遗传
遺傳
유전
Hereditas
2015年
9期
926-931
,共6页
李利族%韩丽鑫%王金奎%汪亮%刘娣%杨秀芹
李利族%韓麗鑫%王金奎%汪亮%劉娣%楊秀芹
리리족%한려흠%왕금규%왕량%류제%양수근
猪%PILRA%克隆%表达
豬%PILRA%剋隆%錶達
저%PILRA%극륭%표체
porcine%PILRA%cloning%expression
Ⅱ型成对免疫球蛋白样受体(Paired immunoglobulin-like type 2 receptors, PILRs)是免疫球蛋白超家族成员之一,包括α和β两个亚型。PILRα在机体抵抗病原体入侵的免疫反应中发挥着重要作用,但目前尚未见关于猪PILRα的报道。为了分析其在猪抗病育种中的作用,本文克隆了猪PILRα编码基因(PILRA)并鉴定变异剪接体,利用实时荧光定量PCR方法构建其组织表达谱和诱导表达谱。结果表明,成功克隆了猪 PILRA基因的3个变异剪接体V1~V3(GenBank登录号:KJ143679~81),预测的蛋白质多肽链分别长271 aa、254 aa和283 aa,且都具有免疫球蛋白结构域。各变异剪接体均在脾脏中表达量最高,肝脏、肺脏次之,在心脏、肾脏、胃、肌肉、淋巴、大肠、小肠和膀胱等组织中表达量较低或检测不到。Poly(I:C)能显著诱导变异剪接体 V1的表达,但几乎不影响V2、V3的表达。研究结果为进一步揭示PILRA在猪抗病育种中的作用提供了基础。
Ⅱ型成對免疫毬蛋白樣受體(Paired immunoglobulin-like type 2 receptors, PILRs)是免疫毬蛋白超傢族成員之一,包括α和β兩箇亞型。PILRα在機體牴抗病原體入侵的免疫反應中髮揮著重要作用,但目前尚未見關于豬PILRα的報道。為瞭分析其在豬抗病育種中的作用,本文剋隆瞭豬PILRα編碼基因(PILRA)併鑒定變異剪接體,利用實時熒光定量PCR方法構建其組織錶達譜和誘導錶達譜。結果錶明,成功剋隆瞭豬 PILRA基因的3箇變異剪接體V1~V3(GenBank登錄號:KJ143679~81),預測的蛋白質多肽鏈分彆長271 aa、254 aa和283 aa,且都具有免疫毬蛋白結構域。各變異剪接體均在脾髒中錶達量最高,肝髒、肺髒次之,在心髒、腎髒、胃、肌肉、淋巴、大腸、小腸和膀胱等組織中錶達量較低或檢測不到。Poly(I:C)能顯著誘導變異剪接體 V1的錶達,但幾乎不影響V2、V3的錶達。研究結果為進一步揭示PILRA在豬抗病育種中的作用提供瞭基礎。
Ⅱ형성대면역구단백양수체(Paired immunoglobulin-like type 2 receptors, PILRs)시면역구단백초가족성원지일,포괄α화β량개아형。PILRα재궤체저항병원체입침적면역반응중발휘착중요작용,단목전상미견관우저PILRα적보도。위료분석기재저항병육충중적작용,본문극륭료저PILRα편마기인(PILRA)병감정변이전접체,이용실시형광정량PCR방법구건기조직표체보화유도표체보。결과표명,성공극륭료저 PILRA기인적3개변이전접체V1~V3(GenBank등록호:KJ143679~81),예측적단백질다태련분별장271 aa、254 aa화283 aa,차도구유면역구단백결구역。각변이전접체균재비장중표체량최고,간장、폐장차지,재심장、신장、위、기육、림파、대장、소장화방광등조직중표체량교저혹검측불도。Poly(I:C)능현저유도변이전접체 V1적표체,단궤호불영향V2、V3적표체。연구결과위진일보게시PILRA재저항병육충중적작용제공료기출。
Paired immunoglobulin-like type 2 receptors (PILRs) are members of the immunoglobulin superfamily and composed of two subtypes, α and β.PILRα plays an important role in the immune response against invading pathogens, but so far there is no report on porcinePILRα. In order to analyze the potential role of PILRα in porcine disease-resistant breeding, we first cloned thePILRA gene (V1-V3, GenBank accession Nos. KJ143679-81) into pigs, and identified its three splice variants. Each variant conceptually translates into proteins of 271 amino acids (aa), 254aa and 283aa, respectively. Furthermore, quantitative real-time PCR was used to construct expression profiles of each variant in tissues and that induced by Poly(I:C). All three variants had the highest expression levels in the spleen, followed by liver and lung tissues. While levels were low or undetectable in the heart, kidney, stomach, muscle, lymph, large intestine, small intestine and bladder. Poly(I:C) significantly induced the expression of splice variant 1 (V1) of porcinePILRA, but hardly affected the expression of V2 and V3. The results lay a foundation for further study on the role ofPILRA in porcine breeding and disease resistance.