Linkage analyses of event-related potential slow wave phenotypes recorded in a working memory task

Behavior Genetics

Volumn 36, Issue 1, 2006, Pages 29-44

  Hansell, N K ^a   Medland, S E ^a,b   Ferreira, M A R ^a   Geffen, G M ^b   Zhu, G ^a   Montgomery, G W ^a   Duffy, D L ^a   Wright, M J ^a   Martin, N G ^a  

^a QIMR BERGHOFER MEDICAL RESEARCH INSTITUTE   (Australia)

^b UNIVERSITY OF QUEENSLAND   (Australia)

Author keywords

Chromosome 10; MERLIN; Spatial working memory; Twins; Variance components

Indexed keywords

ADOLESCENT; ARTICLE; CHROMOSOME 10; CHROMOSOME 17; CHROMOSOME 20; CHROMOSOME 4; CHROMOSOME 5; CHROMOSOME 6; EMPIRICISM; EVENT RELATED POTENTIAL; GENE AMPLIFICATION; GENE CONTROL; GENE FUNCTION; GENETIC LINKAGE; GENOTYPE; HUMAN; LINKAGE ANALYSIS; MATHEMATICAL COMPUTING; PHENOTYPE; SPATIAL MEMORY; TASK PERFORMANCE; UNIVARIATE ANALYSIS; WAVEFORM; WORKING MEMORY;

ADOLESCENT; ANALYSIS OF VARIANCE; CHROMOSOME MAPPING; COMPUTER SIMULATION; EVOKED POTENTIALS; FEMALE; GENOTYPE; HUMANS; LOD SCORE; MALE; MEMORY; PHENOTYPE; TWINS, DIZYGOTIC; TWINS, MONOZYGOTIC;

EID: 33645768205     PISSN: 00018244     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10519-005-9002-2     Document Type: Article

References (57)

1. Abecasis, G. R., Burt, R. A., Hall, D., Bochum, S., Doheny, K. F., Lundy, S. L., Torrington, M., Roos, J. L., Gogos, J. A., and Karayiorgou, M. (2004). Genomewide scan in families with schizophrenia from the founder population of Afrikaners reveals evidence for linkage and uniparental disomy on chromosome 1. Am. J. Hum. Genet. 74:403-417.
2. Abecasis, G. R., Cherny, S. S., Cookson, W. O., and Cardon, L. R. (2002). Merlin-rapid analysis of dense genetic maps using sparse gene flow trees. Nat. Genet. 30:97-101.
3. Angata, K., Nakayama, J., Fredette, B., Chong, K., Ranscht, B., and Fukuda, M. (1997). Human STX polysialyltransferase forms the embryonic form of the neural cell adhesion molecule. J. Biol. Chem. 272:7182-7190.
4. Aubert, I., Ridet, J., Schachner, M., Rougon, G., and Gage, F. H. (1998). Expression of L1 and PSA during sprouting and regeneration in the adult hippocampal foundation. J. Comp. Neurol. 399:1-19.
5. Batuev, A. S., Shaffer, V. I., and Orlov, A. A. (1985). Comparative characteristics of unit activity in the prefrontal and parietal areas during delayed performance in monkeys. Behav. Brain Res. 16:57-70.
6. Bertram, L., Blacker, D., Mullin, K., Keeney, D., Jones, J., Basu, S., Yhu, S., McInnis, M. G., Go, R. C., Vekrellis, K., Selkoe, D. J., Saunders, A. J., and Tanzi, R. E. (2000). Evidence for genetic linkage of Alzheimer's disease to chromosome 10q. Science 290:2302-2303.
7. Chafee, M. V., and Goldman-Rakic, P. S. (2000). Inactivation of parietal and prefrontal cortex reveals interdependence of neural activity during memory-guided saccades. J. Neurophysiol. 83:1550-1566.
8. Coles, M. G. H. and M. D. Rugg (1995). Event-related brain potentials: an introduction. Electrophysiology of mind. M. D. Rugg and M. G. H. Coles. Oxford, Oxford University Press. 25:1-26
9. Cremer, H., Lange, R., Christoph, A., Plomann, M., Vopper, G., Roes, J., Brown, R., Baldwin, S., Kraemer, P., Scheff, S., et al. (1994). Inactivation of the N-CAM gene in mice results in size reduction of the olfactory bulb and deficits in spatial learning. Nature 367:455-459
10. Daly, G., Hawi, Z., Fitzgerald, M., and Gill, M. (1999). Mapping susceptibility loci in attention deficit hyperactivity disorder: preferential transmission of parental alleles at DAT1, DBH, and DRD5 to affected children. Mol. Psychiatry 4:192-196.
11. Davies, P., and Maloney, A. J. (1976). Selective loss of central cholinergic neurons in Alzheimer's disease. Lancet II:1403.
12. de Geus, E. J. C., Wright, M. J., Martin, N. G., and Boomsma, D. I. (2001). Genetics of brain function and cognition. Behav. Genet. 31:489-495.
13. de Koning, D. J., Visscher, P. M., Knott, S. A., and Haley, C. S. (1998). A strategy for QTL detection in half-sib populations. Anim. Sci. 67
14. Egan, M. F., Kojima, M., Callicott, J. H., Goldberg, T. E., Kolachana, B. S., Bertolina, A., Zaitsev, E., Gold, B., Goldman, D., Dean, M., Lu, B., and Weinberger, D. R. (2003). The BDNF val66met polymorphism affects activity-dependent secretion of BDNF and human memory and hippocampal function. Cell 112:257-269.
15. Engle, R. W., Cantor, J., and Carullo, J. J. (1992). Individual differences in working memory and comprehension: a test of four hypotheses. J. Exp. Psychol. Learn. Mem. Cogn. 18:972-992.
16. Faraone, S. V., Doyle, A. E., Mick, E., and Biederman, J. (2001). Meta-analysis of the association between the 7-repeat allele of the dopamine D(4) receptor gene and attention deficit hyperactivity disorder. Am. J. Psychiatry 158:1052-1057.
17. Flory, J. D., Manuck, S. B., Ferrell, R. E., Ryan, C. M., and Muldoon, M. F. (2000). Memory performance and the apolipoprotein E polymorphism in a community sample of middle-aged adults. Am. J. Med. Genet. 96:707-711.
18. Goldberg, T. E., Egan, M. F., Gscheidle, T., Coppola, R., Weickert, T., Kolachana, B. S., Goldman, D., and Weinberger, D. R. (2003). Executive subprocesses in working memory: relationship to catechol-O-methyltransferase Val158Met genotype and schizophrenia. Arch. Gen. Psychiatry 60:889-896.
19. Goldman-Rakic, P. S. (1996). Regional and cellular fractionation of working memory. Proc. Natl. Acad. Sci. USA 93:13473-13480.
20. Greenwood, P. M., and Parasuraman, R. (2003). Normal genetic variation, cognition, and aging. Behav. Cogn. Neurosci. Rev. 2:278-306.
21. Hansell, N., Wright, M., Geffen, G., Geffen, L., and Martin, N. (2002). Genetic covariation among ERP and performance measures of a working memory delayed-response task, information processing, and psychometric IQ. Psychophysiology 39:S3.
22. Hansell, N. K. (2003). A genetic investigation of brain function and cognitive ability. Brisbane: University of QueenslandUnpublished Doctoral Thesis.
23. Hansell, N. K., Wright, M. J., Geffen, G. M., Geffen, L. B., and Martin, N. G. (2004). Genetic influence on cognitive processes of distraction: an event-related potential study of the slow wave. Aust. J. Psychol. 56:89-98.
24. Hansell, N. K., Wright, M. J., Geffen, G. M., Geffen, L. B., Smith, G. A., and Martin, N. G. (2001). Genetic influence on ERP slow wave measures of working memory. Behav. Genet. 31:603-614.
25. Harold, D., Peirce, T., Moskvina, V., Myers, A., Jones, S., Hollingworth, P., Moore, P., Lovestone, S., Powell, J., Foy, C., Archer, N., Walter, S., Edmonson, A., McIlroy, S., Craig, D., Passmore, P. A., Goate, A., Hardy, J., O'Donovan, M., Williams, J., Liddell, M., Owen, M. J., and Jones, J. (2003). Sequence variation in the CHAT locus shows no association with late-onset alzheimer's disease. Hum. Genet. 113:258-267.
26. Jones, K. A., Projesz, B., Almasy, L., Bierut, L., Goate, A., Wang, J. C., Dick, D. M., Hinrichs, A., Kwon, J., Rice, J. P., Rohrbaugh, J., Stock, H., Wu, W., Bauer, L. O., Chorlian, D. B., Crowe, R. R., Edenberg, H. J., Foroud, T., Hesselbrock, V., Kuperman, S., Nurnberger, J., O'Connor, S. J., Schuckit, M. A., Stimus, A. T., Tischfield, J. A., Reich, T., and Begleiter, H. (2004). Linkage and linkage disequilibrium of evoked EEG oscillations with CHRM2 receptor gene polymorphisms: implications for human brain dynamics and cognition. Int. J. Psychophysiol. 53:75-90.
27. Jonides, J., Smith, E. E., Koeppe, R. A., Awh, E., Minoshima, S., and Mintum, M. A. (1993). Spatial working memory in humans as revealed by PET. Nature 363:623-625.
28. Kadmon, G., Kowitz, A., Altevogt, P., and Schachner, M. (1990). Functional cooperation between the neural adhesion molecules L1 and N-CAM is carbohydrate dependent. J. Cell Biol. 110:209-218.
29. Kapfhamer, D., Miller, D. E., Lambert, S., Bennett, V., Glover, T. W., and Burmeister, M. (1995). Chromosomal localization of the ankyrin-G gene (ANK3/Ank3) to human 10q21 and mouse 10. Genomics 27:189-191.
30. Kong, A., Gudbjartsson, D. F., Sainz, J., Jonsdottir, G. M., Gudjonsson, S. A., Richardsson, B., Sigurdardottir, S., Barnard, J., Hallbeck, B., Masson, G., Shlien, A., Palsson, S. T., Frigge, M. L., Thorgeirsson, T. E., Gulcher, J. R., and Stefansson, K. (2002). A high-resolution recombination map of the human genome. Nat. Genet. 31:241-247.
31. G: a new ankyrin gene with neural-specific isoforms localized at the axonal initial segment and node of ranvier. J. Biol. Chem. 270:2352-2359.
32. Kyllonen, P. C., and Christal, R. E. (1990). Reasoning ability is (little more than) working-memory capacity. Intelligence 14:389-433.
33. Lander, E., and Kruglyak, L. (1995). Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results. Nat. Genet. 11:241-247.
34. Leal, S. M. (2003). Genetic maps of microsatellite and single-nucleotide polymorphism markers: are the distances accurate? Genet. Epidemiol. 24:243-252.
35. Levi-Montalcini, R. (1998). The saga of the nerve growth factor. Neuroreports 9:R71-83.
36. Lezcano, N., Mrzljak, L., Eubanks, S., Levenson, R., Goldman-Rakic, P., and Bergson, C. (2000). Dual signaling regulated by calcyon, a D1 dopamine receptor interacting protein. Science 287:1660-1664.
37. Marin, O., Yaron, A., Bagri, A., Tessier-Lavigne, M., and Rubenstein, J. L. R. (2001). Sorting of striatal and cortical interneurons regulated by semaphorin-neuropilin interactions. Science 293:872-875.
38. Morley, K., and Montgomery, G. W. (2001). The genetics of cognitive processes: candidate genes in humans and animals. Behav. Genet. 31:511-531.
39. Muller, U., von Cramon, D. Y., and Pollmann, S. (1998). D1 versus D2-receptor modulation of visuospatial working memory in humans. J. Neurosci. 18:2720-2728.
40. Myers, A., Holmans, P., Marshall, H., Kwon, J., Meyer, D., Ramic, D., Shears, S., Booth, J., DeVrieze, F. W., Crook, R., Hamshere, M., Abraham, R., Tunstall, N., Rice, F., Carty, S., Lillystone, S., Kehoe, P., Rudrasingham, V., Jones, L., Lovestone, S., Perez-Tur, J., Williams, J., Owen, M. J., Hardy, J., and Goate, A. M. (2000). Susceptibility locus for Alzheimer's disease on chromosome 10. Science 290:2304-2305.
41. Nakayama, J., Fukuda, M. N., Fredette, B., Rauscht, B., and Fukuda, M. (1995). Expression cloning of a human polysialyltransferase that forms the polysialylated neural cell adhesion molecule present in embryonic brain. Proc. Natl. Acad. Sci. USA 92:7031-7035.
42. Ohno, K., Tsujina, A., Brengman, J. M., Harper, C. M., Bajzer, Z., Udd, B., Beyring, R., Robb, S., Kirkham, F. J., and Engel, A. G. (2001). Choline acetyltransferase mutations cause myasthenic syndrome associated with episodic apnea in humans. Proc. Nat. Acad. Sci. 98:2017-2022.
43. Plomin, R., McClearn, G. E., Smith, D. L., Skuder, P., Vignetti, S., Chorney, M. J., Chorney, K., Kasarda, S., Thompson, L. A., Detterman, D. K., Petrill, S. A., Daniels, J., Owen, M. J., and McGuffin, P. (1995). Allelic associations between 100 DNA markers and high versus low IQ. Intelligence 21:31-48.
44. Rossignol, M., Beggs, A. H., Pierce, E. A., and Klagsbrun, M. (1999). Human neuropilin-1 and neuropilin-2 map to 10p12 and 2q34, respectively. Genomics 57:459-460.
45. Rowe, J. B., Toni, I., Josephs, O., Frackowiak, R. S. J., and Passingham, R. E. (2000). The prefrontal cortex: response selection or maintenance within working memory. Science 288:1656-1660.
46. Rutishauser, U., Acheson, A., Hall, A. K., Mann, D. M., and Sunshine, J. (1988). The neural cell adhesion molecule (NCAM) as a regulator of cell-cell interactions. Science 240:53-57.
47. Sawaguchi, T. (1997). Attenuation of preparatory activity for reaching movements by a D1-dopamine antagonist in the monkey premotor cortex. J. Neurophysiol. 78:1769-1774.
48. Smith, E. E., and Jonides, J. (1998). Neuroimaging analyses of human working memory. Proc. Natl. Acad. Sci. USA 95:12061-12068.
49. Spelman, R. J., Coppieters, W., Karim, L., van Arendonk, J. A., and Bovenhuis, H. (1996). Quantitative trait loci analysis for five milk production traits on chromosome six in the Dutch Holstein-Friesian population. Genetics 67:257-268.
50. Steinlein, O. K., Magnusson, A., Stoodt, J., Bertrand, S., Weiland, S., Berkovic, S. F., Nakken, K. O., Propping, P., and Bertrand, D. (1997). An insertion mutation of the CHRNA4 gene in a family with autosomal dominant nocturnal frontal lobe epilepsy. Hum. Mol. Genet. 6:943-947.
51. Tang, J., Rutishauser, U., and Landmesser, L. (1994). Polysialic acid regulates growth cone behavior during sorting of motor axons in the plexus region. Neuron 13:405-414.
52. Tomasiewicz, H., Ono, K., Yee, D., Thompson, C., Goridis, C., Rutishauser, U., and Magnuson, T. (1993). Genetic deletion of a neural cell adhesion molecule variant (N-CAM-180) produces distinct defects in the central nervous system. Neuron 11:1163-1174.
53. Viegas-Pequignot, E., Berrard, S., Brice, A., Apiou, F., and Mallet, J. (1991). Localization of a 900-bp-long fragment of the human choline acetyltransferase gene to 10q 11.2 by nonradioactive in situ hybridization. Genomics 9:210-212.
54. Wilson, K. M., and Swanson, H. L. (2001). Are mathematics disabilities due to a domain-general or a domain-specific working memory deficit. J. Learn. Disabil. 34:237-248.
55. Wright, M., De Geus, E., Ando, J., Luciano, M., Posthuma, D., Ono, Y., Hansell, N., Van Baal, C., Hiraishi, K., Hasegawa, T., Smith, G., Geffen, G., Geffen, L., and Kanba, S. (2001). Genetics of cognition: outline of a collaborative twin study. Twin Res. 4:48-56.
56. Zhu, G., Duffy, D. L., Eldridge, A., Grace, M., Mayne, C., O'Gorman, L., Aitken, J. F., Neale, M. C., Hayward, N. K., Green, A. C., and Martin, N. G. (1999). A major quantitative-trait locus for mole density is linked to the familial melanoma gene CDKN2A: a maximum-likelihood combined linkage and association analysis in twins and their sibs. Am. J. Hum. Genet. 65:483-492.
57. Zhu, G., Evans, D. M., Duffy, D. L., Montgomery, G. W., Medland, S. E., Gillespie, N. A., Ewen, K. R., Jewell, M., Liew, Y. W., Hayward, N. K., Sturm, R. A., Trent, J. M., and Martin, N. G. (2004). A genome scan for eye color in 502 twin families: most variation is due to a QTL on Chromosome 15q. Twin Res. 7:197-210.