The protein encoded by this gene belongs to the ERG4/ERG24 family. It localizes to the inner membrane of the nuclear envelope and anchors the lamina and the heterochromatin to the membrane. It may mediate the interaction between chromatin and lamin B. Mutations of this gene has been associated with autosomal recessive HEM/Greenberg skeletal dysplasia. Alternative splicing occurs at this locus and two transcript variants encoding the same protein have been identified.[3]
↑Schuler E, Lin F, Worman HJ (April 1994). "Characterization of the human gene encoding LBR, an integral protein of the nuclear envelope inner membrane". The Journal of Biological Chemistry. 269 (15): 11312–7. PMID8157663.
↑Holmer L, Pezhman A, Worman HJ (December 1998). "The human lamin B receptor/sterol reductase multigene family". Genomics. 54 (3): 469–76. doi:10.1006/geno.1998.5615. PMID9878250.
↑ 6.06.1Ye Q, Worman HJ (June 1996). "Interaction between an integral protein of the nuclear envelope inner membrane and human chromodomain proteins homologous to Drosophila HP1". The Journal of Biological Chemistry. 271 (25): 14653–6. doi:10.1074/jbc.271.25.14653. PMID8663349.
↑Chen CK, Blanco M, Jackson C, Aznauryan E, Ollikainen N, Surka C, Chow A, Cerase A, McDonel P, Guttman M (October 2016). "Xist recruits the X chromosome to the nuclear lamina to enable chromosome-wide silencing". Science. 354 (6311): 468–472. doi:10.1126/science.aae0047. PMID27492478.
Maruyama K, Sugano S (January 1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID8125298.
Ye Q, Worman HJ (April 1994). "Primary structure analysis and lamin B and DNA binding of human LBR, an integral protein of the nuclear envelope inner membrane". The Journal of Biological Chemistry. 269 (15): 11306–11. PMID8157662.
Ye Q, Worman HJ (June 1996). "Interaction between an integral protein of the nuclear envelope inner membrane and human chromodomain proteins homologous to Drosophila HP1". The Journal of Biological Chemistry. 271 (25): 14653–6. doi:10.1074/jbc.271.25.14653. PMID8663349.
Wydner KL, McNeil JA, Lin F, Worman HJ, Lawrence JB (March 1996). "Chromosomal assignment of human nuclear envelope protein genes LMNA, LMNB1, and LBR by fluorescence in situ hybridization". Genomics. 32 (3): 474–8. doi:10.1006/geno.1996.0146. PMID8838815.
Ye Q, Callebaut I, Pezhman A, Courvalin JC, Worman HJ (June 1997). "Domain-specific interactions of human HP1-type chromodomain proteins and inner nuclear membrane protein LBR". The Journal of Biological Chemistry. 272 (23): 14983–9. doi:10.1074/jbc.272.23.14983. PMID9169472.
Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, Suyama A, Sugano S (October 1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID9373149.
Papoutsopoulou S, Nikolakaki E, Giannakouros T (February 1999). "SRPK1 and LBR protein kinases show identical substrate specificities". Biochemical and Biophysical Research Communications. 255 (3): 602–7. doi:10.1006/bbrc.1999.0249. PMID10049757.
Bedford MT, Sarbassova D, Xu J, Leder P, Yaffe MB (April 2000). "A novel pro-Arg motif recognized by WW domains". The Journal of Biological Chemistry. 275 (14): 10359–69. doi:10.1074/jbc.275.14.10359. PMID10744724.
Duband-Goulet I, Courvalin JC (May 2000). "Inner nuclear membrane protein LBR preferentially interacts with DNA secondary structures and nucleosomal linker". Biochemistry. 39 (21): 6483–8. doi:10.1021/bi992908b. PMID10828963.
Martins SB, Eide T, Steen RL, Jahnsen T, Skålhegg BS, Collas P (November 2000). "HA95 is a protein of the chromatin and nuclear matrix regulating nuclear envelope dynamics". Journal of Cell Science. 113 Pt 21: 3703–13. PMID11034899.
Takano M, Takeuchi M, Ito H, Furukawa K, Sugimoto K, Omata S, Horigome T (February 2002). "The binding of lamin B receptor to chromatin is regulated by phosphorylation in the RS region". European Journal of Biochemistry. 269 (3): 943–53. doi:10.1046/j.0014-2956.2001.02730.x. PMID11846796.
Hoffmann K, Dreger CK, Olins AL, Olins DE, Shultz LD, Lucke B, Karl H, Kaps R, Müller D, Vayá A, Aznar J, Ware RE, Sotelo Cruz N, Lindner TH, Herrmann H, Reis A, Sperling K (August 2002). "Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger-Huët anomaly)". Nature Genetics. 31 (4): 410–4. doi:10.1038/ng925. PMID12118250.
Wells L, Vosseller K, Cole RN, Cronshaw JM, Matunis MJ, Hart GW (October 2002). "Mapping sites of O-GlcNAc modification using affinity tags for serine and threonine post-translational modifications". Molecular & Cellular Proteomics. 1 (10): 791–804. doi:10.1074/mcp.M200048-MCP200. PMID12438562.