A defect in nurturing in mice lacking the immediate early gene fosB

Cell

Volumn 86, Issue 2, 1996, Pages 297-309

  Brown, Jennifer R ^a,b   Ye, Hong ^a,b   Bronson, Roderick T ^c   Dikkes, Pieter ^a   Greenberg, Michael E ^a,b  

^a BOSTON CHILDREN S HOSPITAL   (United States)

^b HARVARD MEDICAL SCHOOL   (United States)

^c NONE

Author keywords

[No Author keywords available]

Indexed keywords

ONCOPROTEIN;

ADAPTATION; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; CONTROLLED STUDY; FEMALE; GENE EXPRESSION; GENE TARGETING; HISTOPATHOLOGY; IMMEDIATE EARLY GENE; MAMMARY GLAND FUNCTION; MATERNAL BEHAVIOR; MOUSE; NONHUMAN; ONCOGENE C FOS; PREOPTIC AREA; PRIORITY JOURNAL; TRANSCRIPTION REGULATION;

EID: 0030602817     PISSN: 00928674     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0092-8674(00)80101-4     Document Type: Article

References (61)

1. Abeliovich, A., Paylor, R., Chen, C., Kim, J.J., Wehner, J.M., and Tonegawa, S. (1993). PKCγ mutant mice exhibit mild deficits in spatial and contextual learning. Cell 75, 1263-1271.
2. Ausubel, F.M., Brent, R., Kingston, R.E., Moore, D.D., Seidman, J.G., Smith, J.A., and Struhl, K. (1995). Current Protocols in Molecular Biology, K. Janssen, ed. (Boston: John Wiley and Sons, Inc.).
3. Bading, H., Ginty, D.D., and Greenberg, M.E. (1993). Regulation of gene expression in hippocampal neurons by distinct calcium signalling pathways. Science 260, 181-186.
4. Barnett, S.A., and Burn, J. (1970). Maternal and infant behavior. In Reproduction and Breeding Techniques for Laboratory Animals, E.S.E. Hafez, ed. (Philadelphia: Lea and Febiger).
5. Bridges, R.S. (1994). The role of lactogenic hormones in maternal behavior in female rats. Acta Ped. (Suppl.) 397, 33-39.
6. Bridges, R.S., and Mann, P.E. (1994). Prolactin-brain interactions in the induction of maternal behavior in rats. Psychoneuroendoc. 19, 611-622.
7. Calamandrei, G., and Keverne, E.B. (1994). Differential expression of Fos protein in the brain of female mice dependent on pup sensory cues and maternal experience. Behav. Neurosci. 108, 113-120.
8. Church, G.M., and Gilbert, W. (1984). Genomic sequencing. Proc. Natl. Acad. Sci. USA 81, 1991-1995.
9. Demmer, J., Dragunow, M., Lawlor, P.A., Mason, S.E., Leah, J.D., Abraham, W.C., and Tate, W.P. (1993). Differential expression of immediate early genes after hippocampal long-term potentiation in awake rats. Mol. Brain Res. 17, 279-286.
10. Fahrbach, S.E., Morrell, J.I., and Pfaff, D.W. (1985). Possible role for endogenous oxytocin in estrogen-facilitated maternal behavior in rats. Neuroendocr. 40, 526-532.
11. Fleming, A.S., and Rosenblatt, J.S. (1974). Olfactory regulation of maternal behavior in rats: I. Effects of olfactory bulb removal in experienced and inexperienced lactating and cycling females. J. Comp. Physiol. Psych. 86, 221-232.
12. Fleming, A.S., and Walsh, C. (1994). Neuropsychology of maternal behavior in the rat: c-fos expression during mother-litter interactions. Psychoneuroendoc. 19, 429-443.
13. Fleming, A.S., Vaccarino, F., and Luebke, C. (1980). Amygdaloid inhibition of maternal behavior in the nulliparous female rat. Physiol. Behav. 25, 731-743.
14. Fleming, A.S., Miceli, M., and Moretto, D. (1983). Lesions of the medial preoptic area prevent the facilitation of maternal behavior produced by amygdala lesions. Physiol. Behav. 31, 503-510.
15. Fleming, A.S., Cheung, U.S., and Barry, M. (1990). Cycloheximide blocks the retention of maternal experience in postpartum rats. Behav. Neur. Biol. 53, 64-73.
16. Fleming, A.S., Gavarth, K., and Sarker, J. (1992). Effects of transections to the vomeronasal nerves or to the main olfactory bulbs on the initiation and long-term retention of maternal behavior in primiparous rats. Behav. Neur. Biol. 57, 177-188.
17. Fleming, A.S., Suh, E.J., Korsmit, M., and Rusak, B. (1994). Activation of Fos-like immunoreactivity in the medial preoptic area and limbic structures by maternal and social interactions in rats. Behav. Neurosci. 108, 724-734.
18. Franza, B.R., Rauscher III, F.J., Josephs, S.F., and Curran, T. (1988). The Fos complex and Fos-related antigens recognize sequence elements that contain AP-1 binding sites. Science 239, 1150-1153.
19. Gandelman, R., Zarrow, M.X., Denenberg, V.H., and Myers, M. (1971). Olfactory bulb removal eliminates maternal behavior in the mouse. Science 171, 210-211.
20. Goelet, P., Castellucci, V.F., Schacher, S., and Kandel, E.R. (1986). The long and the short of long-term memory - a molecular framework. Nature 322, 419-422.
21. Griff, I.C., and Reed, R.R. (1995). The genetic basis for specific anosmia to isovaleric acid in the mouse. Cell 83, 407-414.
22. Hai, T., and Curran, T. (1991). Cross-family dimerization of transcription factors Fos/Jun and ATF/CREB alters DNA binding specificity. Proc. Natl. Acad. Sci. USA 88, 3720-3724.
23. Herschman, H.R. (1991). Primary response genes induced by growth factors and tumor promoters. Ann. Rev. Biochem. 60, 281-319.
24. Jirik-Babb, P., Manaker, S., Tucker, A.M., and Hofer, M.A. (1984). The role of the accessory and main olfactory systems in maternal behavior of the primiparous rat. Behav. Neur. Biol. 40, 170-178.
25. Johnson, R.S., Spiegelman, B.M., and Papaioannou, V. (1992). Pleiotropic effects of a null mutation in the c-fos proto-oncogene. Cell 71, 577-586.
26. Kornhauser, J.M., Nelson, D.E., Mayo, K.E., and Takahashi, J.S. (1992). Regulation of JunB messenger RNA and AP-1 activity by light and a circadian clock. Science 255, 1581-1584.
27. Laird, P.W., Zijderveld, A., Linders, K., Rudnicki, M.A., Jaenisch, R., and Berns, A. (1991). Simplified mammalian DNA isolation procedure. Nucleic Acids Res. 19, 4293.
28. Lepri, J.J., Wysocki, C.J., and Vandenbergh, J.G. (1985). Mouse vomeronasal organ: effects on chemosignal production and maternal behavior. Physiol. Behav. 35, 809-814.
29. Lerea, L.S., and McNamara, J.O. (1993). Ionotropic glutamate receptor subtypes activate c-fos transcription by distinct calcium-requiring intracellular signaling pathways. Neuron 10, 31-41.
30. Li, E., Bestor, T.H., and Jaenisch, R. (1992). Targeted mutation of the DNA methyltransferase gene results in embryonic lethality. Cell 69, 915-926.
31. Luckman, S.M. (1995). Fos expression within regions of the preoptic area, hypothalamus and brainstem during pregnancy and parturition. Brain Res. 669, 115-124.
32. Malenfant, S.A., Barry, M., and Fleming, A.S. (1991 ). Effects of cycloheximide on the retention of olfactory learning and maternal experience effects in postpartum rats. Physiol. Behav. 49, 289-294.
33. Mansour, S.L., Thomas, K.R., and Capecchi, M.R. (1988). Disruption of the proto-oncogene Int-2 in mouse embryo-derived stem cells: a general strategy for targeting mutations to non-selectable genes. Nature 336, 348-352.
34. Mumberg, D., Lucibello, F.C., Schuermann, M., and Mueller, R. (1991 ). Alternative splicing of FosB transcripts results in differentially expressed mRNAs encoding functionally antagonistic proteins. Genes Dev. 5, 1212-1223.
35. Nakabeppu, Y., and Nathans, D. (1991). A naturally occurring truncated form of FosB that inhibits Fos/Jun transcriptional activity. Cell 64, 751-759.
36. Noirot, E. (1969a). Changes in responsiveness to young in the adult mouse: V. Priming. Anim. Behav. 17, 542-546.
37. Noirot, E. (1969b). Serial order of maternal responses in mice. Anim. Behav. 17, 547-550.
38. Numan, M. (1994). A neural circuitry analysis of maternal behavior in the rat. Acta Ped. (Suppl.) 397, 19-28.
39. Numan, M., and Numan, M.J. (1995). Importance of pup-related sensory inputs and maternal performance for the expression of Fos-like immunoreactivity in the preoptic area and ventral bed nucleus of the stria terminalis of postpartum rats. Behav. Neurosci. 109, 135-149.
40. Numan, M., Corodimas, K.P., Numan, M.J., Factor, E.M., and Piers, W.D. (1988). Axon-sparing lesions of the preoptic region and substantia innominata disrupt maternal behavior in rats. Behav. Neurosci. 102, 381-396.
41. Orpen, B.G., and Fleming, A.S. (1987). Experience with pups sustains maternal responding in postpartum rats. Physiol. Behav. 40, 47-54.
42. Pedersen, C.A., Ascher, J.A., Monroe, Y.L., and Prange, Jr., A.J. (1982). Oxytocin induces maternal behavior in virgin female rats. Science 216, 648-650.
43. Pedersen, C.A., Caldwell, J.D., Johnson, M.F., Fort, S.A., and Prange, Jr., A.J. (1985). Oxytocin antiserum delays onset of ovarian steroid-induced maternal behavior. Neuropeptides 6, 175-182.
44. Pedersen, C.A., Caldwell, J.D., Walker, C., Ayers, G., and Mason, G.A. (1994). Oxytocin activates the postpartum onset of rat maternal behavior in the ventral tegmental and medial preoptic areas. Behav. Neurosci. 108, 1163-1171.
45. Rauscher III, F.J., Sambucetti, L.C., Curran, T., Distel, R.J., and Spiegelman, B.M. (1988). Common DNA binding site for Fos protein complexes and transcription factor AP-1. Cell 52, 471-480.
46. Robertson, E.J., ed. (1987). Teratocarcinomas and Embryonic Stem Cells: A Practical Approach (Oxford: IRL Press).
47. Rosenblatt, J.S. (1994). Psychobiology of maternal behavior: contribution to the clinical understanding of maternal behavior among humans. Acta Ped. (Suppl.) 397, 3-8.
48. Rosenblatt, J.S., Mayer, A.D., and Giordano, A.L. (1988). Hormonal basis during pregnancy for the onset of maternal behavior in the rat. Psychoneuroendoc. 13, 29-46.
49. Rozen, F., Russo, C., Banville, D., and Zingg, H.H. (1995). Structure, characterization, and expression of the rat oxytocin receptor gene. Proc. Natl. Acad. Sci. USA 92, 200-204.
50. Segal, R.A., and Greenberg, M.E. (1996). Intracellular signalling pathways activated by neurotrophic factors. Annu. Rev. Neurosci. 19, 463-489.
51. Sidis, Y., and Horseman, N.D. (1994). Prolactin induces rapid p95/ p70 tyrosine phosphorylation, and protein binding to GAS-like sites in the Anx Icp35 and c-fos genes. Endocrinology 134, 1979-1985.
52. Smotherman, W.P., Bell, R.W., Starzec, J., and Elias, J. (1974). Maternal responses to infant vocalizations and olfactory cues in rats and mice. Behav. Biol. 12, 55-66.
53. Tybulewicz, V.L.J., Crawford, C.E., Jackson, P.K., Bronson, R.T., and Mulligan, R.C. (1991). Neonatal lethality and lymphopenia in mice with a homozygous disruption of the c-abl proto-oncogene. Cell 65, 1153-1163.
54. Van Leengoed, E., Kerker, E., and Swanson, H.H. (1987). Inhibition of post-partum maternal behavior in the rat by injecting an oxytocin antagonist into the cerebral ventricles. J. Endocr. 112, 275-282.
55. Wang, Z.-Q., Ovitt, C., Grigoriadis, A.E., Moehle-Steinlein, U., Ruether, U., and Wagner, E.F. (1992). Bone and hematopoietic defects in mice lacking c-fos. Nature 360, 741-745.
56. Watanabe, Y., Johnson, R.S., Butler, L.S., Binder, D.K., Spiegelman, B.M., Papaioannou, V.E., and McNamara, J.O. (1996). Null mutation of c-fos impairs structural and functional plasticities in the kindling model of epilepsy. J. Neurosci. 16, 3827-3836.
57. Wisdom, R., and Verma, I.M. (1993). Proto-oncogene FosB: the amino terminus encodes a regulatory function required for transformation. Mol. Cell. Biol. 13, 2635-2643.
58. Wysocki, C.J., Whitney, G., and Tucker, D. (1977). Specific anosmia in the laboratory mouse. Behav. Gen. 7, 171-188.
59. Yen, J., Wisdom, R.M., Tratner, I., and Verma, I.M. (1991). An alternative spliced form of FosB is a negative regulator of transcriptional activation and transformation by Fos proteins. Proc. Natl. Acad. Sci. USA 88, 5077-5081.
60. Zerial, M., Toschi, L., Ryseck, R.-P., Schuermann, M., Mueller, R., and Bravo, R. (1989). The product of a novel growth factor activated gene, FosB, interacts with Jun proteins enhancing their DNA binding activity. EMBO J. 8, 805-813.
61. 2+ channels. Mol. Reprod. Dev. 41, 20-28.