PREB

PREB
Identifiers
AliasesPREB, SEC12, prolactin regulatory element binding
External IDsMGI: 1355326 HomoloGene: 40877 GeneCards: PREB
Gene location (Human)
Chr.Chromosome 2 (human)[1]
Band2p23.3Start27,130,756 bp[1]
End27,134,675 bp[1]
RNA expression pattern
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez

10113

50907

Ensembl

ENSG00000138073

ENSMUSG00000045302

UniProt

Q9HCU5

Q9WUQ2

RefSeq (mRNA)

NM_001330484
NM_001330485
NM_001330486
NM_001330487
NM_013388

NM_001294302
NM_016703

RefSeq (protein)

NP_001317413
NP_001317414
NP_001317415
NP_001317416
NP_037520

NP_001281231
NP_057912

Location (UCSC)Chr 2: 27.13 – 27.13 MbChr 5: 30.95 – 30.96 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Prolactin regulatory element-binding protein is a protein that in humans is encoded by the PREB gene.[5][6][7]

This gene encodes a protein that specifically binds to a Pit1-binding element of the prolactin (PRL) promoter. This protein may act as a transcriptional regulator and is thought to be involved in some of the developmental abnormalities observed in patients with partial trisomy 2p. This gene overlaps the abhydrolase domain containing 1 (ABHD1) gene on the opposite strand.[7]

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000138073 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000045302 - Ensembl, May 2017
  3. ↑ "Human PubMed Reference:".
  4. ↑ "Mouse PubMed Reference:".
  5. ↑ Fliss MS, Hinkle PM, Bancroft C (May 1999). "Expression cloning and characterization of PREB (prolactin regulatory element binding), a novel WD motif DNA-binding protein with a capacity to regulate prolactin promoter activity". Mol Endocrinol. 13 (4): 644–657. doi:10.1210/me.13.4.644. PMID 10194769.
  6. ↑ Edgar AJ (Jul 2003). "The gene structure and expression of human ABHD1: overlapping polyadenylation signal sequence with Sec12". BMC Genomics. 4: 18. doi:10.1186/1471-2164-4-18. PMC 156608. PMID 12735795.
  7. 1 2 "Entrez Gene: PREB prolactin regulatory element binding".

Further reading

  • Barrios-Rodiles M, Brown KR, Ozdamar B, et al. (2005). "High-throughput mapping of a dynamic signaling network in mammalian cells". Science. 307 (5715): 1621–1625. doi:10.1126/science.1105776. PMID 15761153.
  • Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–2127. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
  • Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–45. doi:10.1038/ng1285. PMID 14702039.
  • Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–16903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
  • Taylor Clelland CL, Levy B, McKie JM, et al. (2000). "Cloning and characterization of human PREB; a gene that maps to a genomic region associated with trisomy 2p syndrome". Mamm. Genome. 11 (8): 675–681. doi:10.1007/s003350010142. PMID 10920239.


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