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| Faculty Research Interests | M.D. Anderson | GSBS

Randy L. Johnson, Ph.D.

RANDY L. JOHNSON, Ph.D.
Associate Professor

Department of Biochemistry and Molecular Biology
Room: S11.8136B
Telephone: 713-834-6287 / Fax: 713-834-6291
E-mail: rljohnso@mdanderson.org

Research interests

  • mouse genetics
  • pattern formation
  • development
  • gene targeting
 

Research in my laboratory focuses on genetic regulation of pattern formation, with emphasis on key regulators of limb, somite, and heart development. Our primary experimental systems are the mouse and manipulation of embryonic stem (ES) cells. At present we are in the process of developing new methodologies to facilitate rapid manipulation of the mouse germline through modification of ES cells. We plan to apply these methods to generate novel tools and reagents in order to analyze mutations in genes that play critical roles in development, differentiation, and disease.

Recent publications

  • Kokubo H, Miyagawa-Tomita S, Saga Y, Johnson RL (2005) Hesr1 and hesr2 are redundantly required for cardiac chamber formation and arterial specification. Dev Biol 278, 301–309.

  • Kile BT, Hentges KE, Clark AT, Nakamura H, Salinger AP, Box N, Liu B, Johnson RL, Behringer RR, Bradley A, Justice M (2003) Functional genetic analysis of mouse chromosome 11: large-scale isolation and rapid mapping of recessive mutations using a balancer chromosome. Nature 425, 81–86.

  • Kania A, Johnson RL, Jessell TM (2000) Coordinate roles for LIM homeobox genes in directing the dorsoventral trajectory of motor axons in the vertebrate limb. Cell 102, 161–173.

  • M. P. Smidt, C. Asbreuk, J. J. Cox, H. Chen, R. L. Johnson, J. P. H. Burbach (2000) A second independent pathway for development of mesencephalic dopaminergic neurons requires Lmx1b. Nature Neuroscience 3, 337–341.

  • C. L. Pressman, H. Chen, and R. L. Johnson (2000) Lmx1b, a LIM homeodomain class transcription factor, is necessary for normal development of multiple tissues in the anterior segment of the murine eye. Genesis 26, 15–25.

  • Lu MF, Pressman C, Dyer R, Johnson RL, Martin JF (1999) The function of the Rieger syndrome gene, Pitx2, in left-right morphogenesis and craniofacial development. Nature 401, 276–278.

  • Aulehla A, Johnson RL (1999) Dynamic expression of lunatic fringe suggests a link between notch signaling and an autonomous cellular oscillator driving somite segmentation. Dev Biol 207, 49–61

  • Evrard YA, Lun Y, Aulehla A, Gan L, Johnson RL (1998) lunatic fringe is an essential mediator of somite segmentation and patterning. Nature 394, 377–381.

  • Kengaku M, Capdevila J, Rodriguez-Esteban C, De La Peña J, Johnson RL, Izpisúa Belmonte J-C, Tabin CJ (1998) WNT3a regulates AER formation and utilizes an intracellular signaling pathway distinct from the dorsoventral signal WNT7a during chick limb morphogenesis. Science 280, 1274–1277.

  • Dreyer S, Zhou G, Winterpacht A, Zabel B, Cole W, Baldini A, Johnson RL, Lee B (1998) Mutations in LMX1B cause abnormal skeletal patterning and renal dysplasia in nail patella syndrome. Nature Genetics 19, 47–50.

  • Chen H, Lun Y, Ovchinnikov D, Kokubo H, Oberg KC, Pepicelli CV, Gan L, Lee B, Johnson RL (1998) Limb and kidney defects in lmx1b mutant mice suggest an involvement of LMX1B in human nail patella syndrome. Nature Genetics 19, 51–55.

  • Johnson RL, Tabin CJ (1997) Molecular models for vertebrate limb development. Cell 90, 979–990.

  • Levin M, Johnson RL, Stern CD, Kuehn M, Tabin C (1995) A molecular pathway determining left-right asymmetry in chick embryogenesis. Cell 82, 803–814.

  • Johnson RL, Laufer E, Riddle RD, Tabin CJ (1994) Ectopic expression of sonic hedgehog alters dorsal-ventral patterning of somites. Cell 79, 1165–1173.

  • Riddle RD, Johnson RL, Laufer E, Tabin C (1993) Sonic hedgehog mediates the polarizing activity of the ZPA. Cell 75, 1401–1416.

Mailing Address:
Department of Biochemistry and Molecular Biology, Unit 1000
U.T. M .D. Anderson Cancer Center
1515 Holcombe Boulevard
Houston, TX 77030

Last updated 11/22/2005