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缺乏ABL外显子a2的BCR/ABL转录本病例中ABL基因断点的异质性

Heterogeneity of the breakpoint in the ABL gene in cases with BCR/ABL transcript lacking ABL exon a2.

作者信息

Iwata S, Mizutani S, Nakazawa S, Yata J

机构信息

Department of Pediatrics, Tokyo Medical and Dental University, Japan.

出版信息

Leukemia. 1994 Oct;8(10):1696-702.

PMID:7934165
Abstract

We report cases with a variant BCR/ABL mRNA expression lacking ABL exon a2 sequences. Two of these cases showed major breakpoint cluster region (BCR) exon 3 (b3) and ABL exon 3 (a3) junction (b3/a3), while the other case showed minor BCR exon 1 (e1) and a3 junction (e1/a3). One of the two cases with b3/a3 junction and the case with e1/a3 junction were diagnosed as acute lymphoblastic leukemia, and the remaining case with b3/a3 junction was chronic myeloid leukemia. Two of these cases, however, were found to have a breakpoint in the ABL gene outside of the intron between exons a2 and a3, probably 5' upstream of exon a2, suggesting that the BCR exon was spliced to ABL exon a3. These findings differ from those previously reported, in which the breakpoints in the ABL gene were between exons a2 and a3, and indicate a novel mechanism for the deletion of ABL exon a2 sequences in the formation of a variant BCR/ABL fusion transcript. The significance of the finding that a part of the SH3 region of ABL protein is missing in some Philadelphia chromosome-positive leukemias is discussed in reference to the cases reported previously.

摘要

我们报告了一些BCR/ABL mRNA表达变异且缺乏ABL外显子a2序列的病例。其中两例显示主要断裂点簇集区(BCR)外显子3(b3)与ABL外显子3(a3)的连接(b3/a3),而另一例显示次要BCR外显子1(e1)与a3的连接(e1/a3)。两例b3/a3连接的病例之一以及e1/a3连接的病例被诊断为急性淋巴细胞白血病,另一例b3/a3连接的病例为慢性髓性白血病。然而,其中两例被发现ABL基因的断裂点位于外显子a2和a3之间的内含子之外,可能在外显子a2的5'上游,这表明BCR外显子与ABL外显子a3进行了剪接。这些发现与先前报道的不同,先前报道中ABL基因的断裂点在外显子a2和a3之间,并且表明在形成变异型BCR/ABL融合转录本时ABL外显子a2序列缺失的一种新机制。结合先前报道的病例,讨论了在一些费城染色体阳性白血病中ABL蛋白的部分SH3区域缺失这一发现的意义。

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