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Transforming Growth Factor, Beta-1-induced 1 OKDB#: 2436
 Symbols: TGFB1I1 Species: human
 Synonyms: TRANSFORMING GROWTH FACTOR, BETA-INDUCED, 55-KD|ANDROGEN RECEPTOR COACTIVATOR, ARA55|HIC5  Locus:


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General Comment Using differential screening of a cDNA library constructed from mouse osteoblastic cells (MC3T3-E1) treated with TGFB1 (190180), Shibanuma et al. (1993) isolated several TGFB1-induced cDNAs. They stated that hydrogen peroxide was released from MC3T3-E1 cells in response to TGFB1 and was partially responsible for the TGFB1 inhibition of growth. Shibanuma et al. (1994) found that expression of one of these cDNAs was induced by hydrogen peroxide as well as by TGFB1, and therefore designated this cDNA hic5 for 'hydrogen peroxide-inducible clone 5.' The hic5 cDNA encodes a deduced 444-amino acid protein with 4 LIM motifs of the zinc finger family. Expression of hic5 was extremely reduced in several human tumor-derived cell lines and increased during cellular senescence of normal human diploid fibroblasts

General function Nucleic acid binding, DNA binding
Comment
Cellular localization Nuclear
Comment
Ovarian function
Comment
Expression regulated by FSH, LH
Comment
Ovarian localization Granulosa
Comment Rimon E, et al reported Gonadotropin-induced gene regulation in human granulosa cells obtained from IVF patients and Modulation of genes coding for growth factors and their receptors and genes involved in cancer and other diseases. Gonadotropins play a crucial role in ovarian homeostasis and fertilization. However, hypergonadotropin stimulation has been thought to increase the risk for ovarian cancer. Moreover, some correlation between high levels of gonadotropins in the circulation and Alzheimer's disease has been implicated, with no clear evidence on the molecular mechanism involved. Using DNA microarray technology and RNA from gonadotropin-stimulated human granulosa cells, which comprise the main bulk of the ovarian follicular somatic cells, we discovered that stimulation of cells with saturating doses of gonadotropins gives rise to the expression of genes coding for presenilin 1 and 2, along with the up-regulation of genes involved in steroidogenesis such as StAR, cytochrome P450scc enzyme system and aromatase. Moreover, gonadotropin stimulation in these cells dramatically elevates activity of genes coding for epiregulin and amphiregulin, which can bind and activate the EGF receptor and ERB4. These gene products may elevate the risk for ovarian, breast, endometrial and other non-gynecological cancers. Gene transcripts for oncogenes and tumor markers such as pleiomorphic adenoma gene-like 1 (Plagl1) tumor antigen (L6) and claudin 3 were markedly elevated following LH and FSH stimulation. In parallel, downregulation in ovarian cancer 1 (DOC1) and suppression of tumorigenicity (ST5) genes was observed, suggesting a potential increase for cancer development. In contrast, increase in tumor rejection antigen (gp96) 1 and decrease in connective tissue growth factor (CTGF), transforming growth factor-beta 1 induced transcript 1 (TGFB1Il), pim-1 oncogene (PIM1), v-maf musculoaponeurotic fibrosarcoma oncogene homologue (MAF) and CD24 antigen may be associated with a decreased risk for specific cancers. In conclusion, gonadotropin stimulation may modulate specific sets of gene transcripts that may either elevate or reduce the risk for specific diseases.
Follicle stages Antral, Preovulatory
Comment
Phenotypes
Mutations 0 mutations
Genomic Region show genomic region
Phenotypes and GWAS show phenotypes and GWAS
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created: April 7, 2004, 8:16 a.m. by: hsueh   email:
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last update: April 7, 2004, 8:18 a.m. by: system    email:



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