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Current Neurology and Neuroscience Reports

, Volume 12, Issue 3, pp 243–250 | Cite as

Recent Advances in the Genetics of the ALS-FTLD Complex

  • Huw R. MorrisEmail author
  • Adrian J. Waite
  • Nigel M. Williams
  • James W. Neal
  • Derek J. Blake
Genetics (V Bonifati, Section Editor)
First Online:

Abstract

There is a clinical and pathological overlap between amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD). A number of autosomal-dominant genes have been described that primarily cause ALS or FTLD such as progranulin (GRN), valosin-containing protein (VCP), and TAR DNA-Binding Protein (TARDBP), and for each of these conditions there are a small number of cases with both ALS and FTLD. Two major genes were described in 2011, which cause FTLD and/or ALS within extended kindreds. Ubiquilin2 (UBQLN2) is responsible for X-linked FTLD/ALS. A hexanucleotide repeat expansion in C9ORF72 causes chromosome 9p linked FTLD/ALS and is the most common cause of familial ALS accounting for about 40 % of familial cases. Both UBQLN2 and C9ORF72 mutations lead to TDP-43 positive neuropathology, and C9ORF72-positive cases have p62/ubiquitin-positive pathology, which is not stained by TDP-43 antibodies. Ubiquilin2 is one of a family of proteins thought to be important in targeting abnormal proteins for degradation via lysosomal and proteasomal routes. The pathogenic mechanism of the C9ORF72 expansion is unknown but may involve partial haploinsufficiency of C9ORF72 and/or the formations of toxic RNA inclusions. The identification of mutations in these genes represents an important step forward in our understanding of the clinical, pathological, and genetic spectrum of ALS/FTLD diseases.

Keywords

Frontotemporal dementia Frontotemporal lobar degeneration FTLD C9ORF72 Chromosome 9 Motor neuron disease Amyotrophic lateral sclerosis ALS Autosomal dominant X-linked Genetics UBQLN2 
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Notes

Disclosure

Conflicts of interest: H.R. Morris: has board membership with GlaxoSmithKline, Orion, Boehringer, Abbott, Solvay, and TEVA; has received grant support from Medical Research Council, Ipsen Fund, Welsh Assembly Government, Parkinson’s UK; has received payment for lectures including service on speakers bureaus from UCB Pharma, Orion, Boehringer, GlaxoSmithKline, TEVA; has received travel/accommodations/meeting expenses unrelated to activities listed from UCB, Orion, GlaxoSmithKline, Boehringer, TEVA; A.J. Waite: has received grant support from Motor Neuron Disease Association (MNDA), and has received support for travel to meetings for the study or other purposes from MNDA and Guarantors of brain; N.M. Williams: has received grant support from MNDA; J.W. Neal: none; D.J. Blake: has received grant support from MNDA.

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Copyright information

© Springer Science+Business Media, LLC 2012

Authors and Affiliations

  • Huw R. Morris
    • 1
    • 2
    • 4
    Email author
  • Adrian J. Waite
    • 1
  • Nigel M. Williams
    • 1
  • James W. Neal
    • 3
  • Derek J. Blake
    • 1
  1. 1.MRC Centre for Neuropsychiatric Genetics and GenomicsCardiff University School of MedicineCardiffUK
  2. 2.Department of NeurologyRoyal Gwent HospitalGwentUK
  3. 3.Department of PathologyCardiff University School of MedicineCardiffUK
  4. 4.Neurology (C4)University Hospital of WalesCardiffUK

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