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pcr芯片
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上海英拜
Hippo信号通路PCR芯片可用于研究与Hippo信号通路相关的84个基因的表达情况。
The Human Hippo Signaling Pathway RT² Profiler PCR Array profiles the expression of 84 genes involved in the Hippo signal transduction cascade. The evolutionarily conserved Hippo pathway was discovered by analyzing Drosophila mutations with overgrown tissues, and mammalian homologues of its components have since been identified and characterized at a molecular level. The Hippo cascade regulates organ size and stem cell properties by governing cell proliferation, apoptosis, and contact inhibition. Alterations of this pathway are frequently found associated with cell overgrowth and tumorigenesis. The Hippo pathway can be divided into upstream regulatory components, the Hippo core kinase components, and the downstream transcriptional machinery for modulating target gene expression. Multiple proteins, some of which mediate cell-cell or cell-ECM adhesion, feed into the core of the Hippo pathway. Upstream regulators such as WWC1, SCRIB, Crumbs complex, cadherins, FAT, and Dachsous modulate the Hippo pathway by activating the core kinase cassette. There, autophosphorylated MST1/2 catalyzes the phosphorylation and activation of LATS1/2 that in turn catalyzes the phosphorylation of the transcriptional co-activators YAP1 and TAZ. In their unphosphorylated states, YAP1 and TAZ freely enter the nucleus and function as transcriptional co-activators. However upon phosphorylation, YAP1 and TAZ instead bind the 14-3-3 family of scaffolding proteins, sequestering them in the cytosol. Upstream regulators can also circumvent the core kinase cassette by sequestering the co-activators at cell-cell junctions instead. This array profiles genes involved in upstream regulation, the core kinase complex, and downstream mediation of the Hippo pathway. A set of controls present on each array enables data analysis using the ΔΔCT method of relative quantification and assessment of reverse transcription performance, genomic DNA contamination, and PCR performance. Using real-time PCR, research studies can easily and reliably analyze components of the Hippo signaling pathway with this array.
Upstream Regulators: ACTG1, AMOT, AMOTL1, AMOTL2, CASP3, CRB1, CRB2, CRB3, CSNK1D, CSNK1E, DCHS1, DCHS2, DIAPH2, DLG1, DVL2, FAT1, FAT2, FAT3, FAT4, FJX1, JUB, LIMD1, LIX1L, LLGL1, LLGL2, LPP, NF2, RASSF4, SCRIB, WTIP, WWC1, ZDHHC18.
Hippo Core Kinase Complex: LATS2, MOBKL1A, MOBKL1B, SAV1, STK3, STK4, TAZ, YAP1, MST1, WWTR1.
Downstream Mediators: HIPK2, MAPK10, MEIS1, PRKCI, PRKCZ, SMAD1, TEAD1, TEAD2, TEAD3, TEAD4, TP63, TSHZ1, TSHZ2, TSHZ3, WNT1.
Target Genes: CASP3, CCNE1, CCNE2, MYC, PPP2CB, PPP2R1A, PPP2R2D, PTPN14, RERE.
Contact Inhibition: NF2, TAZ, YAP1.
Cell Polarity: CRB1, CRB2, CRB3, DCHS1, DCHS2, FAT1, FAT2, FAT3, FAT4, LATS1, LATS2, MST1, SCRIB, STK3, STK4, GPC5, HMCN1, POTEE, POTEI, TAOK1, TAOK2, TAOK3, TJP1, TJP2, MPDZ, MPP5, NPHP4, PARD3, PARD6G.
Scaffolding Proteins: YWHAB, YWHAE, YWHAQ, YWHAZ.
The Human Hippo Signaling Pathway RT² Profiler PCR Array profiles the expression of 84 genes involved in the Hippo signal transduction cascade. The evolutionarily conserved Hippo pathway was discovered by analyzing Drosophila mutations with overgrown tissues, and mammalian homologues of its components have since been identified and characterized at a molecular level. The Hippo cascade regulates organ size and stem cell properties by governing cell proliferation, apoptosis, and contact inhibition. Alterations of this pathway are frequently found associated with cell overgrowth and tumorigenesis. The Hippo pathway can be divided into upstream regulatory components, the Hippo core kinase components, and the downstream transcriptional machinery for modulating target gene expression. Multiple proteins, some of which mediate cell-cell or cell-ECM adhesion, feed into the core of the Hippo pathway. Upstream regulators such as WWC1, SCRIB, Crumbs complex, cadherins, FAT, and Dachsous modulate the Hippo pathway by activating the core kinase cassette. There, autophosphorylated MST1/2 catalyzes the phosphorylation and activation of LATS1/2 that in turn catalyzes the phosphorylation of the transcriptional co-activators YAP1 and TAZ. In their unphosphorylated states, YAP1 and TAZ freely enter the nucleus and function as transcriptional co-activators. However upon phosphorylation, YAP1 and TAZ instead bind the 14-3-3 family of scaffolding proteins, sequestering them in the cytosol. Upstream regulators can also circumvent the core kinase cassette by sequestering the co-activators at cell-cell junctions instead. This array profiles genes involved in upstream regulation, the core kinase complex, and downstream mediation of the Hippo pathway. A set of controls present on each array enables data analysis using the ΔΔCT method of relative quantification and assessment of reverse transcription performance, genomic DNA contamination, and PCR performance. Using real-time PCR, research studies can easily and reliably analyze components of the Hippo signaling pathway with this array.
| Product | Species | Technology | Cat. No. |
| Drug Metabolism PCR Array | Human | Gene Expression | PAHS-002Z |
| Drug Metabolism PCR Array | Mouse | Gene Expression | PAMM-002Z |
| Drug Metabolism PCR Array | Rat | Gene Expression | PARN-002Z |
Upstream Regulators: ACTG1, AMOT, AMOTL1, AMOTL2, CASP3, CRB1, CRB2, CRB3, CSNK1D, CSNK1E, DCHS1, DCHS2, DIAPH2, DLG1, DVL2, FAT1, FAT2, FAT3, FAT4, FJX1, JUB, LIMD1, LIX1L, LLGL1, LLGL2, LPP, NF2, RASSF4, SCRIB, WTIP, WWC1, ZDHHC18.
Hippo Core Kinase Complex: LATS2, MOBKL1A, MOBKL1B, SAV1, STK3, STK4, TAZ, YAP1, MST1, WWTR1.
Downstream Mediators: HIPK2, MAPK10, MEIS1, PRKCI, PRKCZ, SMAD1, TEAD1, TEAD2, TEAD3, TEAD4, TP63, TSHZ1, TSHZ2, TSHZ3, WNT1.
Target Genes: CASP3, CCNE1, CCNE2, MYC, PPP2CB, PPP2R1A, PPP2R2D, PTPN14, RERE.
Contact Inhibition: NF2, TAZ, YAP1.
Cell Polarity: CRB1, CRB2, CRB3, DCHS1, DCHS2, FAT1, FAT2, FAT3, FAT4, LATS1, LATS2, MST1, SCRIB, STK3, STK4, GPC5, HMCN1, POTEE, POTEI, TAOK1, TAOK2, TAOK3, TJP1, TJP2, MPDZ, MPP5, NPHP4, PARD3, PARD6G.
Scaffolding Proteins: YWHAB, YWHAE, YWHAQ, YWHAZ.
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了 Hippo 与 ERα 的关系。YAP1/TEAD4 可以作为 ERα 的辅因子,促进 ERα 相关增强子的激活,从而促进 ERα 下游信号通路的激活及 ER + 乳腺癌的进展 [5]。ERα 亦对 Hippo 通路有影响:ER + 乳腺癌中,CRABP2 可以结合 LATS1 并抑制其泛素化降解,从而抑制 YAP/TAZ 的核转位;但 ER - 乳腺癌中,CRABP2 反而促进 LATS1 泛素化降解,促进 YAP/TAZ 的活化,但具体机制尚不明确 [6]。这些研究成果说明,ER + 乳
Hippo信号通路PCR芯片Hippo Signaling PCR Array
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