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一种与人类 LMX1(LMX1.1)相关的基因 LMX1.2 的鉴定:组织特异性表达及在 9 号染色体上的连锁定位

Identification of a human LMX1 (LMX1.1)-related gene, LMX1.2: tissue-specific expression and linkage mapping on chromosome 9.

作者信息

Iannotti C A, Inoue H, Bernal E, Aoki M, Liu L, Donis-Keller H, German M S, Permutt M A

机构信息

Department of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri 63110, USA.

出版信息

Genomics. 1997 Dec 15;46(3):520-4. doi: 10.1006/geno.1997.5075.

Abstract

LMX1 is a LIM-homeodomain (LIM-HD)-containing protein expressed selectively in insulin-producing beta-cell lines, and it it has been shown to activate insulin gene transcription. The human LMX1 gene was mapped by fluorescence in situ hybridization to chromosome region 1q22-q23, yet Church et al. (1994, Nat. Genet. 6: 98-105) identified two exon-trapping products from human chromosome 9 that were highly homologous to hamster LMX1. In the current study, we demonstrate tissue-specific expression of an LMX1 (now known as LMX1.1)-related gene, named LMX1.2. The chicken C-LMX1 gene, recently cloned using the hamster LMX1.1 sequence and shown to specify dorsal cell fate during vertebrate limb development (9), is actually more related to human LMX1.2 than LMX1.1. We have identified a unique simple sequence repeat polymorphic marker (hLMX1.2CA1) in a P1 genomic clone containing the human LMX1.2 gene and genetically mapped the marker on chromosome 9 between markers D9S1825 and D9S290 with odds of at least 1000:1. In addition, we localized the human LMX1.1 gene to three CEPH "B" yeast artificial chromosome clones (907A11, 935B12, and 947B2), along with two nearby polymorphic markers (D1S426 and D1S194)). Identification of this new LIM-HD-related gene may provide the opportunity to elucidate further the function of LIM class homeobox genes. Nearby polymorphic markers will be useful in testing the hypothesis that mutations in these LIM-HD genes result in genetic diseases such as non-insulin-dependent diabetes mellitus.

摘要

LMX1是一种含有LIM同源结构域(LIM-HD)的蛋白质,在产生胰岛素的β细胞系中选择性表达,并且已证明它能激活胰岛素基因转录。人类LMX1基因通过荧光原位杂交定位到染色体区域1q22-q23,但Church等人(1994年,《自然遗传学》6: 98-105)从人类9号染色体中鉴定出两种外显子捕获产物,它们与仓鼠LMX1高度同源。在本研究中,我们证明了一种与LMX1(现称为LMX1.1)相关的基因LMX1.2的组织特异性表达。最近利用仓鼠LMX1.1序列克隆的鸡C-LMX1基因,已证明在脊椎动物肢体发育过程中决定背侧细胞命运(9),实际上它与人类LMX1.2的关系比与LMX1.1的关系更密切。我们在一个包含人类LMX1.2基因的P1基因组克隆中鉴定出一个独特的简单序列重复多态性标记(hLMX1.2CA1),并将该标记在9号染色体上定位在标记D9S1825和D9S290之间,优势比至少为1000:1。此外,我们将人类LMX1.1基因定位到三个CEPH“B”酵母人工染色体克隆(907A11、935B12和947B2),以及两个附近的多态性标记(D1S426和D1S194)。鉴定这个新的与LIM-HD相关的基因可能为进一步阐明LIM类同源框基因的功能提供机会。附近的多态性标记将有助于检验这些LIM-HD基因中的突变导致诸如非胰岛素依赖型糖尿病等遗传疾病的假说。

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