| general transcription factor IIH, polypeptide 1, 62kDa | |
| Hgncid: | 4655 |
| Symbol: | GTF2H1 |
| Altsymbols: | BTF2 |
| Entrezgene: | 2965 |
| Omim: | 189972 |
| Refseq: | NM_005316 |
| Uniprot: | P32780 |
| Chromosome: | 11 |
| Arm: | p |
| Band: | 15.1 |
| Locussupplementarydata: | -p14 |
| general transcription factor IIH, polypeptide 2, 44kDa | |
| Hgncid: | 4656 |
| Symbol: | GTF2H2 |
| Altsymbols: | BTF2, TFIIH, BTF2P44, T-BTF2P44 |
| Entrezgene: | 2966 |
| Omim: | 601748 |
| Refseq: | NM_001515 |
| Uniprot: | Q13888 |
| Chromosome: | 5 |
| Arm: | q |
| Band: | 12.2 |
| Locussupplementarydata: | -13.3 |
| general transcription factor IIH, polypeptide 3, 34kDa | |
| Hgncid: | 4657 |
| Symbol: | GTF2H3 |
| Altsymbols: | BTF2, TFIIH |
| Entrezgene: | 2967 |
| Omim: | 601750 |
| Refseq: | NM_001516 |
| Uniprot: | Q13889 |
| Chromosome: | 12 |
| Arm: | q |
| Band: | 24.31 |
Transcription factor II H (TFIIH) is an important protein complex, having roles in transcription of various protein-coding genes and DNA nucleotide excision repair (NER) pathways. TFIIH first came to light in 1989 when general transcription factor-δ or basic transcription factor 2 was characterized as an indispensable transcription factor in vitro. This factor was also isolated from yeast and finally named TFIIH in 1992.[1] [2]
TFIIH consists of ten subunits, 7 of which (ERCC2/XPD, ERCC3/XPB, GTF2H1/p62, GTF2H4/p52, GTF2H2/p44, GTF2H3/p34 and GTF2H5/TTDA) form the core complex. The cyclin-activating kinase-subcomplex (CDK7, MAT1, and cyclin H) is linked to the core via the XPD protein.[3] Two of the subunits, ERCC2/XPD and ERCC3/XPB, have helicase and ATPase activities and help create the transcription bubble. In a test tube, these subunits are only required for transcription if the DNA template is not already denatured or if it is supercoiled.
Two other TFIIH subunits, CDK7 and cyclin H, phosphorylate serine amino acids on the RNA polymerase II C-terminal domain and possibly other proteins involved in the cell cycle. Next to a vital function in transcription initiation, TFIIH is also involved in nucleotide excision repair.
Before TFIIH identified it, it had several names. It was isolated in 1989 isolated from rat liver, known by factor transcription delta. When identified from cancer cells it was known that time as Basic transcription factor 2. Also, when isolated from yeast it was termed transcription factor B. Finally, in 1992 known as TFIIH.[4]
TFIIH is a ten‐subunit complex; seven of these subunits comprise the “core” whereas three comprise the dissociable “CAK” (CDK Activating Kinase) module.[5] The core consists of subunits XPB, XPD, p62, p52, p44, p34 and p8 while CAK is composed of CDK7, cyclin H, and MAT1.[6]
General function of TFIIH:
(NER)TFIIH is a general transcription factor that acts to recruit RNA Pol II to the promoters of genes. It functions as a helicase that unwinds DNA. It also unwinds DNA after a DNA lesion has been recognized by either the global genome repair (GGR) pathway or the transcription-coupled repair (TCR) pathway of NER.[8] [9] Purified TFIIH has role in stopping further RNA synthesis by activating the cyclic peptide α-amanitin.
Mutation in genes (XPB), (XPD) or (TTDA) cause trichothiodystrophy, a condition characterized by photosensitivity, ichthyosis, brittle hair and nails, intellectual impairment, decreased fertility and/or short stature.[10]
Genetic polymorphisms of genes that encode subunits of TFIIH are known to be associated with increased cancer susceptibility in many tissues, e.g.; skin tissue, breast tissue and lung tissue. Mutations in the subunits (such as XPD and XPB) can lead to a variety of diseases, including xeroderma pigmentosum (XP) or XP combined with Cockayne syndrome.[11] In addition to genetic variations, virus-encoded proteins also target TFIIH.[12]
TFIIH participates in nucleotide excision repair (NER) by opening the DNA double helix after damage is initially recognized. NER is a multi-step pathway that removes a wide range of different damages that distort normal base pairing, including bulky chemical damages and UV-induced damages. Individuals with mutational defects in genes specifying protein components that catalyze the NER pathway, including the TFIIH components, often display features of premature aging[13] (see DNA damage theory of aging).
Potent, bioactive natural products like triptolide that inhibit mammalian transcription via inhibition of the XPB subunit of the general transcription factor TFIIH has been recently reported as a glucose conjugate for targeting hypoxic cancer cells with increased glucose transporter expression.[14]