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多种同源框基因在不同哺乳动物造血谱系中的表达。

Expression of multiple homeobox genes within diverse mammalian haemopoietic lineages.

作者信息

Kongsuwan K, Webb E, Housiaux P, Adams J M

机构信息

Walter and Eliza Hall Institute of Medical Research, Post Office Royal Melbourne Hospital, Victoria, Australia.

出版信息

EMBO J. 1988 Jul;7(7):2131-8. doi: 10.1002/j.1460-2075.1988.tb03052.x.

DOI:10.1002/j.1460-2075.1988.tb03052.x
PMID:2901346
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC454515/
Abstract

Several mouse and human genes encoding the DNA-binding homeobox domain are implicated here in haematopoiesis, a differentiation process maintained throughout life. Four homeobox cDNA clones were isolated from bone marrow and spleen of adult mice and two from the human leukaemia cell line K562. They derive from the Hox 1.1, Hox 2.3, Hox 6.1 genes and two previously undescribed genes, one of a type (paired) not found before in vertebrates. A survey of 36 cell lines of the lymphoid, myeloid and erythroid lineages revealed that certain homeobox transcripts were almost ubiquitous, while others were restricted to certain lineages or even particular cell lines. The expression pattern altered in a myeloid and an erythroid line induced to terminal differentiation, and in novel lines that had switched from a lymphoid to a myeloid phenotype. Altogether, the haemopoietic compartment may contain up to 20 homeobox transcripts. In one myeloid leukaemia, DNA rearrangement has perturbed expression. These findings suggest that homeobox genes may influence developmental decisions within the haemopoietic system.

摘要

几个编码DNA结合同源异型框结构域的小鼠和人类基因与造血作用有关,造血作用是一种贯穿生命始终的分化过程。从成年小鼠的骨髓和脾脏中分离出四个同源异型框cDNA克隆,从人类白血病细胞系K562中分离出两个。它们源自Hox 1.1、Hox 2.3、Hox 6.1基因以及两个之前未描述的基因,其中一个是脊椎动物中以前未发现的类型(配对型)。对36个淋巴系、髓系和红系细胞系的调查显示,某些同源异型框转录本几乎普遍存在,而其他转录本则局限于某些细胞系甚至特定细胞系。在诱导至终末分化的髓系和红系细胞系中,以及在从淋巴样表型转变为髓样表型的新细胞系中,表达模式发生了改变。总的来说,造血区室可能包含多达20种同源异型框转录本。在一种髓系白血病中,DNA重排扰乱了表达。这些发现表明同源异型框基因可能影响造血系统内的发育决定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffd8/454515/12fac93b0b75/emboj00144-0208-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffd8/454515/35c79adfa73e/emboj00144-0206-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffd8/454515/bc962511488e/emboj00144-0206-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffd8/454515/2a3d8df56861/emboj00144-0208-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffd8/454515/12fac93b0b75/emboj00144-0208-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffd8/454515/35c79adfa73e/emboj00144-0206-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffd8/454515/bc962511488e/emboj00144-0206-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffd8/454515/2a3d8df56861/emboj00144-0208-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffd8/454515/12fac93b0b75/emboj00144-0208-b.jpg

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