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鉴定出一个基因MLL,它跨越了与人类白血病相关的11q23易位中的断点。

Identification of a gene, MLL, that spans the breakpoint in 11q23 translocations associated with human leukemias.

作者信息

Ziemin-van der Poel S, McCabe N R, Gill H J, Espinosa R, Patel Y, Harden A, Rubinelli P, Smith S D, LeBeau M M, Rowley J D

机构信息

Department of Molecular Genetics and Cell Biology, University of Chicago, IL 60637.

出版信息

Proc Natl Acad Sci U S A. 1991 Dec 1;88(23):10735-9. doi: 10.1073/pnas.88.23.10735.

Abstract

Recurring chromosomal translocations involving chromosome 11, band q23, have been observed in acute lymphoid leukemias and especially in acute myeloid leukemias. We recently showed that breakpoints in four 11q23 translocations, t(4;11)(q21;q23), t(6;11)(q27;q23), t(9;11)(p22;q23), and t(11;19)(q23;p13.3), were contained within a yeast artificial chromosome clone bearing the CD3D and CD3G gene loci. We have identified within the CD3 yeast artificial chromosome a transcription unit that spans the breakpoint junctions of the 4;11, 9;11, and 11;19 translocations, and we describe two other, related transcripts that are upregulated in the RS4;11 cell line. We have named this gene MLL (myeloid/lymphoid, or mixed-lineage, leukemia.

摘要

复发性染色体易位涉及11号染色体q23带,已在急性淋巴细胞白血病尤其是急性髓细胞白血病中观察到。我们最近发现,四个11q23易位t(4;11)(q21;q23)、t(6;11)(q27;q23)、t(9;11)(p22;q23)和t(11;19)(q23;p13.3)的断点包含在一个携带CD3D和CD3G基因座的酵母人工染色体克隆中。我们在CD3酵母人工染色体中鉴定出一个转录单元,它跨越了4;11、9;11和11;19易位的断点连接,并且我们描述了另外两个在RS4;11细胞系中上调的相关转录本。我们将这个基因命名为MLL(髓系/淋巴系或混合谱系白血病)。

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