• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Cloning and sequencing of the mouse Gli2 gene: localization to the Dominant hemimelia critical region.

作者信息

Hughes D C, Allen J, Morley G, Sutherland K, Ahmed W, Prosser J, Lettice L, Allan G, Mattei M G, Farrall M, Hill R E

机构信息

MRC Human Genetics Unit, Western General Hospital, Edinburgh, United Kingdom.

出版信息

Genomics. 1997 Jan 15;39(2):205-15. doi: 10.1006/geno.1996.4468.

DOI:10.1006/geno.1996.4468
PMID:9027508
Abstract

The GLI family of zinc finger genes has been implicated in both neoplastic and developmental disorders. We have cloned and sequenced the mouse homolog of the zinc finger gene Gli2 and demonstrated significant similarity to the human GLI3 gene. We have also localized Gli2 to mouse chromosome 1, in the vicinity of the morphogenetic mutation Dominant hemimelia (Dh), which is characterized by tibial hemimelia, poly/oligodactyly, and a number of visceral abnormalities, most strikingly absence of the spleen. Using a Gli2-associated microsatellite, we demonstrated no recombination between Dh and Gli2 in a Dh intraspecific backcross. Gli2 is expressed in Dh heterozygotes and homozygotes. However, using a combination of mismatch analysis and direct sequencing, we have failed to identify any mutations in the coding sequence of Gli2 from Dh. We have also demonstrated that it is unlikely that there are any Gli genes in the mouse genome in addition to the previously described Gli, Gli2, and Gli3.

摘要

相似文献

1
Cloning and sequencing of the mouse Gli2 gene: localization to the Dominant hemimelia critical region.
Genomics. 1997 Jan 15;39(2):205-15. doi: 10.1006/geno.1996.4468.
2
Cloning and characterization of ZNF189, a novel human Krüppel-like zinc finger gene localized to chromosome 9q22-q31.ZNF189的克隆与鉴定,ZNF189是一个定位于9号染色体q22 - q31区域的新型人类类Krüppel锌指基因。
Genomics. 1998 Jun 1;50(2):213-21. doi: 10.1006/geno.1998.5309.
3
GLI3 frameshift mutations cause autosomal dominant Pallister-Hall syndrome.GLI3 移码突变导致常染色体显性遗传的帕利斯特-霍尔综合征。
Nat Genet. 1997 Mar;15(3):266-8. doi: 10.1038/ng0397-266.
4
Gli3 expression is affected in the morphogenetic mouse mutants add and Xt.Gli3基因的表达在形态发生小鼠突变体add和Xt中受到影响。
Prog Clin Biol Res. 1993;383A:153-61.
5
GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families.GLI3锌指基因在Greig综合征家族中因易位而中断。
Nature. 1991 Aug 8;352(6335):539-40. doi: 10.1038/352539a0.
6
Isolation of a yeast artificial chromosome contig spanning the Greig cephalopolysyndactyly syndrome (GCPS) gene region.跨越Greig头多指(趾)综合征(GCPS)基因区域的酵母人工染色体重叠群的分离。
Genomics. 1994 Aug;22(3):563-8. doi: 10.1006/geno.1994.1429.
7
Interplays of Gli2 and Gli3 and their requirement in mediating Shh-dependent sclerotome induction.Gli2和Gli3的相互作用及其在介导Shh依赖性体节诱导中的作用。
Development. 2003 Dec;130(25):6233-43. doi: 10.1242/dev.00851. Epub 2003 Nov 5.
8
Analysis of homologous XRCC1-linked zinc-finger gene families in human and mouse: evidence for orthologous genes.人类和小鼠中同源XRCC1连接锌指基因家族的分析:直系同源基因的证据。
Genomics. 1998 Apr 1;49(1):112-21. doi: 10.1006/geno.1998.5230.
9
Regulation of Gli2 and Gli3 activities by an amino-terminal repression domain: implication of Gli2 and Gli3 as primary mediators of Shh signaling.氨基末端抑制结构域对Gli2和Gli3活性的调控:Gli2和Gli3作为Shh信号主要介导因子的意义
Development. 1999 Sep;126(17):3915-24. doi: 10.1242/dev.126.17.3915.
10
Cloning and characterization of ZNF236, a glucose-regulated Kruppel-like zinc-finger gene mapping to human chromosome 18q22-q23.ZNF236的克隆与特性分析,ZNF236是一个定位于人类染色体18q22 - q23的葡萄糖调节型类克鲁ppel锌指基因。
Genomics. 1999 Aug 15;60(1):105-9. doi: 10.1006/geno.1999.5897.

引用本文的文献

1
The Role of Smoothened-Dependent and -Independent Hedgehog Signaling Pathway in Tumorigenesis.平滑依赖型和非依赖型刺猬信号通路在肿瘤发生中的作用
Biomedicines. 2021 Sep 10;9(9):1188. doi: 10.3390/biomedicines9091188.
2
Molecular characterization and genome-wide mutations in porcine anal atresia candidate gene GLI2.猪肛门闭锁候选基因 GLI2 的分子特征和全基因组突变。
Mamm Genome. 2013 Dec;24(11-12):500-7. doi: 10.1007/s00335-013-9485-8. Epub 2013 Nov 10.
3
Sonic Hedgehog signaling is a positive oligodendrocyte regulator during demyelination.
Sonic Hedgehog 信号在脱髓鞘过程中是一种正向的少突胶质细胞调节因子。
J Neurosci. 2013 Jan 30;33(5):1759-72. doi: 10.1523/JNEUROSCI.3334-12.2013.
4
A new locus for split hand/foot malformation with long bone deficiency (SHFLD) at 2q14.2 identified from a chromosome translocation.从染色体易位中鉴定出位于2q14.2的手足裂畸形伴长骨缺损(SHFLD)的新基因座。
Hum Genet. 2007 Sep;122(2):191-9. doi: 10.1007/s00439-007-0390-7. Epub 2007 Jun 14.
5
A potential role of alternative splicing in the regulation of the transcriptional activity of human GLI2 in gonadal tissues.可变剪接在性腺组织中对人GLI2转录活性调控中的潜在作用。
BMC Mol Biol. 2006 Mar 23;7:13. doi: 10.1186/1471-2199-7-13.
6
GLIS3, a novel member of the GLIS subfamily of Krüppel-like zinc finger proteins with repressor and activation functions.GLIS3,一种具有抑制和激活功能的Krüppel样锌指蛋白GLIS亚家族的新成员。
Nucleic Acids Res. 2003 Oct 1;31(19):5513-25. doi: 10.1093/nar/gkg776.
7
Hedgehog signaling in mouse mammary gland development and neoplasia.
J Mammary Gland Biol Neoplasia. 2001 Jan;6(1):53-66. doi: 10.1023/a:1009516515338.
8
Vertebrate homologs of Drosophila suppressor of fused interact with the gli family of transcriptional regulators.果蝇融合抑制因子的脊椎动物同源物与转录调节因子Gli家族相互作用。
Dev Biol. 1999 Aug 15;212(2):323-36. doi: 10.1006/dbio.1999.9335.
9
Cloning of novel isoforms of the human Gli2 oncogene and their activities to enhance tax-dependent transcription of the human T-cell leukemia virus type 1 genome.人类Gli2癌基因新亚型的克隆及其增强人类1型T细胞白血病病毒基因组tax依赖性转录的活性。
J Virol. 1998 May;72(5):3958-64. doi: 10.1128/JVI.72.5.3958-3964.1998.