Identification of FAM96B as a novel prelamin A binding partner

Biochemical and Biophysical Research Communications

Volumn 440, Issue 1, 2013, Pages 20-24

  Xiong, Xing Dong ^a,b   Wang, Junwen ^a,b   Zheng, Huiling ^a,b   Jing, Xia ^a,b   Liu, Zhenjie ^a,b   Zhou, Zhongjun ^a,c   Liu, Xinguang ^a,b  

^a GUANGDONG MEDICAL UNIVERSITY   (China)

^b Key Laboratory for Medical Molecular Diagnostics of Guangdong Province   (China)

^c UNIVERSITY OF HONG KONG   (Hong Kong)

Author keywords

Cellular senescence; CIA; FAM96B; HGPS; Prelamin A

Indexed keywords

CELL PROTEIN; COMPLEMENTARY DNA; FAM96B PROTEIN; HYBRID PROTEIN; PRELAMIN A; UNCLASSIFIED DRUG;

ARTICLE; CELL AGING; CELL STRAIN HEK293; CELLULAR DISTRIBUTION; CONFOCAL MICROSCOPY; CONTROLLED STUDY; DNA LIBRARY; GENE SEQUENCE; HUMAN; HUMAN CELL; IMMUNOPRECIPITATION; PREMATURE AGING; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN BINDING; PROTEIN INTERACTION; PROTEIN LOCALIZATION; SENESCENCE; SKELETAL MUSCLE; TWO HYBRID SYSTEM; WESTERN BLOTTING;

CELLULAR SENESCENCE; CIA; FAM96B; FAMILY WITH SEQUENCE SIMILARITY 96 MEMBER B; HGPS; HUTCHINSON-GILFORD PROGERIA SYNDROME; PRELAMIN A; THE CYTOPLASMIC FE-S ASSEMBLY;

CARRIER PROTEINS; CELL AGING; HEK293 CELLS; HUMANS; NUCLEAR PROTEINS; PROGERIA; PROTEIN BINDING; PROTEIN INTERACTION MAPS; PROTEIN PRECURSORS; TWO-HYBRID SYSTEM TECHNIQUES;

EID: 84885390111     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2013.08.099     Document Type: Article

References (20)

1. Burtner C.R., Kennedy B.K. Progeria syndromes and ageing: what is the connection?. Nat. Rev. Mol. Cell Biol. 2010, 11:567-578.
2. Eriksson M., Brown W.T., Gordon L.B., et al. Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome. Nature 2003, 423:293-298.
3. Barrowman J., Hamblet C., Kane M.S., Michaelis S. Requirements for efficient proteolytic cleavage of prelamin A by ZMPSTE24. PLoS ONE 2012, 7:e32120.
4. Pendas A.M., Zhou Z., Cadinanos J., et al. Defective prelamin A processing and muscular and adipocyte alterations in Zmpste24 metalloproteinase-deficient mice. Nat. Genet. 2002, 31:94-99.
5. Liu B., Wang J., Chan K.M., et al. Genomic instability in laminopathy-based premature aging. Nat. Med. 2005, 11:780-785.
6. Varela I., Cadinanos J., Pendas A.M., et al. Accelerated ageing in mice deficient in Zmpste24 protease is linked to p53 signalling activation. Nature 2005, 437:564-568.
7. Scaffidi P., Misteli T. Lamin A-dependent nuclear defects in human aging. Science 2006, 312:1059-1063.
8. Ragnauth C.D., Warren D.T., Liu Y., et al. Prelamin A acts to accelerate smooth muscle cell senescence and is a novel biomarker of human vascular aging. Circulation 2010, 121:2200-2210.
9. Mattioli E., Columbaro M., Capanni C., et al. Prelamin A-mediated recruitment of SUN1 to the nuclear envelope directs nuclear positioning in human muscle. Cell Death Differ. 2011, 18:1305-1315.
10. Barton R.M., Worman H.J. Prenylated prelamin A interacts with Narf, a novel nuclear protein. J. Biol. Chem. 1999, 274:30008-30018.
11. Capanni C., Del Coco R., Mattioli E., et al. Emerin-prelamin A interplay in human fibroblasts. Biol. Cell 2009, 101:541-554.
12. Maraldi N.M., Capanni C., Lattanzi G., et al. SREBP1 interaction with prelamin A forms: a pathogenic mechanism for lipodystrophic laminopathies. Adv. Enzyme Regul. 2008, 48:209-223.
13. Ruiz de Eguino G., Infante A., Schlangen K., et al. Sp1 transcription factor interaction with accumulated prelamin a impairs adipose lineage differentiation in human mesenchymal stem cells: essential role of sp1 in the integrity of lipid vesicles. Stem Cells Transl. Med. 2012, 1:309-321.
14. Yang W., Itoh F., Ohya H., et al. Interference of E2-2-mediated effect in endothelial cells by FAM96B through its limited expression of E2-2. Cancer Sci. 2011, 102:1808-1814.
15. Ito S., Tan L.J., Andoh D., et al. MMXD, a TFIIH-independent XPD-MMS19 protein complex involved in chromosome segregation. Mol. Cell 2010, 39:632-640.
16. Gari K., Leon Ortiz A.M., Borel V., et al. MMS19 links cytoplasmic iron-sulfur cluster assembly to DNA metabolism. Science 2012, 337:243-245.
17. Stehling O., Vashisht A.A., Mascarenhas J., et al. MMS19 assembles iron-sulfur proteins required for DNA metabolism and genomic integrity. Science 2012, 337:195-199.
18. van Wietmarschen N., Moradian A., Morin G.B., et al. The mammalian proteins MMS19, MIP18, and ANT2 are involved in cytoplasmic iron-sulfur cluster protein assembly. J. Biol. Chem. 2012, 287:43351-43358.
19. Livesey K.M., Kang R., Zeh H.J., et al. Direct molecular interactions between HMGB1 and TP53 in colorectal cancer. Autophagy 2012, 8:846-848.
20. Liu B., Zhou Z. Lamin A/C, laminopathies and premature ageing. Histol. Histopathol. 2008, 23:747-763.