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人过氧化物酶体增殖物激活受体γ cDNA的分离:在造血细胞中的表达及染色体定位

Isolation of the human peroxisome proliferator activated receptor gamma cDNA: expression in hematopoietic cells and chromosomal mapping.

作者信息

Greene M E, Blumberg B, McBride O W, Yi H F, Kronquist K, Kwan K, Hsieh L, Greene G, Nimer S D

机构信息

UCLA School of Medicine, Department of Medicine 90024, USA.

出版信息

Gene Expr. 1995;4(4-5):281-99.

Abstract

The nuclear receptor superfamily of transcription factors, which includes the retinoic acid receptors and v-erb A, play important roles in the molecular control of hematopoiesis. To identify nuclear receptors expressed in hematopoietic cells, we screened a human bone marrow cDNA library using a degenerate oligonucleotide and isolated a 1.85-kb full-length cDNA encoding a new human member of this superfamily, the peroxisome proliferator activated receptor gamma (hPPAR gamma). Two different hPPAR gamma transcripts were expressed in hematopoietic cells: a 1.85-kb transcript, which corresponds to the full-length mRNA (PPAR gamma 1), and a 0.65-kb transcript (PPAR gamma 2), which cannot encode all of the nuclear receptor functional domains. Normal neutrophils and peripheral blood lymphocytes, as well as circulating leukemic cells from patients with AML, ALL, and CML, express only PPAR gamma 2 on Northern blot analysis. In contrast, only the PPAR gamma 1 transcript was detected in a variety of human leukemia cell lines and in cultured normal primary bone marrow stromal cells. Both transcripts were detected in various fetal and adult nonhematopoietic tissues. We mapped the location of the hPPAR gamma gene to human chromosome 3p25 by somatic cell hybridization and linkage analysis. PPARs have been shown to be activated by peroxisome proliferating agents, long-chain fatty acids and arachidonic acid. Human PPAR gamma, although homologous to the PPAR gamma s of other species, has unique sequence and amino acid differences. Identification of hPPAR gamma will allow further understanding of its role in human cellular leukotriene, prostaglandin, and peroxide degradative or synthetic pathways, as well as its role in lipid metabolism and regulation of adipocyte differentiation.

摘要

转录因子的核受体超家族,包括维甲酸受体和v-erb A,在造血的分子调控中发挥重要作用。为了鉴定造血细胞中表达的核受体,我们使用简并寡核苷酸筛选了人骨髓cDNA文库,并分离出一个1.85 kb的全长cDNA,其编码该超家族的一个新的人类成员,即过氧化物酶体增殖物激活受体γ(hPPARγ)。造血细胞中表达两种不同的hPPARγ转录本:一种1.85 kb的转录本,对应全长mRNA(PPARγ1),另一种0.65 kb的转录本(PPARγ2),其不能编码所有的核受体功能结构域。Northern印迹分析显示,正常中性粒细胞和外周血淋巴细胞,以及急性髓细胞白血病、急性淋巴细胞白血病和慢性髓细胞白血病患者的循环白血病细胞仅表达PPARγ2。相反,在多种人类白血病细胞系和培养的正常原代骨髓基质细胞中仅检测到PPARγ1转录本。在各种胎儿和成人非造血组织中均检测到这两种转录本。我们通过体细胞杂交和连锁分析将hPPARγ基因定位到人类染色体3p25。过氧化物酶体增殖物激活受体已被证明可被过氧化物酶体增殖剂、长链脂肪酸和花生四烯酸激活。人PPARγ虽然与其他物种的PPARγ同源,但具有独特的序列和氨基酸差异。hPPARγ的鉴定将有助于进一步了解其在人类细胞白三烯、前列腺素和过氧化物降解或合成途径中的作用,以及其在脂质代谢和脂肪细胞分化调控中的作用。

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Peroxisome proliferator-activated receptors and lipid metabolism.过氧化物酶体增殖物激活受体与脂质代谢
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