CAMP responsive element modulator

Protein-coding gene in the species Homo sapiens
CREM
Identifiers
AliasesCREM, CREM-2, ICER, hCREM-2, cAMP responsive element modulator
External IDsOMIM: 123812 MGI: 88495 HomoloGene: 84591 GeneCards: CREM
Gene location (Human)
Chromosome 10 (human)
Chr.Chromosome 10 (human)[1]
Chromosome 10 (human)
Genomic location for CREM
Genomic location for CREM
Band10p11.21Start35,126,791 bp[1]
End35,212,958 bp[1]
Gene location (Mouse)
Chromosome 18 (mouse)
Chr.Chromosome 18 (mouse)[2]
Chromosome 18 (mouse)
Genomic location for CREM
Genomic location for CREM
Band18|18 A1Start3,266,048 bp[2]
End3,337,748 bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • sperm

  • gallbladder

  • anterior pituitary

  • left uterine tube

  • islet of Langerhans

  • right lung

  • left ventricle

  • stromal cell of endometrium

  • caudate nucleus

  • canal of the cervix
Top expressed in
  • spermatid

  • spermatocyte

  • seminiferous tubule

  • adrenal gland

  • proximal tubule

  • islet of Langerhans

  • atrioventricular valve

  • endocardial cushion

  • left lobe of liver

  • temporal muscle
More reference expression data
BioGPS




More reference expression data
Gene ontology
Molecular function
  • DNA binding
  • cAMP response element binding protein binding
  • DNA-binding transcription factor activity
  • protein binding
  • RNA polymerase II transcription regulatory region sequence-specific DNA binding
  • DNA-binding transcription repressor activity, RNA polymerase II-specific
  • DNA-binding transcription factor activity, RNA polymerase II-specific
Cellular component
  • cytoplasm
  • transcription regulator complex
  • nucleus
Biological process
  • cell differentiation
  • regulation of transcription, DNA-templated
  • glycosphingolipid metabolic process
  • rhythmic process
  • transcription, DNA-templated
  • fatty acid metabolic process
  • multicellular organism development
  • retinoic acid receptor signaling pathway
  • regulation of circadian rhythm
  • spermatogenesis
  • glucose metabolic process
  • positive regulation of transcription by RNA polymerase II
  • signal transduction
  • negative regulation of transcription by RNA polymerase II
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

1390

12916

Ensembl

ENSG00000095794

ENSMUSG00000063889

UniProt

Q03060

P27699

RefSeq (mRNA)
NM_001267562
NM_001267563
NM_001267564
NM_001267565
NM_001267566

NM_001267567
NM_001267568
NM_001267569
NM_001267570
NM_001881
NM_181571
NM_182717
NM_182718
NM_182719
NM_182720
NM_182721
NM_182722
NM_182723
NM_182724
NM_182725
NM_182769
NM_182770
NM_182771
NM_182772
NM_182850
NM_182853
NM_183011
NM_183012
NM_183013
NM_183060
NM_001352445
NM_001352446
NM_001352465
NM_001352466
NM_001352467
NM_001394595
NM_001394598
NM_001394600
NM_001394602
NM_001394603
NM_001394605
NM_001394608
NM_001394610
NM_001394613
NM_001394614
NM_001394615
NM_001394616
NM_001394617
NM_001394618
NM_001394619
NM_001394620
NM_001394621
NM_001394622
NM_001394623
NM_001394625
NM_001394626
NM_001394627
NM_001394628
NM_001394629
NM_001394630
NM_001394631

NM_001110850
NM_001110851
NM_001110852
NM_001110853
NM_001110854

NM_001110855
NM_001110856
NM_001110857
NM_001110858
NM_001110859
NM_001271503
NM_001271504
NM_001271505
NM_001271506
NM_013498
NM_001311066
NM_001311067
NM_001374833

RefSeq (protein)
NP_001254491
NP_001254492
NP_001254493
NP_001254494
NP_001254495

NP_001254496
NP_001254497
NP_001254498
NP_001254499
NP_001872
NP_853549
NP_874386
NP_874387
NP_874388
NP_874389
NP_874390
NP_874392
NP_874393
NP_877570
NP_877571
NP_877572
NP_877573
NP_898829
NP_898830
NP_898831
NP_898883
NP_001339374
NP_001339375
NP_001339394
NP_001339395
NP_001339396

NP_001104320
NP_001104321
NP_001104322
NP_001104323
NP_001104324

NP_001104325
NP_001104326
NP_001104327
NP_001104328
NP_001104329
NP_001258432
NP_001258433
NP_001258434
NP_001258435
NP_001297995
NP_001297996
NP_038526
NP_001361762

Location (UCSC)Chr 10: 35.13 – 35.21 MbChr 18: 3.27 – 3.34 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

cAMP responsive element modulator is a protein that in humans is encoded by the CREM gene,[5][6][7] and it belongs to the cAMP-responsive element binding protein family. It has multiple isoforms, which act either as repressors or activators.[8] CREB family is important for in regulating transcription in response to various stresses, metabolic and developmental signals.[9] CREM transcription factors also play an important role in many physiological systems, such as cardiac function,[10] circadian rhythms,[11] locomotion and spermatogenesis.[12]

Function

This gene encodes a bZIP transcription factor that binds to the cAMP responsive element found in many viral and cellular promoters. It is an important component of cAMP-mediated signal transduction during the spermatogenetic cycle, as well as other complex processes. Alternative promoter and translation initiation site usage allows this gene to exert spatial and temporal specificity to cAMP responsiveness. Multiple alternatively spliced transcript variants encoding several different isoforms have been found for this gene, with some of them functioning as activators and some as repressors of transcription.[7]

Gene location

The chromosomal location of CREM gene is at 10p11.21, where it starts at 35415769 and ends at 35501886 bp from pter ( according to hg19-Feb_2009)[13]

Interactions

CAMP responsive element modulator has been shown to interact with FHL5.[14][15]

Disease relevance of CREM

Panic disorder

One study reported the DNA sequence variations in the gene for CREM in panic disorder patients. It showed a significant excess of the shorter eight-repeat allele and of genotypes containing the eight-repeat allele in panic disorder patients.[16] The observed associations were limited to panic disorder without agoraphobia, and they were more prominent in females. But, the independent Italian and Spanish samples in this study did not support their results. Another family-based study showed little evidence of any susceptibility locus for panic disorder either within the CREM gene or in a nearby region on chromosome 10p11[17]

Spermiogenesis deficiency

CREM has been shown to be a master-switch regulator in testis.[18] It plays an important role in the regulation of the expression of post-meiotic genes, and this has been supported by several studies using CREM-mutation mice.[19] The results showed the first step in the process of sperm formation would be blocked if the germ cell development in mice CREM gene were disrupted. The cAMP response element sites can be found in the promoter region of some postmeiotic genes, so that the CREM can target and regulate these genes.[18]

Two studies proved that treat the rats with Salvia hypoleuca and Alpina galanga can significantly increased the CREM gene expression.[20][21]

Systemic lupus erythematousus

Less IL-2 will be produced from T cells in humans or mice with systemic lupus erythematousus (SLE). Some studies showed that an increased level CREM was presented in the nucleus of T lymphocytes from SLE patients. The CREM bound to the -180 site of the IL-2 promoter to repress its transcription.[22]

References

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000095794 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000063889 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Meyer TE, Habener JF (Nov 1992). "Cyclic AMP response element binding protein CREB and modulator protein CREM are products of distinct genes". Nucleic Acids Research. 20 (22): 6106. doi:10.1093/nar/20.22.6106. PMC 334485. PMID 1461747.
  6. ^ Masquilier D, Foulkes NS, Mattei MG, Sassone-Corsi P (Nov 1993). "Human CREM gene: evolutionary conservation, chromosomal localization, and inducibility of the transcript". Cell Growth & Differentiation. 4 (11): 931–7. PMID 7916662.
  7. ^ a b "Entrez Gene: CREM cAMP responsive element modulator".
  8. ^ Foulkes NS, Sassone-Corsi P (1992-02-07). "More is better: activators and repressors from the same gene". Cell. 68 (3): 411–414. doi:10.1016/0092-8674(92)90178-f. ISSN 0092-8674. PMID 1739963. S2CID 34290449.
  9. ^ Sassone-Corsi P (1995-01-01). "Transcription factors responsive to cAMP". Annual Review of Cell and Developmental Biology. 11: 355–377. doi:10.1146/annurev.cb.11.110195.002035. ISSN 1081-0706. PMID 8689562.
  10. ^ Isoda T, Paolocci N, Haghighi K, Wang C, Wang Y, Georgakopoulos D, Servillo G, Della Fazia MA, Kranias EG (2003-02-01). "Novel regulation of cardiac force-frequency relation by CREM (cAMP response element modulator)". FASEB Journal. 17 (2): 144–151. doi:10.1096/fj.01-0981com. ISSN 1530-6860. PMID 12554693. S2CID 17890025.
  11. ^ Sassone-Corsi P (2000-06-01). "CREM: a master-switch regulating the balance between differentiation and apoptosis in male germ cells". Molecular Reproduction and Development. 56 (2 Suppl): 228–229. doi:10.1002/(SICI)1098-2795(200006)56:2+<228::AID-MRD2>3.0.CO;2-B. ISSN 1040-452X. PMID 10824972. S2CID 21160055.
  12. ^ Sassone-Corsi P (1998-08-01). "CREM: a master-switch governing male germ cells differentiation and apoptosis". Seminars in Cell & Developmental Biology. 9 (4): 475–482. doi:10.1006/scdb.1998.0200. ISSN 1084-9521. PMID 9813195.
  13. ^ "CREM (cAMP responsive element modulator)". atlasgeneticsoncology.org. Retrieved 2016-10-16.
  14. ^ Fimia GM, De Cesare D, Sassone-Corsi P (Nov 2000). "A family of LIM-only transcriptional coactivators: tissue-specific expression and selective activation of CREB and CREM". Molecular and Cellular Biology. 20 (22): 8613–22. doi:10.1128/MCB.20.22.8613-8622.2000. PMC 102166. PMID 11046156.
  15. ^ Fimia GM, De Cesare D, Sassone-Corsi P (Mar 1999). "CBP-independent activation of CREM and CREB by the LIM-only protein ACT". Nature. 398 (6723): 165–9. Bibcode:1999Natur.398..165F. doi:10.1038/18237. PMID 10086359. S2CID 4424908.
  16. ^ Domschke K, Kuhlenbäumer G, Schirmacher A, Lorenzi C, Armengol L, DiBella D, Gratacos M, Garritsen HS, Nöthen MM (2003-02-01). "Human nuclear transcription factor gene CREM: genomic organization, mutation screening, and association analysis in panic disorder". American Journal of Medical Genetics Part B. 117B (1): 70–78. doi:10.1002/ajmg.b.10018. ISSN 1552-4841. PMID 12555239. S2CID 8884044.
  17. ^ Hamilton SP, Slager SL, Mayo D, Heiman GA, Klein DF, Hodge SE, Fyer AJ, Weissman MM, Knowles JA (2004-04-01). "Investigation of polymorphisms in the CREM gene in panic disorder". American Journal of Medical Genetics Part B. 126B (1): 111–115. doi:10.1002/ajmg.b.20121. ISSN 1552-4841. PMID 15048659. S2CID 43810849.
  18. ^ a b Krausz C, Sassone-Corsi P (2005-01-01). "Genetic control of spermiogenesis: insights from the CREM gene and implications for human infertility". Reproductive BioMedicine Online. 10 (1): 64–71. doi:10.1016/S1472-6483(10)60805-X. PMID 15705296.
  19. ^ Nantel F, Monaco L, Foulkes NS, Masquilier D, LeMeur M, Henriksén K, Dierich A, Parvinen M, Sassone-Corsi P (1996-03-14). "Spermiogenesis deficiency and germ-cell apoptosis in CREM-mutant mice". Nature. 380 (6570): 159–162. Bibcode:1996Natur.380..159N. doi:10.1038/380159a0. ISSN 0028-0836. PMID 8600390. S2CID 4278745.
  20. ^ Jasem E, Nasim J, Gholamreza M, Naser S, Nader M, Maryam SL, Abbas N, Vahid R (2010-10-01). "Evaluation of the effects of Salvia hypoleuca on the cAMP-responsive element modulator (CREM) gene expression and spermatogenesis in rat". Middle East Fertility Society Journal. 15 (4): 274–277. doi:10.1016/j.mefs.2010.08.002.
  21. ^ Mazaheri M, Shahdadi V, Nazari Boron A (2016-10-16). "Molecullar and biochemical effect of alcoholic extract of Alpinia galanga on rat spermatogenesis process". Iranian Journal of Reproductive Medicine. 12 (11): 765–770. ISSN 1680-6433. PMC 4330656. PMID 25709632.
  22. ^ Juang YT, Wang Y, Solomou EE, Li Y, Mawrin C, Tenbrock K, Kyttaris VC, Tsokos GC (2005-04-01). "Systemic lupus erythematosus serum IgG increases CREM binding to the IL-2 promoter and suppresses IL-2 production through CaMKIV". Journal of Clinical Investigation. 115 (4): 996–1005. doi:10.1172/JCI22854. ISSN 0021-9738. PMC 1070410. PMID 15841182.

Further reading

  • Don J, Stelzer G (Feb 2002). "The expanding family of CREB/CREM transcription factors that are involved with spermatogenesis". Molecular and Cellular Endocrinology. 187 (1–2): 115–24. doi:10.1016/S0303-7207(01)00696-7. PMID 11988318. S2CID 23023082.
  • Yan C, Miller CL, Abe J (Mar 2007). "Regulation of phosphodiesterase 3 and inducible cAMP early repressor in the heart". Circulation Research. 100 (4): 489–501. doi:10.1161/01.RES.0000258451.44949.d7. PMC 4115784. PMID 17332439.
  • Pongubala JM, Atchison ML (Apr 1995). "Activating transcription factor 1 and cyclic AMP response element modulator can modulate the activity of the immunoglobulin kappa 3' enhancer". The Journal of Biological Chemistry. 270 (17): 10304–13. doi:10.1074/jbc.270.17.10304. PMID 7730336.
  • Walker WH, Sanborn BM, Habener JF (Dec 1994). "An isoform of transcription factor CREM expressed during spermatogenesis lacks the phosphorylation domain and represses cAMP-induced transcription". Proceedings of the National Academy of Sciences of the United States of America. 91 (26): 12423–7. Bibcode:1994PNAS...9112423W. doi:10.1073/pnas.91.26.12423. PMC 45450. PMID 7809053.
  • Fujimoto T, Fujisawa J, Yoshida M (Feb 1994). "Novel isoforms of human cyclic AMP-responsive element modulator (hCREM) mRNA". Journal of Biochemistry. 115 (2): 298–303. doi:10.1093/oxfordjournals.jbchem.a124332. PMID 8206879.
  • de Groot RP, den Hertog J, Vandenheede JR, Goris J, Sassone-Corsi P (Oct 1993). "Multiple and cooperative phosphorylation events regulate the CREM activator function". The EMBO Journal. 12 (10): 3903–11. doi:10.1002/j.1460-2075.1993.tb06068.x. PMC 413673. PMID 8404858.
  • Bodor J, Walker W, Flemington E, Spetz AL, Habener JF (Dec 1995). "Modulation of Tax and PKA-mediated expression of HTLV-I promoter via cAMP response element binding and modulator proteins CREB and CREM". FEBS Letters. 377 (3): 413–8. doi:10.1016/0014-5793(95)01299-0. PMID 8549766. S2CID 45422227.
  • Nantel F, Monaco L, Foulkes NS, Masquilier D, LeMeur M, Henriksén K, Dierich A, Parvinen M, Sassone-Corsi P (Mar 1996). "Spermiogenesis deficiency and germ-cell apoptosis in CREM-mutant mice". Nature. 380 (6570): 159–62. Bibcode:1996Natur.380..159N. doi:10.1038/380159a0. PMID 8600390. S2CID 4278745.
  • Blendy JA, Kaestner KH, Weinbauer GF, Nieschlag E, Schütz G (Mar 1996). "Severe impairment of spermatogenesis in mice lacking the CREM gene". Nature. 380 (6570): 162–5. Bibcode:1996Natur.380..162B. doi:10.1038/380162a0. PMID 8600391. S2CID 4337719.
  • Bodor J, Spetz AL, Strominger JL, Habener JF (Apr 1996). "cAMP inducibility of transcriptional repressor ICER in developing and mature human T lymphocytes". Proceedings of the National Academy of Sciences of the United States of America. 93 (8): 3536–41. Bibcode:1996PNAS...93.3536B. doi:10.1073/pnas.93.8.3536. PMC 39645. PMID 8622971.
  • Gellersen B, Kempf R, Telgmann R (Jan 1997). "Human endometrial stromal cells express novel isoforms of the transcriptional modulator CREM and up-regulate ICER in the course of decidualization". Molecular Endocrinology. 11 (1): 97–113. doi:10.1210/mend.11.1.9875. PMID 8994192.
  • Laurance ME, Kwok RP, Huang MS, Richards JP, Lundblad JR, Goodman RH (Jan 1997). "Differential activation of viral and cellular promoters by human T-cell lymphotropic virus-1 tax and cAMP-responsive element modulator isoforms". The Journal of Biological Chemistry. 272 (5): 2646–51. doi:10.1074/jbc.272.5.2646. PMID 9006899.
  • Bonny C, Cooker LA, Goldberg E (Mar 1998). "Deoxyribonucleic acid-protein interactions and expression of the human testis-specific lactate dehydrogenase promoter: transcription factor Sp1 plays a major role". Biology of Reproduction. 58 (3): 754–9. doi:10.1095/biolreprod58.3.754. PMID 9510963.
  • Müller FU, Bokník P, Knapp J, Neumann J, Vahlensieck U, Oetjen E, Scheld HH, Schmitz W (Sep 1998). "Identification and expression of a novel isoform of cAMP response element modulator in the human heart". FASEB Journal. 12 (12): 1191–9. doi:10.1096/fasebj.12.12.1191. PMID 9737722. S2CID 34554530.
  • Fimia GM, De Cesare D, Sassone-Corsi P (Mar 1999). "CBP-independent activation of CREM and CREB by the LIM-only protein ACT". Nature. 398 (6723): 165–9. Bibcode:1999Natur.398..165F. doi:10.1038/18237. PMID 10086359. S2CID 4424908.
  • Pati D, Meistrich ML, Plon SE (Jul 1999). "Human Cdc34 and Rad6B ubiquitin-conjugating enzymes target repressors of cyclic AMP-induced transcription for proteolysis". Molecular and Cellular Biology. 19 (7): 5001–13. doi:10.1128/mcb.19.7.5001. PMC 84326. PMID 10373550.
  • Inada A, Someya Y, Yamada Y, Ihara Y, Kubota A, Ban N, Watanabe R, Tsuda K, Seino Y (Jul 1999). "The cyclic AMP response element modulator family regulates the insulin gene transcription by interacting with transcription factor IID". The Journal of Biological Chemistry. 274 (30): 21095–103. doi:10.1074/jbc.274.30.21095. PMID 10409662.
  • Zauli G, Secchiero P, Rodella L, Gibellini D, Mirandola P, Mazzoni M, Milani D, Dowd DR, Capitani S, Vitale M (Feb 2000). "HIV-1 Tat-mediated inhibition of the tyrosine hydroxylase gene expression in dopaminergic neuronal cells". The Journal of Biological Chemistry. 275 (6): 4159–65. doi:10.1074/jbc.275.6.4159. PMID 10660577.

External links

  • v
  • t
  • e
  • 1dh3: CRYSTAL STRUCTURE OF A CREB BZIP-CRE COMPLEX REVEALS THE BASIS FOR CREB FAIMLY SELECTIVE DIMERIZATION AND DNA BINDING
    1dh3: CRYSTAL STRUCTURE OF A CREB BZIP-CRE COMPLEX REVEALS THE BASIS FOR CREB FAIMLY SELECTIVE DIMERIZATION AND DNA BINDING
  • v
  • t
  • e
(1) Basic domains
(1.1) Basic leucine zipper (bZIP)
(1.2) Basic helix-loop-helix (bHLH)
Group A
Group B
Group C
bHLH-PAS
Group D
Group E
Group F
bHLH-COE
(1.3) bHLH-ZIP
(1.4) NF-1
(1.5) RF-X
(1.6) Basic helix-span-helix (bHSH)
(2) Zinc finger DNA-binding domains
(2.1) Nuclear receptor (Cys4)
subfamily 1
subfamily 2
subfamily 3
subfamily 4
subfamily 5
subfamily 6
subfamily 0
(2.2) Other Cys4
(2.3) Cys2His2
(2.4) Cys6
(2.5) Alternating composition
(2.6) WRKY
(3) Helix-turn-helix domains
(3.1) Homeodomain
Antennapedia
ANTP class
protoHOX
Hox-like
metaHOX
NK-like
other
(3.2) Paired box
(3.3) Fork head / winged helix
(3.4) Heat shock factors
(3.5) Tryptophan clusters
(3.6) TEA domain
  • transcriptional enhancer factor
(4) β-Scaffold factors with minor groove contacts
(4.1) Rel homology region
(4.2) STAT
(4.3) p53-like
(4.4) MADS box
(4.6) TATA-binding proteins
(4.7) High-mobility group
(4.9) Grainyhead
(4.10) Cold-shock domain
(4.11) Runt
(0) Other transcription factors
(0.2) HMGI(Y)
(0.3) Pocket domain
(0.5) AP-2/EREBP-related factors
(0.6) Miscellaneous
see also transcription factor/coregulator deficiencies

This article incorporates text from the United States National Library of Medicine, which is in the public domain.