All vertebrate brains have a cerebellum, and most of them have one or more additional structures that are histologically similar to the cerebellum. The cerebellum-like structures include the medial octavolateral nucleus in most aquatic vertebrates; the dorsal octavolateral nucleus in many aquatic vertebrates with an electrosensory system; the marginal layer of the optic tectum in ray-finned fishes; electrosensory lobes in the few groups of advanced bony fish with an electrosensory system; the rostrolateral nucleus of the thalamus in a few widely scattered groups of bony fish; and the dorsal cochlear nucleus in all mammals except monotremes. All of these structures receive topographically organized sensory input in their deep layers. Purkinje-like cells receive the sensory input near their cell bodies. These cells extend apical dendrites up into the molecular layer where they receive synaptic input from parallel fibers. The cerebellum itself can be included within this characterization by considering the climbing fiber as at least in part a conveyor of sensory information and by recalling that climbing fibers in more basal vertebrates terminate on smooth dendrites close to the soma. Physiological findings from three different systems suggest the hypothesis that cerebellum-like structures remove predictable features from the sensory inflow. Phylogenetic homology can explain the similarities across different taxa for some types of cerebellum-like structures, but similarities within other types cannot be explained in this way. Moreover, phylogenetic homology cannot explain the similarities among different types of cerebellum-like structures. Evolutionary convergence provides the best explanation for all these similarities that cannot be explained by homology. The convergence is almost surely constrained by the availability of a genetic-developmental program for creating cerebellum-like circuitry and by the need within many different systems for the type of information processing that cerebellum-like circuitry can provide.

1.
Acampora, D., V. Avantaggiato, F. Tuorto, and A. Simeone (1997) Genetic control of brain morphogenesis through Otx gene dosage requirement. Development, 124: 3639–3650.
2.
Alvarez-Otero, R., S.D. Regueira, and R. Anadon (1993) New structural aspects of the synaptic contacts on Purkinje cells in an elasmobranch cerebellum. J. Anat., 182: 13–21.
3.
Arshavskii, Y.I., M.B. Berkinblit, I.M. Gel’fand, G.N. Orlovskii, and O.I. Fukson (1972) Activity of the neurones of the ventral spinocerebellar tract during locomotion of cats with deafferentated hind limbs. Biofizika, 17: 1112–1118.
4.
Barmack, N.H., and H. Shojaku (1992) Vestibularly induced slow oscillations in climbing fiber responses of Purkinje cells in the cerebellar nodulus of the rabbit. Neuroscience, 50: 1–5.
5.
Bastian, J. (1986) Electrolocation: Behavior, anatomy, and physiology. In Electroreception (ed. by T.H. Bullock and W. Heiligenberg), Wiley, New York, pp. 577–612.
6.
Bastian, J. (1995) Pyramidal-cell plasticity in weakly electric fish: A mechanism for attenuating responses to reafferent electrosensory inputs. J. Comp. Physiol., 176: 63–78.
7.
Bastian, J. (1999) Plasticity of feedback inputs in the apteronotid electrosensory system. J. Exp. Biol., 202: 1327–1337.
8.
Bell, C.C. (1981a) Central distribution of octavolateral afferents and efferents in a teleost (Mormyridae). J. Comp. Neurol., 195: 391–414.
9.
Bell, C.C. (1981b) Some central connections of medullary octavolateral centers in a mormyrid fish. In Hearing and Sound Communication in Fishes (ed. by R.R. Fay, A.N. Popper and W.N. Tavolga), Springer, New York, pp. 383–392.
10.
Bell, C.C. (1982) Properties of a modifiable efference copy in electric fish. J. Neurophysiol., 47: 1043–1056.
11.
Bell, C.C. (1986) Duration of plastic change in a modifiable efference copy. Brain Res., 369: 29–36.
12.
Bell, C.C. (2001) Memory-based expectations in electrosensory systems. Curr. Opin. Neurobiol., 11: 481–487.
13.
Bell, C.C., and T. Szabo (1986) Electroreception in mormyrid fish: Central anatomy. In Electroreception (ed. by T.H. Bullock and W. Heiligenberg), Wiley, New York, pp. 375–421.
14.
Bell, C., D. Bodznick, J. Montgomery, and J. Bastian (1997a) The generation and subtraction of sensory expectations within cerebellum-like structures. Brain Behav. Evol., 50: 17–31.
15.
Bell, C.C., K. Grant, and J. Serrier (1992) Corollary discharge effects and sensory processing in the mormyrid electrosensory lobe: I. Field potentials and cellular activity in associated structures. J. Neurophysiol., 68: 843–858.
16.
Bell, C.C., V.Z. Han, S. Sugawara, and K. Grant (1997b) Synaptic plasticity in a cerebellum-like structure depends on temporal order. Nature, 387: 278–281.
17.
Berman, N., R.J. Dunn, and L. Maler (2001) Function of NMDA receptors in a feedback pathway of the electrosensory system. J. Neurophysiol., 86: 1612–1621.
18.
Berman, N.J., M.T. Hincke, and L. Maler (1995) Inositol 1,4,5-trisphosphate receptor localization in the brain of a weakly electric fish (Apteronotus leptorhynchus) – with emphasis on the electrosensory system. J. Comp. Neurol., 361: 512–524.
19.
Berrebi, A.S., J.I. Morgan, and E. Mugnaini (1990) The Purkinje cell class may extend beyond the cerebellum. J. Neurocytol., 19: 643–654.
20.
Bodznick, D. (1993) The specificity of an adaptive filter that suppresses unwanted reafference in electrosensory neurons of the skate medulla. Biol. Bull., 185: 312–314.
21.
Bodznick, D., and R.L. Boord (1986) Electroreception in chondrichthyes: Central anatomy and physiology. In Electroreception (ed. by T.H. Bullock and W. Heiligenberg), Wiley, New York, pp. 225–256.
22.
Bodznick, D. and R.G. Northcutt (1980) Segregation of electro- and mechanoreceptive inputs to the elasmobranch medulla. Brain Res., 195: 313–321.
23.
Bodznick, D., J.C. Montgomery, and M. Carey (1999) Adaptive mechanisms in the elasmobranch hindbrain. J. Exp. Biol., 202: 1357–1364.
24.
Bolker, J.A., and R.A. Raff (1996) Developmental genetics and traditional homology. BioEssays, 18: 489–494.
25.
Braford, M.R. (1982) African, but not Asian, notopterid fishes are electroreceptive: Evidence from brain characters. Neuroscience Lett., 32: 35–39.
26.
Bullock, T.H., and W. Heiligenberg (eds.) (1986) Electroreception. Wiley, New York.
27.
Bullock, T.H., D.A. Bodznick, and R.G. Northcutt (1983) The phylogenetic distribution of electroreception: Evidence for convergent evolution of a primitive vertebrate sense modality. Brain Res. Rev., 6: 25–46.
28.
Butler, A.B., and W.M. Saidel (1992) Tectal projection to an unusual nucleus in the diencephalon of a teleost fish, Pantodon buchholzi. Neurosci. Lett., 145: 193–196.
29.
Butler, A.B., and W.M. Saidel (2000) Defining sameness: Historical, biological, and generative homology. BioEssays, 22: 846–853.
30.
Caicedo, A., and H. Herbert (1993) Topography of descending projections from the inferior colliculus to auditory brainstem nuclei in the rat. J. Comp. Neurol., 328: 377–392.
31.
Cajal, S.R. (1952) Histologie du Système Nerveux de l’Homme et des Vertébrés. Instituto Ramon y Cajal, Madrid.
32.
Cant, N.B. (1992) The cochlear nucleus: Neuronal types and their synaptic organization. In The Mammalian Auditory Pathway: Neuroanatomy (ed. by D.B. Webster, A.N. Popper and R.R. Fay), Springer, New York, pp. 66–116.
33.
Carr, C.E., and L. Maler (1986) Electroreception in gymnotiform fish: Central anatomy and physiology. In Electroreception (ed by T.H. Bullock and W. Heiligenberg), Wiley, New York, pp. 319–374.
34.
Conley, R.A., and D. Bodznick (1994) The cerebellar dorsal granular ridge in an elasmobranch has proprioceptive and electroreceptive representations and projects homotopically to the medullary electrosensory nucleus. J. Comp. Physiol. A, 174: 707–721.
35.
Devor, A. (2000) Is the cerebellum like cerebellum-like structures? Brain Res. Rev., 34: 149–156.
36.
Eccles, J., M. Ito, and J. Szentagothai (1967) The Cerebellum as a Neuronal Machine. Springer, New York.
37.
Finger, T.E., and S.L. Tong (1984) Central organization of eighth nerve and mechanosensory lateral line systems in the brainstem of ictalurid catfish. J. Comp. Neurol., 229: 129–151.
38.
Floris, A., M. Dino, D.B. Jacobowitz, and E. Mugnaini (1994) The unipolar brush cells of the rat cerebellar cortex and cochlear nucleus are calretinin-positive: A study by light and electron microscopic immunocytochemistry. Anat. Embryol., 189: 495–520.
39.
Fredette, B.J., and E. Mugnaini (1991) The GABAergic cerebello-olivary projection in the rat. Anat. Embryol., 184: 225–243.
40.
Fujino, K., and D. Oertel (2002) Bidirectional plasticity in the dorsal cochlear nucleus. Assoc. Res. Otolaryngol. Abstr. 31.
41.
Futuyma, D.J. (1998) Evolutionary Biology (3rd ed.). Sinauer, Sunderland, MA.
42.
Gellman, R., A.E. Gibson, and J.C. Houk (1985) Inferior olivary neurons in the awake cat: Detection of contact and passive body displacement. J. Neurophysiol., 54: 40–60.
43.
Hillman, D.E. (1969) Neuronal organization of the cerebellar cortex in amphibia and reptilia. In Neurobiology of Cerebellar Evolution and Development (ed. by R. Llinas), American Medical Association, Chicago, pp. 279–325.
44.
Hjelmstad, G.O., G. Parks, and D. Bodznick (1996) Motor corollary discharge activity and sensory responses related to ventilation in the skate vestibulolateral cerebellum: Implications for electrosensory processing. J. Exp. Biol., 199: 673–681.
45.
Ito, M. (1984) The Cerebellum and Neural Control. Raven Press, New York.
46.
Ito, M. (2001) Cerebellar long-term depression: Characterization, signal transduction, and functional roles. Physiol. Rev., 81: 1143–1195.
47.
Johnson, J.I., J.A. Kirsch, R.L. Reep, and R.C. Switzer (1994) Phylogeny through brain traits: More characters for the analysis of mammalian evolution. Brain Behav. Evol., 43: 319–347.
48.
Kane, E.C. (1974) Synaptic organization in the dorsal cochlear nucleus of the cat: A light and electron microscopic study. J. Comp. Neurol., 155: 301–330.
49.
Kanold, P.O., and E.D. Young (2001) Proprioceptive information from the pinna provides somatosensory input to cat dorsal cochlear nucleus. J. Neurosci., 21: 7848–7858.
50.
Kotchabhakdi, N. (1976) Functional circuitry of the goldfish cerebellum. J. Comp. Physiol. A, 112: 43–73.
51.
Larsell, O. (1967) The Comparative Anatomy and Histology of the Cerebellum from Myxinoids Through Birds. University of Minnesota, Minneapolis, MN.
52.
Lidierth, M., and R. Apps (1990) Gating in the spino-olivocerebellar pathways to the c1 zone of the cerebellar cortex during locomotion in the cat. J. Physiol., 430: 453–469.
53.
Liem, K., W. Bemis, W. Walker, and L. Grande (2001) Functional Anatomy of the Vertebrates: An Evolutionary Perspective. Harcourt, Philadelphia, PA.
54.
Llinas, R., and C. Nicholson (1969) Electrophysiological analysis of alligator cerebellar cortex: A study of dendritic spikes. In Neurobiology of Cerebellar Evolution and Development (ed. by R. Llinas), American Medical Association, Chicago, IL, pp. 431–465.
55.
Llinas, R., and Y. Yarom (1986) Oscillatory properties of guinea-pig inferior olivary neurones and their pharmacological modulation: an in vitro study. J. Physiol., 376: 163–182.
56.
Maeda, N., M. Niinobe, and K. Mikoshiba (1990) A cerebellar Purkinje cell marker P400 protein is an inositol 1,4,5-trisphosphate (InsP3) receptor protein. Purification and characterization of InsP3 receptor complex. EMBO J., 9: 61–67.
57.
Maekawa, K., and J.I. Simpson (1972) Climbing fiber activation of Purkinje cells in the flocculus by impulses transferred through the visual pathway. Brain Res., 39: 245–251.
58.
Maler, L., E.K.B. Sas, and J. Rogers (1981) The cytology of the posterior lateral line lobe of high frequency weakly electric fish (Gymnotidae): Dendritic differentiation and synaptic specificity in a simple cortex. J. Comp. Neurol., 195: 87–140.
59.
Martinez, S., P.H. Crossley, I. Cobos, J.L. Rubenstein, and G.R. Martin (1999) FGF8 induces formation of an ectopic isthmic organizer and isthmocerebellar development via a repressive effect on Otx2 expression. Development, 126: 1189–1200.
60.
McCormick, C.A. (1997) Organization and connections of octaval and lateral line centers in the medulla of a clupeid, Dorosoma cepedianum. Hearing Res., 110: 39–60.
61.
McCormick, C.A. (1999) Anatomy of the central auditory pathways of fish and amphibians. In Comparative Hearing: Fish and Amphibians (ed. by R.R. Fay and A.N. Popper), Springer, New York, pp. 155–217.
62.
McCormick, C.A., and D.V. Hernandez (1996) Connections of octaval and lateral line nuclei of the medulla in the goldfish, including the cytoarchitecture of the secondary octaval population in goldfish and catfish. Brain Behav. Evol., 47: 113–137.
63.
Meek, J. (1992a) Why run parallel fibers parallel? Teleostean Purkinje cells as possible coincidence detectors, in a timing device subserving spatial coding of temporal differences. Neuroscience, 48: 249–283.
64.
Meek, J. (1992b) Comparative aspects of cerebellar organization. Eur. J. Morphol., 30: 37–51.
65.
Meek, J., and R. Nieuwenhuys (1991) Palisade pattern of mormyrid Purkinje cells: A correlated light and electron microscopic study. J. Comp. Neurol., 306: 156–192.
66.
Meek, J., and N.A.M. Schellart (1978) A Golgi study of goldfish optic tectum. J. Comp. Neurol., 182: 89–122.
67.
Meek, J., K. Grant, and C. Bell (1999) Structural organization of the mormyrid electrosensory lateral line lobe. J. Exp. Biol., 202: 1291–1300.
68.
Merzenich, M.M., L. Kitzes, and L. Aitkin (1973) Anatomical and physiological evidence for auditory specialization in the mountain beaver (Aplodontia rufa). Brain Res., 58: 331–344.
69.
Montgomery, J.C., and D. Bodznick (1993) Hindbrain circuitry mediating common mode suppression of ventilatory reafference in the electrosensory system of the little skate Raja erinacea. J. Exp. Biol., 183: 203–215.
70.
Montgomery, J.C., S. Coombs, R.A. Conley, and D. Bodznick (1995) Hindbrain sensory processing in lateral line, electrosensory, and auditory systems: A comparative overview of anatomical and functional similarities. Aud. Neurosci., 1: 207–231.
71.
Mortimer, J.A. (1975) Cerebellar responses to teleceptive stimuli in alert monkeys. Brain Res., 83: 369–390.
72.
Naciemiento, A.C. (1969) Spontaneous and evoked discharges of cerebellar Purkinje cells in the frog. In Neurobiology of Cerebellar Evolution and Development (ed. by R. Llinas), American Medical Association, Chicago, IL, pp. 373–395.
73.
Nelson, M.E., and M.G. Paulin (1995) Neural simulations of adaptive reafference suppression in the elasmobranch electrosensory system. J. Comp. Physiol. A, 177: 723–736.
74.
Nieuwenhuys, R. (1967) Comparative anatomy of the cerebellum. Prog. Brain Res., 25: 1–93.
75.
Nieuwenhuys, R., H.J. Ten Donkelaar, and C. Nicholson (1997) The Central Nervous System of Vertebrates. Springer, Heidelberg.
76.
Northmore, D.P.M., B. Williams, and H. Vanegas (1983) The teleostean torus longitudinalis: Responses related to eye movements, visuotopic mapping, and functional relations with the optic tectum. J. Comp. Physiol. A, 150: 39–50.
77.
Oertel, D., and S.H. Wu (1989) Morphology and physiology of cells in slice preparations of the dorsal cochlear nucleus of mice. J. Comp. Neurol., 283: 228–247.
78.
Paulin, M.G. (1993) The role of the cerebellum in motor control and perception. Brain Behav. Evol., 41: 39–50.
79.
Petralia, R.S., Y.X. Wang, H.M. Zhao, and R.J. Wenthold (1996) Ionotropic and metabotropic glutamate receptors show unique postsynaptic, presynaptic, and glial localizations in the dorsal cochlear nucleus. J. Comp. Neurol., 372: 356–383.
80.
Precht, W., J.I. Simpson, and R. Llinas (1976) Responses of Purkinje cells in rabbit nodulus and uvula to natural vestibular and visual stimuli. Pflügers Arch., 367: 1–6.
81.
Puzdrowski, R.L., and R.B. Leonard (1993) The octavolateral systems in the stingray, Dasyatis sabina. I. Primary projections of the octaval and lateral line nerves. J. Comp. Neurol., 332: 21–37.
82.
Roberts, P.D., and C.C. Bell (2000) Computational consequences of temporally asymmetric learning rules: II. Sensory image cancellation. J. Comput. Neurosci., 9: 67–83.
83.
Robertson, L.T. (1985) Somatosensory representation of the climbing fiber system in the rostral intermediate cerebellum. Exp. Brain Res., 61: 73–86.
84.
Ryugo, D.K., T. Pongstaporn, D.D. Wright, and A.H. Sharp (1995) Inositol 1,4,5-trisphosphate receptors: Immunocytochemical localization in the dorsal cochlear nucleus. J. Comp. Neurol., 358: 102–118.
85.
Saidel, W.M., and A.B. Butler (1997) Visual connections of the atypical diencephalic nucleus rostrolateralis in Pantodon buchholzi (Teleostei, Osteoglossomorpha). Cell Tissue Res., 287: 91–99.
86.
Schmidt, A.W., and D. Bodznick (1987) Afferent and efferent connections of the vestibulolateral cerebellum of the little skate, Raja erinacea. Brain Behav. Evol., 30: 282–302.
87.
Singer, W. (1995) Development and plasticity of cortical processing architectures. Science, 270: 758–764.
88.
Sotelo, C. (1969) Ultrastructural aspects of the cerebellar cortex of the frog. In Neurobiology of Cerebellar Evolution and Development (ed. by R. Llinas), American Medical Association, Chicago, IL, pp. 327–371.
89.
Szabo, T., F. Haugede-Carre, and S. Libouban (1979) Cerebellar afferents in weakly electric mormyrid fish. Neurosci. Lett. Suppl., 3: S144-S144.
90.
Vanegas, H., B. Williams, and J.A. Freeman (1979) Responses to stimulation of marginal fibers in the teleostean optic tectum. Exp. Brain Res., 34: 335–349.
91.
Weedman, D.L., and D.K. Ryugo (1996) Projections from auditory cortex to the cochlear nucleus in rats: Synapses on granule cell dendrites. J. Comp. Neurol., 371: 311–324.
92.
Weinberg, R.J., and A. Rustioni (1987) A cuneocochlear pathway in the rat. Neuroscience, 20: 209–219.
93.
Wolff, A., and H. Kunzle (1997) Cortical and medullary somatosensory projections to the cochlear nuclear complex in the hedgehog tenrec. Neurosci. Lett., 221: 125–128.
94.
Wray, G.A. (2002) Do convergent developmental mechanisms underlie convergent phenotypes? Brain Behav. Evol., 59: 327–336.
95.
Wulliman, M.F. (1994) The teleostean torus longitudinalis: A short review on its structure, histochemistry, connectivity, possible function and phylogeny. Eur. J. Morphol., 32: 235–242.
Copyright / Drug Dosage / Disclaimer
Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher.
Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug.
Disclaimer: The statements, opinions and data contained in this publication are solely those of the individual authors and contributors and not of the publishers and the editor(s). The appearance of advertisements or/and product references in the publication is not a warranty, endorsement, or approval of the products or services advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements.
You do not currently have access to this content.