개연성 돌리칠 피로인산염 Glc1Man9GlcNAc2 알파-1,3-glucosyl transferase는 인간에서 ALG8 유전자 에 의해 암호화된 효소 다.[5]
이 유전자는 ALG6/ALG8 글루코실트전달효소 계열의 한 구성원을 인코딩한다. 인코딩된 단백질은 단백질의 N연계 글리코실화를 위해 지질연계 올리고당 전구체에 두 번째 포도당 잔류물을 추가하는 촉매 작용을 한다. 이 유전자의 돌연변이는 글리코실레이션 타입 Ih(CDG-Ih)의 선천성 질환과 관련이 있다. 대안으로 서로 다른 ISO 양식을 인코딩하는 분할된 대본 변형이 식별되었다.[5]
참조 추가 읽기 Jaeken J (2005). "Congenital disorders of glycosylation (CDG): update and new developments". J. Inherit. Metab. Dis . 27 (3): 423–6. doi :10.1023/B:BOLI.0000031221.44647.9e . PMID 15272470 . S2CID 7608163 . Jaeken J, Carchon H (2004). "Congenital disorders of glycosylation: a booming chapter of pediatrics". Curr. Opin. Pediatr . 16 (4): 434–9. doi :10.1097/01.mop.0000133636.56790.4a . PMID 15273506 . Adams MD, Kerlavage AR, Fleischmann RD, et al. (1995). "Initial assessment of human gene diversity and expression patterns based upon 83 million nucleotides of cDNA sequence" (PDF) . Nature . 377 (6547 Suppl): 3–174. PMID 7566098 . Stanchi F, Bertocco E, Toppo S, et al. (2001). "Characterization of 16 novel human genes showing high similarity to yeast sequences". Yeast . 18 (1): 69–80. doi :10.1002/1097-0061(200101)18:1<69::AID-YEA647>3.0.CO;2-H . PMID 11124703 . Oriol R, Martinez-Duncker I, Chantret I, et al. (2003). "Common origin and evolution of glycosyltransferases using Dol-P-monosaccharides as donor substrate". Mol. Biol. Evol . 19 (9): 1451–63. doi :10.1093/oxfordjournals.molbev.a004208 . PMID 12200473 . 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): 16899–903. doi :10.1073/pnas.242603899 . PMC 139241 . PMID 12477932 . Chantret I, Dancourt J, Dupré T, et al. (2003). "A deficiency in dolichyl-P-glucose:Glc1Man9GlcNAc2-PP-dolichyl alpha3-glucosyltransferase defines a new subtype of congenital disorders of glycosylation" . J. Biol. Chem . 278 (11): 9962–71. doi :10.1074/jbc.M211950200 . PMID 12480927 . Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs" . Nat. Genet . 36 (1): 40–5. doi :10.1038/ng1285 . PMID 14702039 . Schollen E, Frank CG, Keldermans L, et al. (2004). "Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih (CDG-Ih) (ALG8 deficiency)" . J. Med. Genet . 41 (7): 550–6. doi :10.1136/jmg.2003.016923 . PMC 1735831 . PMID 15235028 . 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): 2121–7. doi :10.1101/gr.2596504 . PMC 528928 . PMID 15489334 . Otsuki T, Ota T, Nishikawa T, et al. (2007). "Signal sequence and keyword trap in silico for selection of full-length human cDNAs encoding secretion or membrane proteins from oligo-capped cDNA libraries" . DNA Res . 12 (2): 117–26. doi :10.1093/dnares/12.2.117 . PMID 16303743 . Kimura K, Wakamatsu A, Suzuki Y, et al. (2006). "Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes" . Genome Res . 16 (1): 55–65. doi :10.1101/gr.4039406 . PMC 1356129 . PMID 16344560 .
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