1. Gene
  2. ZBTB33 - zinc finger and BTB domain containing 33 Gene

ZBTB33 - zinc finger and BTB domain containing 33 Gene

中文名称:含锌指和 BTB 域 33

种属: Homo sapiens

同用名: ZNF348; ZNF-kaiso

基因 ID: 10009 | 基因类型: protein coding

关于 ZBTB33

Cytogenetic location: Xq24 Genomic coordinates (GRCh38): X:120,250,812-120,258,398 (from NCBI)

This gene has 2 transcripts (splice variants), 206 orthologues and 28 paralogues. Ubiquitous expression in skin (RPKM 10.2), bone marrow (RPKM 8.2) and 25 other tissues.

功能概要

该基因编码具有双峰 DNA 结合特异性的转录调节因子,它结合甲基化的 CGCG 和非甲基化的共有 KAISO 结合位点 TCCTGCNA。该蛋白质包含一个 N 端 POZ/BTB 结构域和 3 个 C 端锌指基序。它募集 N-CoR 阻遏物复合物以促进组蛋白去乙酰化和靶基因启动子中抑制染色质结构的形成。它可能有助于抑制 Wnt 信号通路的靶基因,也可能通过募集连环蛋白 delta-2 (CTNND2) 激活靶基因子集的转录。它与连环蛋白 delta-1 (CTNND1) 的相互作用抑制与甲基化和非甲基化 DNA 的结合。它还直接与核输入受体 Importin-#945;2 (也称为 karyopherin alpha2 或 RAG 队列 1) 相互作用,这可能介导该蛋白质的核输入。已经鉴定出编码相同蛋白质的可变剪接转录本变体。[RefSeq 提供,2010 年 5 月]

This gene encodes a transcriptional regulator with bimodal DNA-binding specificity, which binds to methylated CGCG and also to the non-methylated consensus KAISO-binding site TCCTGCNA. The protein contains an N-terminal POZ/BTB domain and 3 C-terminal zinc finger motifs. It recruits the N-CoR repressor complex to promote histone deacetylation and the formation of repressive chromatin structures in target gene promoters. It may contribute to the repression of target genes of the Wnt signaling pathway, and may also activate transcription of a subset of target genes by the recruitment of catenin delta-2 (CTNND2). Its interaction with catenin delta-1 (CTNND1) inhibits binding to both methylated and non-methylated DNA. It also interacts directly with the nuclear import receptor Importin-α2 (also known as karyopherin alpha2 or RAG cohort 1), which may mediate nuclear import of this protein. Alternatively spliced transcript variants encoding the same protein have been identified.[provided by RefSeq, May 2010]

ZBTB33 基因产物(2)

mRNA Protein Name
NM_001184742.2 NP_001171671.1 transcriptional regulator Kaiso
NM_006777.4 NP_006768.1 transcriptional regulator Kaiso
基因本体论
  • 分子功能
  • 生物过程
分子功能 GO 注释 逻辑证据 参考文献 来源
enables methyl-CpG binding IDA
IDA: 通过直接分析推断
16354688 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
10207085 GOA
enables sequence-specific DNA binding IDA
IDA: 通过直接分析推断
20403812 GOA
enables sequence-specific double-stranded DNA binding IDA
IDA: 通过直接分析推断
28473536 GOA
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in negative regulation of DNA-templated transcription IDA
IDA: 通过直接分析推断
16354688 GOA
involved in negative regulation of DNA-templated transcription IMP
IMP: 通过突变表型推断
23251453 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

ZBTB33 蛋白结构

BTB

BTB: BTB/POZ domain (22 - 114)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (508 - 531)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (538 - 560)

  • 0
  • 200
  • 400
  • 600
  • 672 a.a.
蛋白主名 其他名称

transcriptional regulator Kaiso

WUGSC:H_DJ525N14.1

ZBTB33 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
种属内
ZBTB33 Q86T24 NUDT22 Homo sapiens Q9BRQ3
Validated Y2H
32296183
种属内
ZBTB33 Q86T24 TRIML2 Homo sapiens Q8N7C3
Anti Tag CoIP
26496610
种属内
ZBTB33 Q86T24 TRIML2 Homo sapiens Q8N7C3
Validated Y2H
32296183
种属间: 跨种属相互作用 种属内: 同种属相互作用

ZBTB33 抗体

目录号 产品名 应用 反应物种
HY-P82798 Kaiso Antibody (YA2543) WB Human, Mouse, Rat

关联疾病

疾病名称 别名
Rett Syndrome

Atypical Rett Syndrome

RTT

Rett Disorder

Rts

Autism, Dementia, Ataxia, And Loss Of Purposeful Hand Use

Rett Syndrome, Preserved Speech Variant

Rett Syndrome, Atypical

Rett'S Disorder

Rett Syndrome Variant

Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use Syndrome

Cerebroatrophic Hyperammonemia

Rett Like Syndrome

Rett'S Syndrome

Atypical Rtt

Autism-Dementia-Ataxia-Loss Of Purposeful Hand Use

Rett Syndrome Preserved Speech Variant

Rett Syndrome Zappella Variant

Rett Syndrome, Zappella Variant

Cri-Du-Chat Syndrome

5p Deletion Syndrome

5p Partial Monosomy Syndrome

Monosomy 5p

Cat Cry Syndrome

Chromosome 5p Deletion Syndrome

Cri Du Chat Syndrome

5p- Syndrome

5p Minus Syndrome

Chromosome 5p- Syndrome

Chromosome 5 Short Arm Deletion Syndrome

Chromosome 5p Deletion

Deletion 5p

Cri Du Chat

5p Partial Deletion Syndrome

Partial Deletion Of Short Arm Of Chromosome 5 Syndrome

疾病名称 别名
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

直系同源

种属 基因名 来源 基因 ID
Mus musculus ZBTB33 MGD MGI:1927290
Canis familiaris ZBTB33 VGNC VGNC:48531
Rattus norvegicus ZBTB33 RGD RGD:1566309
Felis catus ZBTB33 VGNC VGNC:67165
Macaca mulatta ZBTB33 VGNC VGNC:79043
Bos taurus ZBTB33 VGNC VGNC:37073