MBNL1

MBNL1
Available structures
PDB	Ortholog search: PDBe RCSB
List of PDB id codes
	3D2N, 3D2Q, 3D2S
Identifiers
Aliases	MBNL1, EXP, EXP35, EXP40, EXP42, MBNL, muscleblind like splicing regulator 1
External IDs	MGI: 1928482 HomoloGene: 23186 GeneCards: MBNL1
Gene location (Human)
Chr.	Chromosome 3 (human)[1]
End	152,465,780 bp[1]
Gene location (Mouse)
Chr.	Chromosome 3 (mouse)[2]
End	60,629,750 bp[2]
RNA expression pattern
	; ; ; ;
	More reference expression data
Gene ontology
Molecular function	• regulatory region RNA binding; • double-stranded RNA binding; • protein binding; • metal ion binding; • RNA binding;
Cellular component	• cytoplasm; • centrosome; • cytoplasmic stress granule; • cell nucleus; • nucleoplasm; • cytosol;
Biological process	• mRNA processing; • regulation of RNA splicing; • myoblast differentiation; • in utero embryonic development; • embryonic limb morphogenesis; • RNA splicing; • nervous system development;
	Sources:Amigo / QuickGO
Orthologs
	4154
	56758
	ENSG00000152601
	ENSMUSG00000027763
	Q9NR56; Q86VM6
	Q9JKP5
NM_001314057; NM_021038; NM_207292; NM_207293; NM_207294;
	NM_207295; NM_207296; NM_207297; NM_001363870
NM_001253708; NM_001253709; NM_001253710; NM_001253711; NM_001253713;
	NM_020007; NM_001310514
NP_001300986; NP_066368; NP_997175; NP_997176; NP_997177;
	NP_997178; NP_997179; NP_997180; NP_001350799; NP_001300986.1; NP_997178.1; NP_997179.1; NP_997180.1
NP_001240637; NP_001240638; NP_001240639; NP_001240640; NP_001240642;
	NP_001297443; NP_064391
	Wikidata
View/Edit Human	View/Edit Mouse

Muscleblind-like (Drosophila), also known as MBNL1, is a protein that in humans is encoded by the MBNL1 gene.^[5]^[6]^[7] It has been implicated in Myotonic dystrophy and has been shown to autoregulate its transcript.^[8]

References

1 2 3 GRCh38: Ensembl release 89: ENSG00000152601 - Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000027763 - Ensembl, May 2017
↑ "Human PubMed Reference:".
↑ "Mouse PubMed Reference:".
↑ Ishikawa K, Nagase T, Nakajima D, Seki N, Ohira M, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O (Oct 1997). "Prediction of the coding sequences of unidentified human genes. VIII. 78 new cDNA clones from brain which code for large proteins in vitro". DNA Research. 4 (5): 307–13. doi:10.1093/dnares/4.5.307. PMID 9455477.
↑ Miller JW, Urbinati CR, Teng-Umnuay P, Stenberg MG, Byrne BJ, Thornton CA, Swanson MS (Sep 2000). "Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy". The EMBO Journal. 19 (17): 4439–48. doi:10.1093/emboj/19.17.4439. PMC 302046. PMID 10970838.
↑ "Entrez Gene: MBNL1 muscleblind-like (Drosophila)".
↑ Ho TH, Charlet-B N, Poulos MG, Singh G, Swanson MS, Cooper TA (Aug 2004). "Muscleblind proteins regulate alternative splicing". The EMBO Journal. 23 (15): 3103–12. doi:10.1038/sj.emboj.7600300. PMC 514918. PMID 15257297.

Bonaldo MF, Lennon G, Soares MB (Sep 1996). "Normalization and subtraction: two approaches to facilitate gene discovery". Genome Research. 6 (9): 791–806. doi:10.1101/gr.6.9.791. PMID 8889548.
Fardaei M, Larkin K, Brook JD, Hamshere MG (Jul 2001). "In vivo co-localisation of MBNL protein with DMPK expanded-repeat transcripts". Nucleic Acids Research. 29 (13): 2766–71. doi:10.1093/nar/29.13.2766. PMC 55763. PMID 11433021.
Mankodi A, Urbinati CR, Yuan QP, Moxley RT, Sansone V, Krym M, Henderson D, Schalling M, Swanson MS, Thornton CA (Sep 2001). "Muscleblind localizes to nuclear foci of aberrant RNA in myotonic dystrophy types 1 and 2" (PDF). Human Molecular Genetics. 10 (19): 2165–70. doi:10.1093/hmg/10.19.2165. PMID 11590133.
Fardaei M, Rogers MT, Thorpe HM, Larkin K, Hamshere MG, Harper PS, Brook JD (Apr 2002). "Three proteins, MBNL, MBLL and MBXL, co-localize in vivo with nuclear foci of expanded-repeat transcripts in DM1 and DM2 cells". Human Molecular Genetics. 11 (7): 805–14. doi:10.1093/hmg/11.7.805. PMID 11929853.
Kino Y, Mori D, Oma Y, Takeshita Y, Sasagawa N, Ishiura S (Mar 2004). "Muscleblind protein, MBNL1/EXP, binds specifically to CHHG repeats". Human Molecular Genetics. 13 (5): 495–507. CiteSeerX 10.1.1.598.7921. doi:10.1093/hmg/ddh056. PMID 14722159.
Dansithong W, Paul S, Comai L, Reddy S (Feb 2005). "MBNL1 is the primary determinant of focus formation and aberrant insulin receptor splicing in DM1". The Journal of Biological Chemistry. 280 (7): 5773–80. doi:10.1074/jbc.M410781200. PMID 15546872.
Ho TH, Savkur RS, Poulos MG, Mancini MA, Swanson MS, Cooper TA (Jul 2005). "Colocalization of muscleblind with RNA foci is separable from mis-regulation of alternative splicing in myotonic dystrophy". Journal of Cell Science. 118 (Pt 13): 2923–33. doi:10.1242/jcs.02404. PMID 15961406.
Adereth Y, Dammai V, Kose N, Li R, Hsu T (Dec 2005). "RNA-dependent integrin alpha3 protein localization regulated by the Muscleblind-like protein MLP1". Nature Cell Biology. 7 (12): 1240–7. doi:10.1038/ncb1335. PMC 2365307. PMID 16273094.
Monferrer L, Artero R (2006). "An interspecific functional complementation test in Drosophila for introductory genetics laboratory courses". The Journal of Heredity. 97 (1): 67–73. doi:10.1093/jhered/esj003. PMID 16394256.
Cardani R, Mancinelli E, Rotondo G, Sansone V, Meola G (2007). "Muscleblind-like protein 1 nuclear sequestration is a molecular pathology marker of DM1 and DM2". European Journal of Histochemistry. 50 (3): 177–82. PMID 16920640.
Paul S, Dansithong W, Kim D, Rossi J, Webster NJ, Comai L, Reddy S (Sep 2006). "Interaction of muscleblind, CUG-BP1 and hnRNP H proteins in DM1-associated aberrant IR splicing". The EMBO Journal. 25 (18): 4271–83. CiteSeerX 10.1.1.673.6397. doi:10.1038/sj.emboj.7601296. PMC 1570429. PMID 16946708.
Smith KP, Byron M, Johnson C, Xing Y, Lawrence JB (Sep 2007). "Defining early steps in mRNA transport: mutant mRNA in myotonic dystrophy type I is blocked at entry into SC-35 domains". The Journal of Cell Biology. 178 (6): 951–64. doi:10.1083/jcb.200706048. PMC 2064620. PMID 17846170.

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[refGRCh38Ensembl-1] 1 2 3 GRCh38: Ensembl release 89: ENSG00000152601 - Ensembl, May 2017

[refGRCm38Ensembl-2] 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000027763 - Ensembl, May 2017

[3] "Human PubMed Reference:".

[4] "Mouse PubMed Reference:".

[pmid9455477-5] Ishikawa K, Nagase T, Nakajima D, Seki N, Ohira M, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O (Oct 1997). "Prediction of the coding sequences of unidentified human genes. VIII. 78 new cDNA clones from brain which code for large proteins in vitro". DNA Research. 4 (5): 307–13. doi:10.1093/dnares/4.5.307. PMID 9455477.

[pmid10970838-6] Miller JW, Urbinati CR, Teng-Umnuay P, Stenberg MG, Byrne BJ, Thornton CA, Swanson MS (Sep 2000). "Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy". The EMBO Journal. 19 (17): 4439–48. doi:10.1093/emboj/19.17.4439. PMC 302046. PMID 10970838.

[entrez-7] "Entrez Gene: MBNL1 muscleblind-like (Drosophila)".

[pmid15257297-8] Ho TH, Charlet-B N, Poulos MG, Singh G, Swanson MS, Cooper TA (Aug 2004). "Muscleblind proteins regulate alternative splicing". The EMBO Journal. 23 (15): 3103–12. doi:10.1038/sj.emboj.7600300. PMC 514918. PMID 15257297.

MBNL1

References

Further reading