Neurofibromin 1

Neurofibromin 1

PDB rendering based on 1nf1.
Identifiers
Symbols NF1; DKFZp686J1293; FLJ21220; NFNS; VRNF; WSS
External IDs OMIM613113 MGI97306 HomoloGene226 GeneCards: NF1 Gene
Orthologs
Species Human Mouse
Entrez 4763 18015
Ensembl ENSG00000196712 ENSMUSG00000020716
UniProt P21359 Q3TYD2
RefSeq (mRNA) NM_000267.3 NM_010897.2
RefSeq (protein) NP_000258.1 NP_035027.1
Location (UCSC) Chr 17:
29.42 – 29.71 Mb
Chr 11:
79.15 – 79.4 Mb
PubMed search [1] [2]

Neurofibromin 1 also known as neurofibromatosis-related protein NF-1 is a protein that in humans is encoded by the NF1 gene.[1] Mutations in the NF1 gene are associated with neurofibromatosis type I (also known as neurofibromatosis, von Recklinghausen disease, and Watson disease).[2]

Contents

Function

NF1 encodes the protein neurofibromin, which appears to be a negative regulator of the ras signal transduction pathway.

NF1 is found within the mammalian postsynapse, where it is known to bind to the NMDA receptor complex. It has been found to lead to deficits in learning, and it is suspected that this is a result of its regulation of the Ras pathway. It is known to regulate the GTPase HRAS, causing the hydrolyzation of GTP and thereby inactivating it.[3] Within the synapse HRAS is known to activate Src, which itself phosphorylates GRIN2A, leading to its inclusion in the synaptic membrane.

NF1 is also known to interact with CASK through syndecan, a protein which is involved in the KIF17/ABPA1/CASK/LIN7A complex, which is involved in trafficking GRIN2B to the synapse. This suggests that NF1 has a role in the transportation of the NMDA receptor subunits to the synapse and its membrane. NF1 is also believed to be involved in the synaptic ATP-PKA-cAMP pathway, through modulation of adenylyl cyclase. It is also known to bind the caveolin 1, a protein which regualtes p21ras, PKC and growth response factors.[3]

Clinical significance

Mutations linked to neurofibromatosis type 1 led to the identification of the NF1 gene. In addition to neurofibromatosis type I, mutations in NF1 can also lead to juvenile myelomonocytic leukemia and Watson syndrome.[4]

Types of Mutations

The neurofibromin gene may be mutated in thousands of ways, resulting in many possible clinical outcomes.[5] Types of mutations include frameshift, nonsense, missense, splicing alteration and deletion mutations, and loss of heterozygosity.[6][7][8][9]

RNA editing

Type

The type of editing is a cytidine to uridine (C to U) site specific deamination. The editing site in NF1 mRNA was determined to have a high homology to the ApoB editing site where double stranded mRNA undergoes editing by the ApoB holoenzyme.[10] This alluded to the same holoenzyme involved in ApoB mRNA editing maybe involved in editing of NF1.[11] There are at least four different alternatively spliced forms of the protein, two of which are better defined. They differ by the inclusion of exon 23A. Recent experiments have shown that apobec-1 is indeed expressed outside the GI luminal tract in some tumors and the inclusion of downstream exon 23a is preferentially found in these edited transcripts. These two features distinguishes them from tumors where RNA editing does not occur.[12]

Location

The cytidine in the arginine codon (CGA) is deaminated to a uracil creating an inframe translational stop codon. The editing site is located at nucleotide position 2914.A region (nucleotides 2909-2930) was found to have a high homology to that found in the 21 nucleotide editing region of ApoB mRNA. It was suggested that the same editsome involved in ApoB mRNA editing may also be involved in NF1 mRNA editing. However the 6 nucleotide stretch from the edited cytidine and the start of the mooring sequence is two nucleotides longer than the ideal sequence required for ApoB mRNA editing. Also the region contains 2 guanidines which would be tolerated but again would not be ideal for ApoB mRNA editing. The mooring sequence and regulatory sequence are thought to be sufficent for editing to occur by ApoB mRNA editing machinery. This was determined by site mutagenesis experiments.[13]

Regulation

NF1 RNA editing is not regulated by limited amounts of APOBEC-1. This implies that different factors are involved in NF1 mRNA editing than those associated with ApoB RNA editing. It is thought that different trans acting factors may be involved in the two editing processes.[10] Also, the region surrounding the editing region in NF1 mRNA is GC rich instead of the preferred AT rich sequence found in ApoB mRNA editing site. This reason as well as the longer spacer element of NF1 mRNA than that of ApoB mRNA are thought to be factors in the difference in frequency of editing of the two mRNAs (20% NF1, 90% ApoB).[14] Editing occurs in a higher frequency in tumours compared to the relative normal tissues.[10] There is a higher frequency of edting in the NF1 mRNA which includes Exon 23A in tumors.[12]

Conservation

The editing site is thought not to be conserved as editing of NF1 mRNA does not occur in the rat or mouse but these species do express several alternatively spliced mRNAs.[10][15] One of these alternatively spliced isoforms known as TYPE III in rats and mice introduces a frameshift that introduces a stop codon by inclusion of a 41 base pair exon.[16]

Consequences

Structure

Editing results in a codon change from an arginine codon (CGA) to an in frame stop codon (UGA) due to a base change at nucleotide 2914. The introduction of an inframe stop codon results in a translated protein that is truncated. The translated protein is thought to be lacking its GAP Related Domain (GRD) that shares a homology to mammalian GTPase activating (GAP) domain and yeast inhibitor of RAS protein 1 and 2 domains.[10]

Function

The gene product is neurofibromin, a tumor-suppressor , a region of which functions as a GTPase-activating protein shown to be involved in negative regulation of the RAS pathway.[17][16] NF1 mRNA editing has been detected in a wide range of tissues. Editing results in a truncated protein being translated that does not contain this region. The GTPase region has a high homology to with mammalian and yeast (GAPs) which would suggest that neurofibromin plays a role in negative regulation of RAS signal transduction pathways. It is thought that editing therefore would result in the loss of the proteins tumour supressor activity.[18][19][20] This corresponds to the observed increase in editing in tumors compared to normal tissue , however further research into the role of mRNA editing of NF1 mRNA in pathogenesis in tumours needs to be undertaked.[10][15] There is a correlation in an increase of editing in some tumors and the degree of malignancy of the tumor suggesting a relationship between the two.[16] Recently further evidence of the role of editing in pathogenesis in tumors.It was observed that C to U editing of NF1 mRNA occurs in a fraction of tumor samples of NF1 patients where APOBEC-1 is also expressed. This was an important find as was the first time APOBEC-1 expression was proven experimentally outside the luminal cells of the tract.[12] The N-terminus of the protein has a region demonstrated to be able to bind microtubules. It has been suggested that since the edited protein still retains this region, that a function of this editing is to displace microtubules from the full length neurofiromin protein. This would liberate the full length protein to interact with RAS.[15][21]

Neurofibromitosis

It is thought that RNA editing may account for the wide variation in phenotype of this condition even among siblings.[22] Also 50% of new cases have new mutations. The frequency is too high to explain these cases as spontaneous mutations therefore RNA editing of NF1 rna may provide an alternative reason for the variation of phenotype.[11]

Patent

The neurofibromatosis gene was patented by the University of Michigan, with the intitial filing in 1991 and the patent granted in 2001.[23]

See also

  • SPRED1 gene

References

  1. ^ Skuse GR, Kosciolek BA, Rowley PT (September 1991). "The neurofibroma in von Recklinghausen neurofibromatosis has a unicellular origin". Am. J. Hum. Genet. 49 (3): 600–7. PMC 1683134. PMID 1715669. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1683134. 
  2. ^ Rasmussen SA, Friedman JM (January 2000). "NF1 gene and neurofibromatosis 1". Am. J. Epidemiol. 151 (1): 33–40. PMID 10625171. 
  3. ^ a b Trovó-Marqui AB, Tajara EH (2006). "Neurofibromin: a general outlook.". Clin. Genet. 70 (1): 1–13. doi:10.1111/j.1399-0004.2006.00639.x. PMID 16813595. 
  4. ^ "Entrez Gene: NF1 neurofibromin 1 (neurofibromatosis, von Recklinghausen disease, Watson disease)". http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=4763. 
  5. ^ "NF1 mutations and molecular testing", by SA Thomson, L Fishbein and MR Wallace, J Child Neurol 2002 Aug; 17(8); 555-61; discussion 571-2, 646-51
  6. ^ "Germline and somatic NF1 mutations in sporadic and NF1-associated malignant peripheral nerve sheath tumours", by Bottillo I, Ahlquist T, Brekke H, Danielsen SA, van den Berg E, Mertens F, Lothe RA, Dallapiccola B. J Pathol. 2009 Apr;217(5):693-701. PMID: 19142971
  7. ^ "Nf1 tumor suppressor in skin:: Expression in response to tissue trauma and in cellular differentiation"
  8. ^ "Toward a Survey of Somatic Mutation of the NF1 Gene in Benign Neurofibromas of Patients with Neurofibromatosis Type 1", by Ingrid Eisenbarth, Kim Beyer,* Winfrid Krone, and Günter Assum, Am J Hum Genet. 2000 February; 66(2): 393–401. PMCID: PMC1288091
  9. ^ "Neurofibromatosis: Novel and Recurrent Mutations in Turkish Patients", by Yunus Kasim Terzi, Sibel Oguzkan, Banu Anlar, Sabiha Aysun, Sukriye Ayter. Pediatric neurology 1 December 2007 (volume 37 issue 6 Pages 421-425 DOI: 10.1016/j.pediatrneurol.2007.07.005)
  10. ^ a b c d e f Skuse GR, Cappione AJ, Sowden M, Metheny LJ, Smith HC (February 1996). "The neurofibromatosis type I messenger RNA undergoes base-modification RNA editing". Nucleic Acids Res. 24 (3): 478–85. doi:10.1093/nar/24.3.478. PMC 145654. PMID 8602361. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=145654. 
  11. ^ a b Skuse GR, Ludlow JW (April 1995). "Tumour suppressor genes in disease and therapy". Lancet 345 (8954): 902–6. doi:10.1016/S0140-6736(95)90015-2. PMID 7707816. 
  12. ^ a b c Mukhopadhyay D, Anant S, Lee RM, Kennedy S, Viskochil D, Davidson NO (January 2002). "C-->U editing of neurofibromatosis 1 mRNA occurs in tumors that express both the type II transcript and apobec-1, the catalytic subunit of the apolipoprotein B mRNA-editing enzyme". Am. J. Hum. Genet. 70 (1): 38–50. doi:10.1086/337952. PMC 384902. PMID 11727199. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=384902. 
  13. ^ Backus JW, Smith HC (November 1992). "Three distinct RNA sequence elements are required for efficient apolipoprotein B (apoB) RNA editing in vitro". Nucleic Acids Res. 20 (22): 6007–14. doi:10.1093/nar/20.22.6007. PMC 334467. PMID 1461733. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=334467. 
  14. ^ Driscoll DM, Zhang Q (August 1994). "Expression and characterization of p27, the catalytic subunit of the apolipoprotein B mRNA editing enzyme". J. Biol. Chem. 269 (31): 19843–7. PMID 8051066. 
  15. ^ a b c Skuse GR, Cappione AJ (1997). "RNA processing and clinical variability in neurofibromatosis type I (NF1)". Hum. Mol. Genet. 6 (10): 1707–12. doi:10.1093/hmg/6.10.1707. PMID 9300663. 
  16. ^ a b c Cappione AJ, French BL, Skuse GR (February 1997). "A potential role for NF1 mRNA editing in the pathogenesis of NF1 tumors". Am. J. Hum. Genet. 60 (2): 305–12. PMC 1712412. PMID 9012403. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1712412. 
  17. ^ Cichowski K, Jacks T (February 2001). "NF1 tumor suppressor gene function: narrowing the GAP". Cell 104 (4): 593–604. doi:10.1016/S0092-8674(01)00245-8. PMID 11239415. 
  18. ^ Brannan CI, Perkins AS, Vogel KS, Ratner N, Nordlund ML, Reid SW, Buchberg AM, Jenkins NA, Parada LF, Copeland NG (May 1994). "Targeted disruption of the neurofibromatosis type-1 gene leads to developmental abnormalities in heart and various neural crest-derived tissues". Genes Dev. 8 (9): 1019–29. doi:10.1101/gad.8.9.1019. PMID 7926784. 
  19. ^ Ballester R, Marchuk D, Boguski M, Saulino A, Letcher R, Wigler M, Collins F (November 1990). "The NF1 locus encodes a protein functionally related to mammalian GAP and yeast IRA proteins". Cell 63 (4): 851–9. doi:10.1016/0092-8674(90)90151-4. PMID 2121371. 
  20. ^ Xu GF, O'Connell P, Viskochil D, Cawthon R, Robertson M, Culver M, Dunn D, Stevens J, Gesteland R, White R (August 1990). "The neurofibromatosis type 1 gene encodes a protein related to GAP". Cell 62 (3): 599–608. doi:10.1016/0092-8674(90)90024-9. PMID 2116237. 
  21. ^ Gregory PE, Gutmann DH, Mitchell A, Park S, Boguski M, Jacks T, Wood DL, Jove R, Collins FS (May 1993). "Neurofibromatosis type 1 gene product (neurofibromin) associates with microtubules". Somat. Cell Mol. Genet. 19 (3): 265–74. doi:10.1007/BF01233074. PMID 8332934. 
  22. ^ Huson SM, Compston DA, Clark P, Harper PS (November 1989). "A genetic study of von Recklinghausen neurofibromatosis in south east Wales. I. Prevalence, fitness, mutation rate, and effect of parental transmission on severity". J. Med. Genet. 26 (11): 704–11. doi:10.1136/jmg.26.11.704. PMC 1015740. PMID 2511318. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1015740. 
  23. ^ United States Patent US006238861B1

Further reading

External links


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