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从人类表皮分化复合体中对新型皮肤特异性基因进行定位克隆。

Positional cloning of novel skin-specific genes from the human epidermal differentiation complex.

作者信息

Zhao X P, Elder J T

机构信息

Department of Dermatology, University of Michigan, Ann Arbor, Michigan 48109, USA.

出版信息

Genomics. 1997 Oct 15;45(2):250-8. doi: 10.1006/geno.1997.4952.

Abstract

The epidermal differentiation complex, located on human chromosomal band 1q21, contains at least 20 genes expressed during epidermal differentiation. We constructed a 1.2-Mb YAC contig spanning the SPRR and S100 gene clusters. Restriction mapping and FISH confirmed the colinearity of the contig with the genomic restriction map (A. Volz et al., 1993, Genomics 18:92-99). However, the YAC clones revealed several additional restriction sites not previously detected in genomic DNA, presumably due to CpG methylation. Making use of cDNA selection, we have identified three novel cDNAs, all of which map to the SPRR/IVL region. All three transcripts are expressed at high levels in normal and psoriatic skin, but not in cultured keratinocytes or in a variety of cell lines and human tissues. The molecular cloning of this region provides a valuable tool for identifying additional epidermal differentiation genes and for elucidating the relationship between chromatin structure and gene expression during terminal differentiation.

摘要

位于人类染色体1q21带上的表皮分化复合体包含至少20个在表皮分化过程中表达的基因。我们构建了一个跨越SPRR和S100基因簇的1.2兆碱基对的酵母人工染色体(YAC)重叠群。限制性酶切图谱分析和荧光原位杂交(FISH)证实了该重叠群与基因组限制性图谱的共线性(A. 沃尔兹等人,1993年,《基因组学》18:92 - 99)。然而,YAC克隆显示出几个先前在基因组DNA中未检测到的额外限制性酶切位点,推测这是由于CpG甲基化所致。利用cDNA筛选技术,我们鉴定出了三个新的cDNA,它们均定位于SPRR/IVL区域。这三个转录本在正常皮肤和银屑病皮肤中均高水平表达,但在培养的角质形成细胞、多种细胞系及人体组织中不表达。该区域的分子克隆为鉴定其他表皮分化基因以及阐明终末分化过程中染色质结构与基因表达之间的关系提供了一个有价值的工具。

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