Claffey K P, Herrera V L, Brecher P, Ruiz-Opazo N
Department of Biochemistry, Boston University School of Medicine, Massachusetts 02118.
Biochemistry. 1987 Dec 1;26(24):7900-4. doi: 10.1021/bi00398a054.
A fatty acid binding protein (FABP) has been identified and characterized in rat heart, but the function and regulation of this protein are unclear. In this study the cDNA for rat heart FABP was cloned from a lambda gt11 library. Sequencing of the cDNA showed an open reading frame coding for a protein with 133 amino acids and a calculated size of 14776 daltons. Several differences were found between the sequence determined from the cDNA and that reported previously by protein sequencing techniques. Northern blot analysis using rat heart FABP cDNA as a probe established the presence of an abundant mRNA in rat heart about 0.85 kilobases in length. This mRNA was detected, but was not abundant, in fetal heart tissue. Tissue distribution studies showed a similar mRNA species in red, but not white, skeletal muscle. In general, the mRNA tissue distribution was similar to that of the protein detected by Western immunoblot analysis, suggesting that heart FABP expression may be regulated at the transcriptional level. S1 nuclease mapping studies confirmed that the mRNA hybridized to rat heart FABP cDNA was identical in heart and red skeletal muscle throughout the entire open reading frame. The structural differences between heart FABP and other members of this multigene family may be related to the functional requirements of oxidative muscle for fatty acids as a fuel source.
在大鼠心脏中已鉴定并表征了一种脂肪酸结合蛋白(FABP),但该蛋白的功能和调节尚不清楚。在本研究中,从λgt11文库中克隆了大鼠心脏FABP的cDNA。对该cDNA进行测序显示,其开放阅读框编码一种含有133个氨基酸、计算分子量为14776道尔顿的蛋白质。通过cDNA确定的序列与先前通过蛋白质测序技术报道的序列存在一些差异。以大鼠心脏FABP cDNA为探针进行的Northern印迹分析表明,大鼠心脏中存在一种丰富的mRNA,长度约为0.85千碱基。在胎儿心脏组织中检测到了这种mRNA,但不丰富。组织分布研究表明,在红色而非白色骨骼肌中存在类似的mRNA种类。总体而言,mRNA的组织分布与Western免疫印迹分析检测到的蛋白质分布相似,这表明心脏FABP的表达可能在转录水平受到调节。S1核酸酶图谱分析证实,与大鼠心脏FABP cDNA杂交的mRNA在心脏和红色骨骼肌的整个开放阅读框中是相同的。心脏FABP与该多基因家族其他成员之间的结构差异可能与氧化型肌肉对脂肪酸作为燃料来源的功能需求有关。