RTN1

RTN1
RTN1
식별자
에일리어스RTN1, NSP, 레티큘론 1
외부 IDOMIM : 6008655 MGI : 1933947 HomoloGene : 49654 GenCard : RTN1
맞춤법
종.인간마우스
엔트레즈

6252

104001

앙상블

ENSG00000139970

ENSMUSG000021087

유니프로트

문제 16799

Q8K0T0

RefSeq(mRNA)

NM_001243115
NM_021136
NM_206852
NM_206857
NM_001363702

NM_001007596
NM_001286448
NM_153457

RefSeq(단백질)

NP_066959
NP_996734
NP_001350631

NP_001007597
NP_001273377
NP_703187

장소(UCSC)Chr 14: 59.6 ~59.87 MbChr 12: 72.26 ~72.46 Mb
PubMed 검색[3][4]
위키데이터
인간 보기/편집마우스 표시/편집

신경내분비특이단백질(NSP)로도 알려진 레티큘론-1은 RTN1 [5][6]유전자에 의해 인간에게 암호화되는 단백질이다.

이 유전자는 망상암호화유전자군에 속한다.망막은 내소체와 관련지어 신경내분비 분비 또는 신경내분비세포의 막트래픽에 관여한다.다른 아이소폼을 코드하는 대체적으로 스플라이스된 전사 변종이 식별되었다.이러한 [6]다양성에는 내부 exon의 대체 스플라이싱보다는 여러 프로모터가 관여하는 것으로 보입니다.

상호 작용

RTN1은 BCL2와 같은1[7] 및 UGCG와 [8]상호작용하는 것으로 나타났습니다.

레퍼런스

  1. ^ a b c GRCh38: 앙상블 릴리즈 89: ENSG00000139970 - 앙상블, 2017년 5월
  2. ^ a b c GRCm38: 앙상블 릴리즈 89: ENSMUSG000021087 - 앙상블, 2017년 5월
  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. ^ Kools PF, Roebroek AJ, Van de Velde HJ, Marynen P, Bullerdiek J, Van de Ven WJ (February 1994). "Regional mapping of the human NSP gene to chromosome region 14q21→q22 by fluorescence in situ hybridization analysis". Cytogenet Cell Genet. 66 (1): 48–50. doi:10.1159/000133662. PMID 8275708.
  6. ^ a b "Entrez Gene: RTN1 reticulon 1".
  7. ^ Tagami S, Eguchi Y, Kinoshita M, Takeda M, Tsujimoto Y (November 2000). "A novel protein, RTN-XS, interacts with both Bcl-XL and Bcl-2 on endoplasmic reticulum and reduces their anti-apoptotic activity". Oncogene. 19 (50): 5736–46. doi:10.1038/sj.onc.1203948. PMID 11126360.
  8. ^ Di Sano F, Fazi B, Citro G, Lovat PE, Cesareni G, Piacentini M (July 2003). "Glucosylceramide synthase and its functional interaction with RTN-1C regulate chemotherapeutic-induced apoptosis in neuroepithelioma cells". Cancer Res. 63 (14): 3860–5. PMID 12873973.

추가 정보

  • Senden NH, van de Velde HJ, Broers JL, Timmer ED, Roebroek AJ, van de Ven WJ, Ramaekers FC (1994). "Cluster-10 lung-cancer antibodies recognize NSPs, novel neuro-endocrine proteins associated with membranes of the endoplasmic reticulum". Int. J. Cancer Suppl. 8: 84–8. doi:10.1002/ijc.2910570718. PMID 7515034.
  • Roebroek AJ, van de Velde HJ, Van Bokhoven A, Broers JL, Ramaekers FC, Van de Ven WJ (1993). "Cloning and expression of alternative transcripts of a novel neuroendocrine-specific gene and identification of its 135-kDa translational product". J. Biol. Chem. 268 (18): 13439–47. PMID 7685762.
  • van de Velde HJ, Roebroek AJ, Senden NH, Ramaekers FC, Van de Ven WJ (1995). "NSP-encoded reticulons, neuroendocrine proteins of a novel gene family associated with membranes of the endoplasmic reticulum". J. Cell Sci. 107 (9): 2403–16. PMID 7844160.
  • van de Velde HJ, Senden NH, Roskams TA, Broers JL, Ramaekers FC, Roebroek AJ, Van de Ven WJ (1994). "NSP-encoded reticulons are neuroendocrine markers of a novel category in human lung cancer diagnosis". Cancer Res. 54 (17): 4769–76. PMID 8062278.
  • Roebroek AJ, Ayoubi TA, Van de Velde HJ, Schoenmakers EF, Pauli IG, Van de Ven WJ (1997). "Genomic organization of the human NSP gene, prototype of a novel gene family encoding reticulons". Genomics. 32 (2): 191–9. doi:10.1006/geno.1996.0105. PMID 8833145.
  • Bonaldo MF, Lennon G, Soares MB (1997). "Normalization and subtraction: two approaches to facilitate gene discovery". Genome Res. 6 (9): 791–806. doi:10.1101/gr.6.9.791. PMID 8889548.
  • Senden NH, Timmer ED, Boers JE, van de Velde HJ, Roebroek AJ, Van de Ven WJ, Broers JL, Ramaekers FC (1996). "Neuroendocrine-specific protein C (NSP-C): subcellular localization and differential expression in relation to NSP-A". Eur. J. Cell Biol. 69 (3): 197–213. PMID 8900485.
  • Hens J, Nuydens R, Geerts H, Senden NH, Van de Ven WJ, Roebroek AJ, van de Velde HJ, Ramaekers FC, Broers JL (1998). "Neuronal differentiation is accompanied by NSP-C expression". Cell Tissue Res. 292 (2): 229–37. doi:10.1007/s004410051054. PMID 9560466.
  • Tagami S, Eguchi Y, Kinoshita M, Takeda M, Tsujimoto Y (2001). "A novel protein, RTN-XS, interacts with both Bcl-XL and Bcl-2 on endoplasmic reticulum and reduces their anti-apoptotic activity". Oncogene. 19 (50): 5736–46. doi:10.1038/sj.onc.1203948. PMID 11126360.
  • Oertle T, Klinger M, Stuermer CA, Schwab ME (2003). "A reticular rhapsody: phylogenic evolution and nomenclature of the RTN/Nogo gene family". FASEB J. 17 (10): 1238–47. CiteSeerX 10.1.1.124.969. doi:10.1096/fj.02-1166hyp. PMID 12832288.
  • Di Sano F, Fazi B, Citro G, Lovat PE, Cesareni G, Piacentini M (2003). "Glucosylceramide synthase and its functional interaction with RTN-1C regulate chemotherapeutic-induced apoptosis in neuroepithelioma cells". Cancer Res. 63 (14): 3860–5. PMID 12873973.
  • Iwahashi J, Hamada N (2004). "Human reticulon 1-A and 1-B interact with a medium chain of the AP-2 adaptor complex". Cell. Mol. Biol. (Noisy-le-grand). 49 Online Pub: OL467–71. PMID 14995077.
  • Hu Y, Fang X, Dunham SM, Prada C, Stachowiak EK, Stachowiak MK (2004). "90-kDa ribosomal S6 kinase is a direct target for the nuclear fibroblast growth factor receptor 1 (FGFR1): role in FGFR1 signaling". J. Biol. Chem. 279 (28): 29325–35. doi:10.1074/jbc.M311144200. PMID 15117958.
  • He W, Lu Y, Qahwash I, Hu XY, Chang A, Yan R (2004). "Reticulon family members modulate BACE1 activity and amyloid-beta peptide generation". Nat. Med. 10 (9): 959–65. doi:10.1038/nm1088. PMID 15286784.
  • Rual JF, Venkatesan K, Hao T, Hirozane-Kishikawa T, Dricot A, Li N, Berriz GF, Gibbons FD, Dreze M, Ayivi-Guedehoussou N, Klitgord N, Simon C, Boxem M, Milstein S, Rosenberg J, Goldberg DS, Zhang LV, Wong SL, Franklin G, Li S, Albala JS, Lim J, Fraughton C, Llamosas E, Cevik S, Bex C, Lamesch P, Sikorski RS, Vandenhaute J, Zoghbi HY, Smolyar A, Bosak S, Sequerra R, Doucette-Stamm L, Cusick ME, Hill DE, Roth FP, Vidal M (2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. doi:10.1038/nature04209. PMID 16189514.
  • Mannan AU, Boehm J, Sauter SM, Rauber A, Byrne PC, Neesen J, Engel W (2007). "Spastin, the most commonly mutated protein in hereditary spastic paraplegia interacts with Reticulon 1 an endoplasmic reticulum protein". Neurogenetics. 7 (2): 93–103. doi:10.1007/s10048-006-0034-4. PMID 16602018.


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인간 염색체 14번 유전자에 대한 이 기사는 짧은 글이다.위키피디아를 확장함으로써 위키피디아를 도울 수 있습니다.