The lissencephaly gene product Lis1, a protein involved in neuronal migration, interacts with a nuclear movement protein, NudC

Current Biology

Volumn 8, Issue 10, 1998, Pages 603-606

  Morris, S M ^a   Albrecht, U ^a   Reiner, O ^b   Eichele, G ^a,c   Yu Lee, L Y ^a  

^a BAYLOR COLLEGE OF MEDICINE   (United States)

^b WEIZMANN INSTITUTE OF SCIENCE   (Israel)

^c ALBERT EINSTEIN INSTITUT   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

1 ALKYL 2 ACETYLGLYCEROPHOSPHOCHOLINE ESTERASE; ASPERGILLUS NIDULANS; GENE MUTATION; MICROTUBULE; MILLER DIEKER SYNDROME; PROTEIN INTERACTION; TUBULIN;

ACRONICTA LEPORINA; ASPERGILLUS; EMERICELLA NIDULANS; MAMMALIA; MURINAE;

EID: 0032493049     PISSN: 09609822     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-9822(98)70232-5     Document Type: Article

References (35)

1. Sheldon M, Rice DS, D'Arcangelo G, Yoneshima H, Nakajima K, Mikoshiba K, et al.: Scrambler and yotari disrupt the disabled gene and produce a reeler-like phenotype in mice. Nature 1997, 389:730-733.
2. Howell BW, Hawkes R, Soriano P, Cooper JA: Neuronal position in the developing brain is regulated by mouse disabled-1. Nature 1997, 389:733-737.
3. Reiner O, Carrozzo R, Shen Y, Wehnert M, Faustinella F, Dobyns WB, et al.: Isolation of a Miller-Dieker lissencephaly gene containing G protein β-subunit-like repeats. Nature 1993, 364:717-721.
4. des Portes V, Pinard JM, Billuart P, Vinet MC, Koulakoff A, Carrie A,et al.: A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome. Cell 1998, 92:51-61.
5. Gleeson JG, Allen KM, Fox JW, Lamperti ED , Berkovic S, Scheffer I, et al.: doublecortin, a brain-specific gene mutated in human X-linked Lissencephaly and Double Cortex Syndrome, encodes a putative signaling protein. Cell 1998, 92:63-72.
6. Lo Nigro C, Chong SS, Smith ACM, Dobyns WB, Carrozzo R, Ledbetter DH: Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndrome. Hum Mol Genet 1997, 6:157-164.
7. Dobyns WB, Truwit CL: Lissencephaly and other malformations of cortical development: 1995 update. Neuropediatrics 1995, 26:132-147.
8. Barkovich AJ, Kuzniecky RI, Dobyns WB, Jackson GD, Becker LE, Evrard P: A classification scheme for malformations of cortical development. Neuropediatrics 1996, 27:59-63.
9. Reiner O, Albrecht U, Gordon M, Chianese KA, Wong C, Gal-Gerber O, et al.: Lissencephaly gene (LIS1) expression in the CNS suggests a role in neuronal migration. J Neurosci 1995, 15:3730-3738.
10. Albrecht U, Abu-Issa R, Ratz B, Hattori M, Aoki J, Arai H,et al.: Platelet-activating factor acetylhydrolase expression and activity suggest a link between neuronal migration and platelet-activating factor. Dev Biol 1996, 180:579-593.
11. Neer EJ, Schmidt CJ, Nambudripad R, Smith TF: The ancient regulatory-protein family of WD-repeat proteins. Nature 1994, 371:297-300.
12. Hattori M, Adachi H, Tsujimoto M, Arai H, Inoue K: Miller-Dieker lissencephaly gene encodes a subunit of brain platelet-activating factor. Nature 1994, 370:216-218.
13. Sapir T, Elbaum M, Reiner O: Reduction of microtubule catastrophe events by LIS1, platelet-activating factor acetylhydrolase subunit. EMBO J 1997, 16:6977-6984.
14. Osmani AH, Osmani SA, Morris NR: The molecular cloning and identification of a gene product specifically required for nuclear movement in Aspergillus nidulans. J Cell Biol 1990, 111:543-551.
15. Fields S, Song O: A novel genetic system to detect protein-protein interactions. Nature 1989, 340:245-246.
16. Morris SM, Anaya P, Xiang X, Morris NR, May GS, Yu-Lee L-y: A prolactin-inducible T cell gene product is structurally similar to the Aspergillus nidulans nuclear movement protein NUDC. Mol Endocrinol 1997, 11:229-236.
17. Cunniff J, Chiu Y-H, Morris NR, Warrior R: Characterization of Dnud C, the Drosophila homolog of an Aspergillus gene that functions in nuclear motility. Mech Dev 1997, 66:55-68.
18. Xiang X, Osmani AH, Osmani SA, Xin M, Morris NR: NudF, a nuclear migration gene in Aspergillus nidulans, is similar to the human LIS-1 gene required for neuronal migration. Mol Biol Cell 1995, 6:297-310.
19. Axtell SM, Truong TM, O'Neal KD, Yu-Lee L-y: Characterization of a prolactin-inducible gene, clone 15, in T cells. Mol Endocrinol 1995, 9:312-318.
20. McConnell SK: Constructing the cerebral cortex: Neurogenesis and fate determination. Neuron 1995, 15:761-768.
21. Barth PG: Disorders of neuronal migration. Can J Neurol Sci 1987, 14:1-16.
22. Sauer FC: Mitosis in the neural tube. J Comp Neurol 1935, 62:377-405.
23. McConnell SK, Kaznowski CE: Cell cycle dependence of laminar determination in developing cerebral cortex. Science 1991, 254:282-285.
24. Oakley BR, Morris NR: Nuclear movement is β-tubulin-dependent in Aspergillus nidulans. Cell 1980, 19:255-262.
25. Xiang X, Beckwith SM, Morris NR: Cytoplasmic dynein is involved in nuclear migration in Aspergillus nidulans. Proc Natl Acad Sci USA 1994, 91:2100-2104.
26. Willins DA, Liu B, Xiang X, Morris NR: Mutations in the heavy chain of cytoplasmic dynein suppress the nudF nuclear migration mutation of Aspergillus nidulans. Mol Gen Genet 1997, 255:194-200.
27. Chiu Y-H, Morris NR: Extragenic suppressors of nudC3, a mutation that blocks nuclear migration in Aspergillus nidulans. Genetics 1995, 141:453-464.
28. Mizuguchi M, Takashima S, Kakita A, Yamada M, Ikeda K: Lissencephaly gene product: Localization in the central nervous system and loss of immunoreactivity in Miller-Dieker syndrome. Am J Physiol 1995, 147:1142-1151.
29. Hager G, Dodt H-U, Zieglgansberger W, Liesi P: Novel forms of neuronal migration in the rat cerebellum. J Neurosci Res 1995, 40:207-219.
30. O'Neal KD, Schwarz LA, Yu-Lee L-y: Prolactin receptor gene expression in lymphoid cells. Mol Cell Endocrinol 1991, 82:127-135.
31. James P, Halladay J, Craig EA: Genomic libraries and a host strain designed for highly efficient two-hybrid selection in yeast. Genetics 1996, 144:1425-1436.
32. Morris SM, Yu-Lee L-y: Expression of RNUDC, a potential nuclear movement protein, in mammalian cells: Localization to the Golgi apparatus. Exp Cell Res 1998, 238:23-32.
33. Garcia-Higuera I, Genoglio J, Li Y, Lewis C, Panchenko M, Reiner O, et al.: Folding of proteins with WD-repeats: Comparison of six members of the WD-repeat superfamily to the G protein β subunit. Biochemistry 1996, 35:13985-13994.
34. Luo G, Yu-Lee L-y: Transcriptional inhibition by Stat5: Differential activities at growth-related versus differentiation-specific promoters. J Biol Chem 1997, 272:26841-26849.
35. Albrecht U, Lu H-C, Revelli J-P, Xu X-C, Lotan R, Eichele G: Studying gene expression on tissue sections using in situ hybridization. In Human Genome Methods. Edited by Adolph KW. Boca Raton: CRC Press; 1998:93-120.