南通大学学报(医学版)
南通大學學報(醫學版)
남통대학학보(의학판)
JOURNAL OF NANTONG UNIVERSITY(MEDICAL SCIENCES)
2015年
3期
186-189
,共4页
肌钙蛋白T%可变剪接%心力衰竭%小鼠
肌鈣蛋白T%可變剪接%心力衰竭%小鼠
기개단백T%가변전접%심력쇠갈%소서
cardiac troponin T%alternative splicing%heart failure%mouse
目的:研究肌钙蛋白T(cardiac troponin T, cTnT)基因外显子5(exon 5, E5)的可变剪接及其在真核细胞和小鼠心力衰竭(心衰)模型的表达情况。方法:通过分段PCR构建包含cTnT外显子2~6及相应的内含子的基因片段,连接至真核表达载体中,转染真核细胞HEK293FT,观察其在细胞的表达和在体心肌中的表达是否有异同;建立小鼠心衰模型,用免疫组织化学法和PCR研究cTnT E5的表达情况。结果:cTnT迷你基因在HEK293FT细胞内表达出3个剪接异构体,分别是1个cTnT E5+和2个cTnT E5-;小鼠心脏内主要表达3个剪接异构体,组成情况和迷你基因表达产物相似;小鼠心衰模型组的cTnT E5+比例增高。结论:成功构建cTnT迷你基因,可用于进一步研究cTnT E5的可变剪接表达调控;小鼠心衰模型显示cTnT E5的表达和心肌功能有一定联系。
目的:研究肌鈣蛋白T(cardiac troponin T, cTnT)基因外顯子5(exon 5, E5)的可變剪接及其在真覈細胞和小鼠心力衰竭(心衰)模型的錶達情況。方法:通過分段PCR構建包含cTnT外顯子2~6及相應的內含子的基因片段,連接至真覈錶達載體中,轉染真覈細胞HEK293FT,觀察其在細胞的錶達和在體心肌中的錶達是否有異同;建立小鼠心衰模型,用免疫組織化學法和PCR研究cTnT E5的錶達情況。結果:cTnT迷妳基因在HEK293FT細胞內錶達齣3箇剪接異構體,分彆是1箇cTnT E5+和2箇cTnT E5-;小鼠心髒內主要錶達3箇剪接異構體,組成情況和迷妳基因錶達產物相似;小鼠心衰模型組的cTnT E5+比例增高。結論:成功構建cTnT迷妳基因,可用于進一步研究cTnT E5的可變剪接錶達調控;小鼠心衰模型顯示cTnT E5的錶達和心肌功能有一定聯繫。
목적:연구기개단백T(cardiac troponin T, cTnT)기인외현자5(exon 5, E5)적가변전접급기재진핵세포화소서심력쇠갈(심쇠)모형적표체정황。방법:통과분단PCR구건포함cTnT외현자2~6급상응적내함자적기인편단,련접지진핵표체재체중,전염진핵세포HEK293FT,관찰기재세포적표체화재체심기중적표체시부유이동;건립소서심쇠모형,용면역조직화학법화PCR연구cTnT E5적표체정황。결과:cTnT미니기인재HEK293FT세포내표체출3개전접이구체,분별시1개cTnT E5+화2개cTnT E5-;소서심장내주요표체3개전접이구체,조성정황화미니기인표체산물상사;소서심쇠모형조적cTnT E5+비례증고。결론:성공구건cTnT미니기인,가용우진일보연구cTnT E5적가변전접표체조공;소서심쇠모형현시cTnT E5적표체화심기공능유일정련계。
Objective: To study alternative splicing of cTnT exon 5(E5) in mammalian cells and murine heart failure model.Methods: By segmental PCR strategy, we constructed cTnT mini-gene which consists of its exon 2-6 and the interspersed introns. Then this mini-gene was transfected into HEK293FT cells and then dectected the exon 5 inclusion expression by PCR. Results: We found the cTnT mini-gene expressed three isoforms with one cTnT E5 inclusion band and two cTnT E5 exclusion bands. This was consistent with the expression pattern in murine heart. Moreover, the cTnT E5 inclusion was increased in murine heart failure model compared with that of control group. Conclusion: We successfully constructed a cTnT mini-gene, which is useful for our further study. In addition, dysregulation of cTnT E5 splicing may be responsible for the normal cardiomycyte function.