Immunocytochemical evidence for the presence of vasopressin in intermediate sized neurosecretory granules of solitary neurohypophyseal terminals in the homozygous brattleboro rat
A single base deletion (ΔG) in the vasopressin gene is the cause of diabetes insipidus in the homozygous Brattleboro rat (di/di). The resulting frameshift leads to the expression of an aberrant vasopressin precursor which is unable to enter the secretory pathway, thereby preventing vasopressin biosy...
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Published in: | Neuroscience Vol. 72; no. 1; pp. 225 - 231 |
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Abstract | A single base deletion (ΔG) in the vasopressin gene is the cause of diabetes insipidus in the homozygous Brattleboro rat (di/di). The resulting frameshift leads to the expression of an aberrant vasopressin precursor which is unable to enter the secretory pathway, thereby preventing vasopressin biosynthesis. In a small number of solitary magnocellular hypothalamic neurons within the supraoptic and paraventricular nuclei, the reading frame is restored by a dinucleotide (ΔGA) frameshift mutation, at two separate GAGAG motifs downstream of the original G-deletion. This results in two + 1 di-vasopressin precursors that are still partially mutated within the neurophysin region.
The present study provides immunocytochemical evidence which demonstrates that, within magnocellular solitary neurons of the supraoptic and paraventricular nuclei of the di/di rat, the + 1 di-vasopressin precursors can enter the secretory pathway followed by their enzymatic processing into vasopressin during axonal transport to the neural lobe. However, the cellular characteristics of biosynthesis are different from those of wild-type rats. Immunoelectron microscopical localization of vasopressin gene products in the neural lobe of di/di rats revealed their presence in neurosecretory granules, the diameter of which is intermediate (116 nm) between those of the neurosecretory granules in the di/di (80–100 nm) and wild-type (160 nm) rats. |
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AbstractList | A single base deletion (ΔG) in the vasopressin gene is the cause of diabetes insipidus in the homozygous Brattleboro rat (di/di). The resulting frameshift leads to the expression of an aberrant vasopressin precursor which is unable to enter the secretory pathway, thereby preventing vasopressin biosynthesis. In a small number of solitary magnocellular hypothalamic neurons within the supraoptic and paraventricular nuclei, the reading frame is restored by a dinucleotide (ΔGA) frameshift mutation, at two separate GAGAG motifs downstream of the original G-deletion. This results in two + 1 di-vasopressin precursors that are still partially mutated within the neurophysin region.
The present study provides immunocytochemical evidence which demonstrates that, within magnocellular solitary neurons of the supraoptic and paraventricular nuclei of the di/di rat, the + 1 di-vasopressin precursors can enter the secretory pathway followed by their enzymatic processing into vasopressin during axonal transport to the neural lobe. However, the cellular characteristics of biosynthesis are different from those of wild-type rats. Immunoelectron microscopical localization of vasopressin gene products in the neural lobe of di/di rats revealed their presence in neurosecretory granules, the diameter of which is intermediate (116 nm) between those of the neurosecretory granules in the di/di (80–100 nm) and wild-type (160 nm) rats. A single base deletion ( Delta G) in the vasopressin gene is the cause of diabetes insipidus in the homozygous Brattleboro rat (di/di). The resulting frameshift leads to the expression of an aberrant vasopressin precursor which is unable to enter the secretory pathway, thereby preventing vasopressin biosynthesis. In a small number of solitary magnocellular hypothalamic neurons within the supraoptic and paraventricular nuclei, the reading frame is restored by a dinucleotide ( Delta GA) frameshift mutation, at two separate GAGAG motifs downstream of the original G-deletion. This results in two +1 di-vasopressin precursors that are still partially mutated within the neurophysin region. The present study provides immunocytochemical evidence which demonstrates that, within magnocellular solitary neurons of the supraoptic and paraventricular nuclei of the di/di rat, the +1 di-vasopressin precursors can enter the secretory pathway followed by their enzymatic processing into vasopressin during axonal transport to the neural lobe. However, the cellular characteristics of biosynthesis are different from those of wild-type rats. Immunoelectron microscopical localization of vasopressin gene products in the neural lobe of di/di rats revealed their presence in neurosecretory granules, the diameter of which is intermediate (116 nm) between those of the neurosecretory granules in the di/di (80-100 nm) and wild-type (160 nm) rats. A single base deletion (delta G) in the vasopressin gene is the cause of diabetes insipidus in the homozygous Brattleboro rat (di/di). The resulting frameshift leads to the expression of an aberrant vasopressin precursor which is unable to enter the secretory pathway, thereby preventing vasopressin biosynthesis. In a small number of solitary magnocellular hypothalamic neurons within the supraoptic and paraventricular nuclei, the reading frame is restored by a dinucleotide (delta GA) frameshift mutation, at two separate GAGAG motifs downstream of the original G-deletion. This results in two + 1 di-vasopressin precursors that are still partially mutated within the neurophysin region. The present study provides immunocytochemical evidence which demonstrates that, within magnocellular solitary neurons of the supraoptic and paraventricular nuclei of the di/di rat, the + 1 di-vasopressin precursors can enter the secretory pathway followed by their enzymatic processing into vasopressin during axonal transport to the neural lobe. However, the cellular characteristics of biosynthesis are different from those of wild-type rats. Immunoelectron microscopical localization of vasopressin gene products in the neural lobe of did/di rats revealed their presence in neurosecretory granules, the diameter of which is intermediate (116 nm) between those of the neurosecretory granules in the di/di (80-100 nm) and wild-type (160 nm) rats. |
Author | Sonnemans, M.A.F. van Leeuwen, F.W. Evans, D.A.P. Burbach, J.P.H. |
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Cites_doi | 10.1016/0143-4179(94)90057-4 10.1126/science.6648526 10.1016/0306-4522(92)90442-5 10.1016/0306-4522(91)90161-G 10.1016/0196-9781(85)90047-6 10.1210/endo-77-4-701 10.1016/0306-4522(85)90196-4 10.1007/BF00219759 10.1016/0006-8993(86)90272-6 10.1016/0006-8993(94)91456-7 10.1007/BF00217191 10.1002/elps.1150091006 10.1111/j.1432-1033.1989.tb14871.x 10.1016/0006-8993(93)91783-O 10.1523/JNEUROSCI.08-10-03797.1988 10.1016/0006-8993(91)91013-Q 10.1038/308705a0 |
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Keywords | SON DAB diabetes insipidus di supraoptic nucleus PVN neurophysin ER hypothalamus di/di NL paraventricular nucleus Endocrinopathy Animal model Rat Immunocytochemistry Diabetes insipidus Peptide hormone Rodentia Central nervous system Neurosecretory granule Hypothalamus Paraventricular nucleus Gene expression Electron microscopy Neuropeptide Vasopressin Vertebrata Mammalia Animal Hormonal investigation Supraoptic nucleus Brain (vertebrata) |
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References | Valtin, Sawyer, Sokol (bib17) 1965; 77 van Leeuwen, Evans, Meloen, Sonnemans (bib22) 1994; 635 Birch, Hakes, Dixon, Mezey (bib2) 1994; 27 Gainer, Wray (bib8) 1994 van Leeuwen, van der Beek, Seger, Burbach, Ivell (bib20) 1989; 86 van der Sluis, Pool, Sluiter (bib18) 1988; 9 van Leeuwen, Caffé, van der Sluis, Sluiter, van der Woude, Seidah, Chrétien (bib19) 1986; 379 Evans, van der Kleij, Sonnemans, Burbach, van Leeuwen (bib6) 1994; 91 Pow, Morris, Ward (bib11) 1992; 50 Sherman, Watson (bib15) 1988; 8 Chapman, Morris (bib4) 1985; 241 Ivell, Burbach, van Leeuwen (bib10) 1990; 11 Whitnall (bib23) 1983; 222 Whitnall (bib24) 1985; 6 Bertini, Kiss (bib1) 1991; 42 Richards, Morris, Raisman (bib12) 1985; 16 De Bree (bib5) 1995 Swaab, Boer, Nolten (bib16) 1973; 177 Schmale, Borowiak, Holtgreve-Grez, Richter (bib13) 1989; 182 Boersma, Sonnemans, van Leeuwen (bib3) 1993; 611 van Leeuwen, van der Beek (bib21) 1991; 542 Schmale, Richter (bib14) 1984; 308 Guldenaar, Pickering (bib9) 1988; 253 Evans (bib7) 1995 Boersma (10.1016/0306-4522(95)00550-1_bib3) 1993; 611 Birch (10.1016/0306-4522(95)00550-1_bib2) 1994; 27 De Bree (10.1016/0306-4522(95)00550-1_bib5) 1995 Richards (10.1016/0306-4522(95)00550-1_bib12) 1985; 16 Schmale (10.1016/0306-4522(95)00550-1_bib14) 1984; 308 Ivell (10.1016/0306-4522(95)00550-1_bib10) 1990; 11 Sherman (10.1016/0306-4522(95)00550-1_bib15) 1988; 8 van Leeuwen (10.1016/0306-4522(95)00550-1_bib21) 1991; 542 Whitnall (10.1016/0306-4522(95)00550-1_bib23) 1983; 222 Pow (10.1016/0306-4522(95)00550-1_bib11) 1992; 50 van Leeuwen (10.1016/0306-4522(95)00550-1_bib19) 1986; 379 Gainer (10.1016/0306-4522(95)00550-1_bib8) 1994 Schmale (10.1016/0306-4522(95)00550-1_bib13) 1989; 182 Bertini (10.1016/0306-4522(95)00550-1_bib1) 1991; 42 Chapman (10.1016/0306-4522(95)00550-1_bib4) 1985; 241 van der Sluis (10.1016/0306-4522(95)00550-1_bib18) 1988; 9 van Leeuwen (10.1016/0306-4522(95)00550-1_bib22) 1994; 635 Evans (10.1016/0306-4522(95)00550-1_bib6) 1994; 91 Guldenaar (10.1016/0306-4522(95)00550-1_bib9) 1988; 253 Whitnall (10.1016/0306-4522(95)00550-1_bib24) 1985; 6 Valtin (10.1016/0306-4522(95)00550-1_bib17) 1965; 77 van Leeuwen (10.1016/0306-4522(95)00550-1_bib20) 1989; 86 Evans (10.1016/0306-4522(95)00550-1_bib7) 1995 Swaab (10.1016/0306-4522(95)00550-1_bib16) 1973; 177 |
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Snippet | A single base deletion (ΔG) in the vasopressin gene is the cause of diabetes insipidus in the homozygous Brattleboro rat (di/di). The resulting frameshift... A single base deletion (delta G) in the vasopressin gene is the cause of diabetes insipidus in the homozygous Brattleboro rat (di/di). The resulting frameshift... A single base deletion ( Delta G) in the vasopressin gene is the cause of diabetes insipidus in the homozygous Brattleboro rat (di/di). The resulting... |
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SubjectTerms | Animals Base Sequence Biological and medical sciences Cytoplasmic Granules - metabolism diabetes insipidus Diabetes. Impaired glucose tolerance Endocrine pancreas. Apud cells (diseases) Endocrinopathies Etiopathogenesis. Screening. Investigations. Target tissue resistance Female hypothalamus Immunohistochemistry Male Medical sciences Microscopy, Electron Microscopy, Immunoelectron Molecular Sequence Data Mutation neurophysin Neurosecretory Systems - metabolism Neurosecretory Systems - ultrastructure paraventricular nucleus Pituitary Gland, Posterior - metabolism Pituitary Gland, Posterior - ultrastructure Presynaptic Terminals - metabolism Presynaptic Terminals - ultrastructure Rats Rats, Brattleboro Solitary Nucleus - metabolism Solitary Nucleus - ultrastructure supraoptic nucleus Vasopressins - metabolism |
Title | Immunocytochemical evidence for the presence of vasopressin in intermediate sized neurosecretory granules of solitary neurohypophyseal terminals in the homozygous brattleboro rat |
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