Ueki K, Ramaswamy S, Billings S J, Mohrenweiser H W, Louis D N
Department of Pathology (Neuropathology), Massachusetts General Hospital, Charlestown 02129, USA.
Somat Cell Mol Genet. 1997 May;23(3):229-31. doi: 10.1007/BF02721375.
Exon trapping from cosmids mapping to chromosome 19q13.3 yielded 6 exonic sequences that matched the human symplekin gene, which encodes a tight junction-related protein. One exonic sequence identified a 4.0 kb brain cDNA clone, R6E1, which contained 302 bp 5' to the originally reported 3.7 kb symplekin cDNA. A portion of this novel 5' sequence matched an additional trapped exonic sequence which was obtained from the most telomeric cosmid analyzed. The symplekin gene thus lies in a telomeric-to-centromeric direction on 19q13.3. Only three cosmids from a large 19q13.3 contig hybridized with R6E1, thereby assigning the symplekin gene to a 40 kb region immediately telomeric to gene 59 and the DM protein kinase gene. The 5' end of the R6E1 clone has a potential initiation codon with a strong Kozak sequence and Northern blot analysis detected a 4.2 kb signal in most human tissues, indicating that R6E1 may be a complete cDNA sequence. Based on the trapped exonic sequences, twelve exon-intron boundaries were predicted.
从定位于19号染色体19q13.3的黏粒中进行外显子捕获,得到了6个与人类共生蛋白基因匹配的外显子序列,该基因编码一种紧密连接相关蛋白。一个外显子序列鉴定出一个4.0kb的脑cDNA克隆R6E1,它在最初报道的3.7kb共生蛋白cDNA的5'端含有302bp。这个新的5'序列的一部分与另一个从分析的最末端黏粒中获得的捕获外显子序列匹配。因此,共生蛋白基因在19q13.3上呈从端粒到着丝粒的方向排列。在一个大的19q13.3重叠群中,只有3个黏粒与R6E1杂交,从而将共生蛋白基因定位到基因59和DM蛋白激酶基因紧邻端粒的一个40kb区域。R6E1克隆的5'端有一个带有强科扎克序列的潜在起始密码子,Northern印迹分析在大多数人类组织中检测到一个4.2kb的信号,表明R6E1可能是一个完整的cDNA序列。基于捕获的外显子序列,预测了12个外显子-内含子边界。