Cameron H S, Szczepaniak D, Weston B W
Department of Pediatrics, University of North Carolina at Chapel Hill 27599-7220, USA.
J Biol Chem. 1995 Aug 25;270(34):20112-22. doi: 10.1074/jbc.270.34.20112.
The human alpha(1,3)-fucosyltransferase genes FUT3, FUT5, and FUT6 form a cluster on chromosome 19p13.3. Expression was studied using reverse transcriptase-polymerase chain reaction, rapid amplification of cDNA ends, and Northern analyses. FUT3 and FUT6 were expressed at high levels, while FUT5 expression was lower and restricted to fewer cell types. Alternatively spliced transcripts were identified for FUT3 and FUT6 in kidney, liver, and colon. A 2.37-kilobase pair (kb) FUT3 transcript, detected at high levels in kidney and colon, was absent in liver. FUT6 expression was characterized by a 3.5-kb transcript present in kidney and liver, and a 2.5-kb transcript in colon and liver. Two polyadenylation sites were shown for FUT5, but absence of consensus sequences suggests reduced efficiency for cleavage and polyadenylation. Two polyadenylation sites were also shown for FUT6, with the alternatively spliced downstream signal in tissues expressing high levels of FUT6. In these tissues, additional splicing results in isoforms with catalytic domain deletions. No detectable alpha(1,3)- or alpha(1,4)-fucosyltransferase activity was found in assays of cells transfected with FUT6 isoform cDNAs. Thus, tissue-specific post-transcriptional modifications are associated with expression patterns of FUT3, FUT5, and FUT6.
人类α(1,3)-岩藻糖基转移酶基因FUT3、FUT5和FUT6在19号染色体p13.3上形成一个基因簇。使用逆转录聚合酶链反应、cDNA末端快速扩增和Northern分析研究了其表达情况。FUT3和FUT6高水平表达,而FUT5表达较低且局限于较少的细胞类型。在肾、肝和结肠中鉴定出FUT3和FUT6的可变剪接转录本。在肾和结肠中高水平检测到的2.37千碱基对(kb)FUT3转录本在肝脏中不存在。FUT6表达的特征是在肾和肝中存在一个3.5 kb的转录本,在结肠和肝中存在一个2.5 kb的转录本。FUT5显示有两个聚腺苷酸化位点,但缺乏共有序列表明其切割和聚腺苷酸化效率降低。FUT6也显示有两个聚腺苷酸化位点,在表达高水平FUT6的组织中有可变剪接的下游信号。在这些组织中,额外的剪接导致具有催化结构域缺失的异构体。在用FUT6异构体cDNA转染的细胞检测中未发现可检测到的α(1,3)-或α(1,4)-岩藻糖基转移酶活性。因此,组织特异性转录后修饰与FUT3、FUT5和FUT6的表达模式相关。