Patched

Last updated
patched 1
Identifiers
Symbol PTCH1
Alt. symbolsNBCCS, PTCH
NCBI gene 5727
HGNC 9585
OMIM 601309
RefSeq NM_000264
UniProt Q13635
Other data
Locus Chr. 9 q22.1q31
patched 2
Identifiers
Symbol PTCH2
NCBI gene 8643
HGNC 9586
OMIM 603673
RefSeq NM_003738
UniProt Q9Y6C5
Other data
Locus Chr. 1 p34.1

Patched (Ptc) is a conserved 12-pass transmembrane protein receptor that plays an obligate negative regulatory role in the Hedgehog signaling pathway in insects and vertebrates. Patched is an essential gene in embryogenesis for proper segmentation in the fly embryo, mutations in which may be embryonic lethal. Patched functions as the receptor for the Hedgehog protein [1] and controls its spatial distribution, in part via endocytosis of bound Hedgehog protein, which is then targeted for lysosomal degradation. [2]

Contents

Discovery

The original mutations in the ptc gene were discovered in the fruit fly Drosophila melanogaster by 1995 Nobel Laureates Eric F. Wieschaus and Christiane Nusslein-Volhard and colleagues, and the gene was independently cloned in 1989 by Joan Hooper in the laboratory of Matthew P. Scott, and by Philip Ingham and colleagues.

Role in hedgehog signaling

Patched is part of a negative feedback mechanism for hedgehog signaling that helps shape the spatial gradient of signaling activity across tissues. In the absence of hedgehog, low levels of patched are sufficient to suppress activity of the signal transduction pathway. When hedgehog is present, its cholesterol moiety binds to the sterol-sensing domain in patched, which then inhibits the activity of smoothened. Smoothened is a G protein-coupled receptor, most of which is stored in membrane bound vesicles internally within the cell and which increases at the cell surface when hedgehog is present. Smoothened must be present on the cell membrane in order for the Hedgehog signaling pathway to be activated. Among other genes, the transcription of the patched gene is induced by hedgehog signaling, with the accumulation of the patched protein limiting signaling through the Smoothened protein. Recent work implicates the cilium in intracellular trafficking of hedgehog signaling components in vertebrate cells.

Role in disease

Mutated patched proteins have been implicated in a number of cancers including basal cell carcinoma, medulloblastoma, and rhabdomyosarcoma. [3] Hereditary mutations in the human patched homolog PTCH1 cause autosomal dominant Gorlin syndrome, which consists of overgrowth and hereditary disposition to cancer including basal cell carcinoma and medulloblastoma. Mice with mutations in mouse PTCH1 similarly develop medulloblastoma.

Related Research Articles

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Sonic hedgehog Protein-coding gene in the species Homo sapiens

Sonic hedgehog is a protein that in humans is encoded by the SHH gene. It is the best-studied ligand of the hedgehog signaling pathway others being desert hedgehog (DHH) and Indian hedgehog (IHH). It plays a key role in the development of animals from insects to mammals. In vertebrates it is involved in organogenesis including the growth of digits on limbs and the organization of the brain. Sonic hedgehog is an archetypal example of a morphogen as defined by Lewis Wolpert's French flag model—a molecule that diffuses to form a concentration gradient and has different effects on the cells of the developing embryo depending on its concentration. Sonic hedgehog is also active in adults; for example it controls the proliferation of adult stem cells and has been implicated in the development of some cancers.

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Cyclopamine chemical compound

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Smoothened protein-coding gene in the species Homo sapiens

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PTCH1 protein-coding gene in the species Homo sapiens

Protein patched homolog 1 is a protein that is the member of the patched family and in humans is encoded by the PTCH1 gene.

SUFU protein-coding gene in the species Homo sapiens

Suppressor of fused homolog is a protein that in humans is encoded by the SUFU gene. In molecular biology, the protein domain suppressor of fused protein (Sufu) has an important role in the cell. The Sufu is important in negatively regulating an important signalling pathway in the cell, the Hedgehog signalling pathway (HH). This particular pathway is crucial in embryonic development. There are several homologues of Sufu, found in a wide variety of organisms.

Death domain InterPro Domain

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Vismodegib chemical compound

Vismodegib is a drug for the treatment of basal-cell carcinoma (BCC). The approval of vismodegib on January 30, 2012, represents the first Hedgehog signaling pathway targeting agent to gain U.S. Food and Drug Administration (FDA) approval. The drug is also undergoing clinical trials for metastatic colorectal cancer, small-cell lung cancer, advanced stomach cancer, pancreatic cancer, medulloblastoma and chondrosarcoma as of June 2011. The drug was developed by the biotechnology/pharmaceutical company Genentech.

Philip William Ingham FRS, FMedSci, Hon. FRCP is a British geneticist, currently the Toh Kian Chui Distinguished Professor at the Lee Kong Chian School of Medicine, a partnership between Nanyang Technological University, Singapore and Imperial College, London. Previously, he was the inaugural Director of the Living Systems Institute at the University of Exeter, UK and prior to that was Vice Dean, Research at the Lee Kong Chian School of Medicine.

PTCH2 protein-coding gene in the species Homo sapiens

Patched 2 is a protein that in humans is encoded by the PTCH2 gene.

A sterol-sensing domain (SSD) is a protein domain which consists of 180 amino acids forming five transmembrane segments capable of binding sterol groups. This type of domain is present in proteins involved in cholesterol metabolism and signalling.

Hedgehog pathway inhibitors are small molecules that inhibit the activity of a component of the Hedgehog signaling pathway. Due to the role of aberrant Hedgehog signaling in tumor progression and cancer stem cell maintenance across cancer types, inhibition of the Hedgehog signaling pathway can be a useful strategy for restricting tumor growth and for preventing the recurrence of the disease post-surgery, post-radiotherapy, or post-chemotherapy. Thus, Hedgehog pathway inhibitors are an important class of anti-cancer drugs. At least three Hedgehog pathway inhibitors have been approved by the Food and Drug Administration (FDA) for cancer treatment. These include Vismodegib and Erismodegib, both inhibitors of Smoothened (SMO), which are being used for the treatment of basal cell carcinoma. Arsenic Trioxide, an inhibitor of GLI transcription factors, is being used for the treatment of acute promyelocytic leukemia. In addition, multiple other Hedgehog pathway inhibitors are in different phases of clinical trials.

References

  1. Ingham PW, Taylor AM, Nakano Y (1991). "Role of the Drosophila patched gene in positional signalling". Nature. 353 (6340): 184–7. Bibcode:1991Natur.353..184I. doi:10.1038/353184a0. PMID   1653906. S2CID   4361236.
  2. Torroja C, Gorfinkiel N, Guerrero I (2004). "Patched controls the Hedgehog gradient by endocytosis in a dynamin-dependent manner, but this internalization does not play a major role in signal transduction". Development. 131 (10): 2395–408. doi: 10.1242/dev.01102 . PMID   15102702.
  3. Pasca di Magliano M, Hebrok M (2003). "Hedgehog signalling in cancer formation and maintenance". Nat. Rev. Cancer. 3 (12): 903–11. doi:10.1038/nrc1229. PMID   14737121. S2CID   34050826.