were up-regulated and 419 were down-regulated. GO analysis indicated that these altered genes were associated with metabolism, signal transduction, cell cycle, cell adhesion, cell proliferation, cell division, apoptosis, and other processes. KEGG analysis showed that 95 signal pathways associated with up-regulated genes and 87 signal pathways associated with down-regulated genes had changed significantly （P0.05）. Some important differentially expressed genes in different wool densities of rex rabbit were identified, such as MMP2, TGF-β1, TGF-β2, IGF-1, ITGB1, RPS6KB1, BMP2, ActRIIB, CDK2, and CCNA2. Hierarchical clustering analysis separated the differentially expressed genes into 5 main characteristic groups. Data from cDNA microarray experiments clearly distinguished between group A and group B. Some important genes were identified, which might be useful in further study on wool density markers of rex rabbit.

Differential Expression of CCNA2 Gene and MMP2 Gene in Skin Tissue of Rex Rabbit with Different Fur Densities

[ Objective] The paper was to search for the molecular marker highly associated with fur density of rex rabbit. [ Method ] Experimental rex rabbits were divided into dense fur group and sparse fur group. The variation rule of gene expression in skin tissue of rex rabbits with different fur densities was detected using rabbit whole gene cDNA microarray. [ Result] A total of 2 657 genes with differential expression were detected by microarray test, including 1 106 genes with known function, 687 genes with up-regulated expression and 419 genes with down-regulated expression. The expression levels of multiple genes involving in cell proliferation, differentiation, apoptosis and migration had significant changes. MMP2 gene had high expression in skin tissue of rex rabbits in dense fur group, which was 8. 195 times of gene expression in sparse fur group ; CCNA2 gene had low expression in skin tissue of rex rabbit in dense fur group, which was 0. 143 times of gene expression in spaarse fur group. [ Conclusion ] The results provide the theoretical basis and research direction for early breeding of rex rabbit in practical production.

Effects of Different Feed Additives on Fur Production Performance of Rex Rabbit

[ Objectivel To investigate the effects of three different levels of feed additives on fur production performance of Rex rabbit. [ Method] A total of 60 healthy American strain Rex rabbits at the age of 60 d （female：male =1：1 ） were randomly divided into group I, group II and group III. The Rex rabbits in the group I were fed basal diet containing nutritional substances; those in the group II were fed basal diet containing nutdtionai substances and Chinese herbal additive; and those in the group III were fed basal diet containing nutritional substances, Chinese herbal additive and enzyme. The trial lasted for 100 d. After slaughtering, the fur area, fur thickness, wool density, wool fineness and coarse wool rate were determined. [Result] The fur production performance of group III was significantly higher than that of group I （ P 〈 0.05）. There was no significant difference between group III and group II. [ Conclusion] Supplementing Chinese herbal additive and enzyme in diet can improve the fur production performance of Rex rabbit.

Genetic and epigenetic targets of natural dietary compounds as anti-Alzheimer's agents

Alzheimer’s disease is a progressive neurodegenerative disorder and the most common cause of dementia that principally affects older adults.Pathogenic factors,such as oxidative stress,an increase in acetylcholinesterase activity,mitochondrial dysfunction,genotoxicity,and neuroinflammation are present in this syndrome,which leads to neurodegeneration.Neurodegenerative pathologies such as Alzheimer’s disease are considered late-onset diseases caused by the complex combination of genetic,epigenetic,and environmental factors.There are two main types of Alzheimer’s disease,known as familial Alzheimer’s disease(onset<65 years)and late-onset or sporadic Alzheimer’s disease(onset≥65 years).Patients with familial Alzheimer’s disease inherit the disease due to rare mutations on the amyloid precursor protein(APP),presenilin 1 and 2(PSEN1 and PSEN2)genes in an autosomaldominantly fashion with closely 100%penetrance.In contrast,a different picture seems to emerge for sporadic Alzheimer’s disease,which exhibits numerous non-Mendelian anomalies suggesting an epigenetic component in its etiology.Importantly,the fundamental pathophysiological mechanisms driving Alzheimer’s disease are interfaced with epigenetic dysregulation.However,the dynamic nature of epigenetics seems to open up new avenues and hope in regenerative neurogenesis to improve brain repair in Alzheimer’s disease or following injury or stroke in humans.In recent years,there has been an increase in interest in using natural products for the treatment of neurodegenerative illnesses such as Alzheimer’s disease.Through epigenetic mechanisms,such as DNA methylation,non-coding RNAs,histone modification,and chromatin conformation regulation,natural compounds appear to exert neuroprotective effects.While we do not purport to cover every in this work,we do attempt to illustrate how various phytochemical compounds regulate the epigenetic effects of a few Alzheimer’s disease-related genes.

Form Gene Clustering Method about Pan-Ethnic-Group Products Based on Emotional Semantic

The use of pan-ethnic-group products form knowledge primarily depends on a designer＇s subjective experience without user participation. The majority of studies primarily focus on the detection of the perceptual demands of consumers from the target product category. A pan-ethnic-group products form gene clustering method based on emotional semantic is constructed. Consumers＇ perceptual images of the pan-ethnic-group products are obtained by means of product form gene extraction and coding and computer aided product form clustering technology. A case of form gene clustering about the typical pan-ethnic-group products is investigated which indicates that the method is feasible. This paper opens up a new direction for the future development of product form design which improves the agility of product design process in the era of Industry 4.0.

Association of vascular endothelial growth factor-634G/C and receptor for advanced glycation end products G82S gene polymorphisms with diabetic retinopathy

AIMTo investigate the association of receptor for advanced glycation end products (RAGE) G82S and vascular endothelial growth factor (VEGF) -634 G/C gene polymorphisms with diabetic retinopathy (DR).METHODSOur cross-sectional study included 61 diabetic patients, 12 of them had proliferative diabetic retinopathy (PDR), 15 had non proliferative diabetic retinopathy (NPDR), 34 had no diabetic retinopathy (NDR) and 61 healthy controls. Participants were tested for RAGE G82S and VEGF -634 G/C polymorphisms by polymerase chain reaction-restriction fragment length polymorphism.RESULTSWe found a significant association between VEGF -634 G/C polymorphism and PDR as PDR patients had increased incidence of VEGF -634 CC genotype compared to NDR patients [odds ratio for CC vs (GC+GG)=6.5, 95% CI=1.5-27.8, P=0.021]. Also VEGF -634 CC genotype and C allele were significantly higher in the PDR than in NPDR patients, which is a novel finding in our study (P=0.024, 0.009 respectively). The mean triglycerides level was significantly higher in diabetic patients with CC genotype (P=0.01) as compared to patients with other genotypes. All cases and control subjects were of the same heterozygous RAGE 82G/S genotype.CONCLUSIONPatients carrying VEGF -634 C polymorphism have a higher risk of PDR development, so VEGF -634 G/C polymorphism could be used as a predictive marker for PDR in diabetic patients. We could not find a significant association between RAGE G82S polymorphism and DR.

自抗性基因导向的活性天然产物挖掘

天然产物是医药与农药的重要来源。基因组测序和生物信息学分析技术的飞速发展,揭示了大量功能未知的天然产物生物合成基因簇,利用生物信息学工具,从这些庞大的基因簇数据中挖掘活性天然产物已经成为发现新型天然药物的重要途径。天然产物的生产者们利用自抗性基因所表达的自抗性酶来保护自身,这种自抗性酶是体内一些初级代谢途径中管家酶的变体,不但对于活性天然产物具有较好的耐受性,还可以在生产活性天然产物的同时确保宿主体内代谢的正常进行。因而,自抗性基因指导的天然产物研究有效地将活性导向和基因组导向的天然产物发掘策略桥连起来,为精准发掘具有目标活性的新型天然产物提供了有效策略。本文对利用自抗性基因作为探针进行天然产物发掘的代表性研究工作进行了整理和总结,并对研究趋势进行了展望,主要包括:①对于活性已知的天然产物,利用其自抗性基因来定位生物合成基因簇的研究;②以天然产物生物合成基因簇中的自抗性基因为线索,预测产物的作用靶点的研究;③利用天然产物自抗性机制,将具有已知作用机制的活性分子进行快速排重的研究;④利用自抗性基因与天然产物及其活性的内在联系,以目标靶点导向的活性天然产物基因组挖掘;⑤自抗性基因导向的基因组数据挖掘工具的发展情况。

南粳系列超级稻品种灌浆期光合产物的分配特性

【目的】研究南粳系列超级稻灌浆期光合产物转运和分配及相关基因表达量的变化特性及其与对照品种的差异,总结南粳系列超级稻高产的生理优势,为优质高产粳稻的培育提供理论依据。【方法】采用南粳5718、南粳晶谷、南粳3908和南粳5055为研究对象,以淮稻5号为对照,在孕穗期、开花期以及开花后每隔7 d至成熟期测定剑叶光合速率、地上部干物质分配和转运,以及剑叶和籽粒发育不同时期物质转运相关基因的表达量,统计产量差异。【结果】南粳系列超级稻产量和千粒重高于淮稻5号,其剑叶净光合速率在孕穗期和花后28 d显著高于淮稻5号。在物质转运方面,南粳系列超级稻开花后茎叶干重、叶片输出量、输出率和转运率显著高于淮稻5号,其中南粳5718叶片输出量和输出率最高。南粳5718剑叶中与淀粉降解和糖类代谢相关基因(OsSPS1,OsSUT2,OsGWD1)的表达比其他品种启动早,最高表达量也高于其他品种。籽粒中SWEET基因在灌浆早期的蔗糖转运过程中扮演重要角色,中后期OsPK3、OsSUT1、OsSUT2基因在糖类的运输卸载中发挥重要作用,OsAGPL2和OsDPE1基因在中后期淀粉合成中发挥重要作用,南粳5718、南粳晶谷、南粳3908籽粒中与淀粉合成和糖类运输的相关基因在不同时期的表达量显著高于淮稻5号。【结论】南粳系列超级稻较高的产量在物质转运方面主要有以下特征:茎秆和叶片物质积累量多,穗积累量大,叶片和茎秆物质转运率高;叶片中蔗糖代谢和转运相关基因表达量高,有利于蔗糖在源端的合成、装载和转运;籽粒中蔗糖转运和淀粉合成相关基因表达量高,有利于蔗糖在库端的卸载及籽粒中淀粉的合成。

杜撒×大长撒VRTN基因多态及其与生产性状的关联研究

为研究杜撒×大长撒VRTN基因多态及其对育肥、胴体、肉质的影响。采用PCR直接测序法对杜撒×大长撒、杜洛克、长白、大白VRTN基因启动子区和4个外显子区进行单核苷酸多态性检测,计算VRTN基因多态位点基因型频率及基因频率,测定杜撒×大长撒猪群的育肥、胴体和肌肉品质,采用最小二乘模型分析VRTN基因与育肥、胴体、肉质的关联。结果显示:在4个猪群中共检测到VRTN g.97615896_97615897ins291和VRTN g.97622607G>A 2个突变位点具有多态性,其中,g.97615896_97615897ins291在4个猪群中均存在Q/Q、Q/Wt、Wt/Wt 3种基因型,4个群体均属于中度多态,均处于Hardy-Weinberg平衡状态;杜撒×大长撒g.97615896_97615897ins291位点Q/Q基因型活体背膘厚比Wt/Wt基因型少0.36 mm(P<0.05)、肋骨数比Wt/Wt基因型多0.63对(P<0.01),Q/Wt基因型胴体斜长比Wt/Wt长1.56 cm(P<0.05),Q/Q和Q/Wt基因型眼肌面积比Wt/Wt多4.38 cm^(2)、4.34 cm^(2)(P<0.05),Q/Q基因型瘦肉率比Wt/Wt高3.23百分点(P<0.05)、脂率比Wt/Wt低4.1百分点(P<0.05);VRTN g.97622607G>A位点在杜撒×大长撒属于低度多态(PIC=0.0799),处于Hardy-Weinberg平衡状态;杜撒×大长撒VRTN g.97622607G>A位点GG基因型30~100 kg日增重比GA基因型多61.43 g·d^(-1)(P<0.01),瘦肉率比GA基因型高2.53百分点(P<0.05)。结果表明:VRTN g.97615896_97615897ins291位点插入等位基因Q可增加杜撒×大长撒猪群肋骨数、胴体斜长、眼肌面积和瘦肉率,降低活体背膘厚和脂率;VRTN g.97622607G>A位点GG基因型可提高杜撒×大长撒猪群的日增重和瘦肉率。本研究结果为利用VRTN基因进行分子标记辅助选择提高撒坝猪的生产性能提供依据。

文化基因视域下区域农产品品牌视觉形象设计

随着国家对乡村振兴事业的进一步扶持,区域农产品品牌化已成为必然趋势。针对现阶段区域农产品品牌视觉形象良莠不齐、同质化严重的现状,探索文化基因视域下区域农产品品牌视觉形象的设计原则与设计策略,旨在通过地域文化赋能品牌的方式打造差异化定位,为其创意设计及其延展提供源源不断的设计动力;层次分析法的介入可以通过为创意设计提供量化依据,来克服传统方案在择优过程中的绝对主观性,从而减少品牌的试错成本。

深加工益生菌产品中常用7种乳杆菌的快速鉴定

目的探讨适用于复杂基质中益生菌产品的DNA提取方法,并通过鉴定7种常见的乳杆菌,比较产品标签标示与实际添加乳杆菌种类的一致性。方法本研究采用了3种不同的DNA提取方法,分别为十六烷基三甲基溴化铵(cetyltrimethylammonium bromide,CTAB)法、磁珠法深加工产品基因组DNA抽提试剂盒(磁珠法)和Ezup柱式深加工产品基因组DNA抽提试剂盒(柱式法);通过测定DNA浓度、纯度以及利用16SrDNA V3/V4基因扩增技术评估DNA质量。此外合成嗜酸乳杆菌、德氏乳杆菌保加利亚亚种、罗伊氏粘液乳杆菌、植物乳植杆菌、干酪乳酪杆菌、鼠李糖乳酪杆菌和副干酪乳酪杆菌特异性引物探针,利用实时荧光定量聚合酶链式反应(real-time fluorescence quantitative PCR,qPCR)技术验证方法的特异性、灵敏度和重复性,进一步对市售益生菌产品进行乳杆菌种类的鉴定。结果综合3个DNA质量评价方法,使用CTAB法提取的DNA质量较高,纯度在1.7~2.1之间,质量浓度大于25ng/mL,且16SrDNAV3/V4基因扩增的循环数阈值(cycle threshold,Ct)值均小于35,符合后续qPCR扩增要求;相比之下,柱式法除了饼干类产品DNA纯度为1.96±0.13,浓度为79.07±2.15,扩增Ct值为22.67±3.09能够达到要求外,提取的其他产品DNA和磁珠法提取的DNA无法同时满足3个DNA评价方法要求且重复性较差。本研究所使用的引物和探针对目标乳杆菌有明显的特异性扩增,灵敏度范围为0.0100~1.0000ng/μL和10^(3)~10^(4)CFU/mL,且重复性良好[相对标准偏差(relative standard deviation,RSD)≤3.02%]。检测的20批市售产品中,6批产品未检出标示的乳杆菌种类,存在标示与实际检出菌种不符的情况。结论CTAB法因其较高的适应性和低成本,在提取复杂基质中益生菌产品的DNA时表现更优,结合qPCR方法能有效实现产品中乳杆菌种水平鉴定;然而针对干酪乳酪杆菌的检出限需要进一步研究开发更为灵敏的引物和探针。

基于眼动追踪的产品族设计基因识别强度研究

目的对小米品牌产品族中多品类的产品设计开展案例研究,探索其设计基因的构成特性,研究分析产品设计基因的识别强度差异性,进而初步形成产品设计基因的提取及构建方法,以及识别强度分析方法。方法首先构建产品设计基因识别强度对比方法,通过卡片分类法、聚类分析法和多维尺度分析法筛选出典型样本;其次由问卷分析和设计形态分析提取典型基因;最后结合眼动追踪和熵权法综合评价基因识别强度差异。结果形成小米品牌产品(家电与智能类)因子库,包含通用型基因5项,专用型基因18项,且通用型基因的识别强度高于专用型基因。结论初步构建了基于眼动追踪的产品族设计基因识别强度研究方法,可以此作为基础规划及管理产品设计方案,使产品设计兼顾品牌基因的延续性及单品设计的合理性;同时还可为生态链企业研发同品牌、不同品类产品提供设计策略与参考。

济南市食品和腹泻病人来源副溶血性弧菌分子分型及毒力基因分析

目的:了解济南市动物性海产品、腹泻患者来源副溶血性弧菌的脉冲场凝胶电泳分子分型特征以及菌株携带毒力基因的情况。方法:按照《国家食品污染和有害因素风险监测工作手册》的方法采集动物性海产品150份,依据《山东省食源性疾病主动监测工作手册》采集腹泻病人样本771份,对上述两类样本进行副溶血性弧菌分离。用脉冲场凝胶电泳对129株副溶血性弧菌进行分子分型和聚类分析,利用多重荧光PCR检测菌株毒力基因的携带情况。结果:动物性海产品来源副溶血性弧菌的总检出率为41.3%,腹泻病人副溶血性弧菌的检出率为6.1%~14.2%。动物性海产品和腹泻患者来源的129株副溶血弧菌可分为93个脉冲场凝胶电泳型别,相似性系数为35.1%~100.0%。患者来源的菌株带型相似系数高于85.0%的占比为90.4%,89.3%动物性海水产品来源的菌株带型相似系数低于85.0%。73株患者来源的菌株携带tdh基因的菌株占比为95.9%,携带trh基因的菌株占比为6.8%,4.1%的菌株同时携带两个毒力基因。动物性海产品来源的56株菌均不携带毒力基因tdh,携带耐热相关溶血素的菌株占比为3.6%。结论:两种来源的菌株在分子分型和毒力基因携带方面存在差异,动物性海产品携带副溶血性弧菌的比例较高,有必要进一步加强对动物性海产品副溶血性弧菌的监测,扩大采样量并增加菌落挑取数量以进一步明确该菌株的传播、流行特征,为制定防控策略提供科学依据。

三生空间视角下传统村落空间基因图谱构建及特征解析——以扎尕那村为例

传统村落三生空间的优化布局有赖于对其空间特征及其内在结构的认识。文章以扎尕那村为例,从三生空间的视角建立空间基因图谱,并以此为基础确定村落三生空间基因特征。研究表明:(1)基于土地利用数据构建三生空间基因描述具有区别于单一空间基因的新维度;(2)运用参数化方法进行空间基因识别提取具有可操作性;(3)借助“三生空间关系”图形及“地理信息要素分类”编码的形式实现空间基因图谱表达可更好服务于国土空间规划;(4)基于空间基因图谱识别出的扎尕那三生空间特征明显,生态空间由9种景观类型组成,裸岩与林地是景观的基质;生活空间建设用地破碎度较高,呈自由式带状布局;生产空间形成农林牧垂直经济类型。

湘赣边区红色文化创意产品的适应性开发与设计

设计赋能文化传承的背景下,文化创意产品地域文化转译的同质化、传播力的疲软化制约了文化传承。本研究以湘赣边区红色文化创意产品设计为例,提出文化创意产品适应性开发方法,即凸显湘赣边区的红色文化,精准文化转译;匹配红色旅游群体的差异化需求,提升文化传播力。首先,以大学生群体为研究对象,依据用户消费类别偏好量表和产品需求特征量表探测用户需求。然后,解析湘赣边区红色文化基因,指导产品设计实践。最后,从设计层、功能层、文化层对设计产品展开后期评估,实证文化创意产品适应性开发方法的可行性。研究结果表明,湘赣边区红色文化创意产品的适应性开发方法能够辅助设计师的设计决策。

基于黄河文化基因解码的文化创意产品设计研究

为了弘扬中华优秀传统文化,提升文化基因在文创产品设计中的应用,文章通过Cite Space和SPSS工具对黄河地域文化的历史渊源和发展脉络进行基因解码探究。依据文化基因理论,将黄河文化解码为自然地理文化基因、民俗风情文化基因和历史积淀文化基因,提出了黄河文化基因解码视域下的文创产品设计思路,并从基因解码视角对黄河地域文创产品进行设计。文章将文化基因解码理念融入设计实践,为促进文化传承与地域文创产业的发展提供新的思路。

长沙地域文化在文创产品设计中的应用研究

本文以长沙的地域文化基因为切入点,对其在文创产品设计中的应用进行研究,探索具有独特文化特征与城市魅力的文创产品,通过借用生物学中的遗产基因概念,推理出长沙地域文化基因图谱,将长沙地域文化基因融入文创产品设计中,彰显长沙地域文化的鲜明特色,同时带动地域文化产业的蓬勃发展,促进长沙地域文化创意产业的繁荣,希望所提出的设计思路能为其他地域文创产品的创新设计提供有价值的借鉴与方向。

沙发产品形态基因及遗传力分析

在企业沙发产品研发中,每一代沙发产品之间基本上都具有一定的连贯性和继承性,延续着沙发产品族的特征。论文以某品牌沙发产品中四组主要款式为主,提取最有遗传力的形态基因,完善其产品族构筑。运用形态分析法提取显性形态特征,提取过程中采用标准差系数算法,以反映各个特征间的差异性,对性状较强的形态特征的遗传力做判断,标准差系数越小,遗传力越强,从而确定最具遗传力的显性形态基因。经遗传力的分析,得到沙发产品中最具遗传力的5个形态基因:贵妃位扶手长短与贵妃位之间的形式、贵妃位边沿、扶手与座基架间的连接形式、扶手和靠背架之间的位置形式、整体轮廓线。这些可以被传承的形态基因有利于沙发产品族的构建,也为设计师进行产品迭代设计提供了重要参考。

我国先进治疗药品的范围及分类研究和建议

近年来先进治疗药品研发申报呈爆发式增长,引领生物医药的第三次产业革命。全球范围内嵌合抗原受体T细胞(CAR-T)治疗产品、腺相关病毒载体基因治疗产品等不同类型的细胞和基因治疗产品相继批准上市,为复发难治疾病提供了有效的治疗手段。先进治疗药品通常采用细胞或组织经基因修饰和(或)体外操作制备,种类包括基因修饰细胞、核酸、病毒载体和人工组织等。由于这类产品类型复杂、多样,明确其定义和分类,有利于优化产品注册申报路径,加速各类产品技术指南的发布,推动产品快速研发上市,助力我国药品监管与国际接轨。本文通过调研美国食品药品监督管理局(FDA)、欧洲药品管理局(EMA)、日本药品医疗器械综合机构(PMDA)等药品监管机构在法规层面对先进治疗药品的定义及监管分类情况,结合我国产品申报现状和审评积累,提出了对先进治疗药品分类和描述的建议,为我国相关监管政策制定提供参考。

Identification of SNPs in Bovine SLC27A1 Gene and Its Effects on Milk Production Traits in Chinese Holstein Cattle

[Objective] This study discussed the SNPs of SLC27A1 gene and its relationship with milk production traits in Chinese Holstein Cattle in order to find the SNP site which had significant effect on milk production traits in Chinese Holstein Cattle.[Method] DNA was extracted from the bleed of 48 Chinese Holstein Cattle selected according to phenotypic character and mixed into DNA pool for SNPs detection by polymerase chain reaction-single strand conformation polymorphism（PCR-SSCP）and cloning sequencing.Then different genotypes were detected in other 231 Chinese Holstein Cattle by PCR-RFLP.The association between genotype and production traits was assessed by GLM procedure,SAS version 8.02.[Result] There were T112C in exon3 and G64A loci in 3＇UTR,among them the T112C in exon3 was synonymous mutation.There were 3 genotypes TT,TC and CC in T112C locus and 3 genotypes GG,GA and AA in G64A locus.The population was at Hardy-Weinberg equilibration.Cows with genotype CC had significantly highest milk yield than those with genotype TC（P0.01）,and there were no significant differences among the 3 genotypes on milk protein percent and milk fat percent（P0.05）,but the tendency of CC TC TT on milk protein percent and the tendency of TT TC CC on milk fat percent were showed.There was no significant difference among the 3 genotypes of G64A loci on milk yield,milk protein percent and milk fat percent（P0.05）,but the tendency of GA GG AA on milk yield and the tendency of AA GG GA both on milk protein percent and milk fat percent were showed.[Conclusion] There was certain relation between the T112C locus and milk yield traits;It may improve milk yield to raise the frequency of genotype CC;SLC27A1 gene could be a useful candidate gene in selection program on milk yield traits in Chinese Holstein Cattle,which provided a theoretical basis for the marker-assisted breeding and further study of SLC27A1 gene.