TY - JOUR
T1 - Localization of the mRNAs for Two Dopamine D2 Receptor Isoforms in the Rat Brain
AU - Fujiwara, Yutaka
AU - Sora, Ichiro
AU - Tomita, Hiroaki
AU - Akiyama, Kazufumi
AU - Otsuki, Saburo
AU - Yamamura, Henry I.
PY - 1991/12
Y1 - 1991/12
N2 - Abstract: Two molecular forms of the dopamine D., receptor were generated by alternative RNA splicing. To investigate the relative distributions of the two mRNAs encoding the D2 receptor isoforms, D2(415) and D2(444), we performed in situ hybridization histochemistry in the rat brain with the two oligonucleotide probes. An insert probe complementary to an additional fragment of the D, receptor mRNA cloned from the rat brain, and a spanning probe complementary to its contiguous sequence were used. These 48 base probes were 3′‐end labeled with [35S]dATP. The brains were dissected from male SD rats and frozen in dry ice and acetone. Cryostat sections (16 um) were collected on gelatin coated slides and stored at – 20oC. In situ hybridization studies were conducted with a probe concentration of 1 × 10e dpm/100 ^1 of buffer per brain slice at 37oC for 18–20 h in a humid chamber. The slides were washed, dried and exposed to tritium sensitive film for one week. The autoradiograph showed that both mRNA were present at high levels in the corpus striatum, accumbens nucleus and substantia nigra (pars compacta). Identical patterns of labeling were obtained in the rat brain using both the insert and spanning probes, although the optical densities detected with the insert probe were higher than those with the spanning probe in the corpus striatum. This suggests that both D2 receptor mRNAs are expressed similarly in each region of the rat brain and D2(14) expressed dominantly in the corpus striatum.
AB - Abstract: Two molecular forms of the dopamine D., receptor were generated by alternative RNA splicing. To investigate the relative distributions of the two mRNAs encoding the D2 receptor isoforms, D2(415) and D2(444), we performed in situ hybridization histochemistry in the rat brain with the two oligonucleotide probes. An insert probe complementary to an additional fragment of the D, receptor mRNA cloned from the rat brain, and a spanning probe complementary to its contiguous sequence were used. These 48 base probes were 3′‐end labeled with [35S]dATP. The brains were dissected from male SD rats and frozen in dry ice and acetone. Cryostat sections (16 um) were collected on gelatin coated slides and stored at – 20oC. In situ hybridization studies were conducted with a probe concentration of 1 × 10e dpm/100 ^1 of buffer per brain slice at 37oC for 18–20 h in a humid chamber. The slides were washed, dried and exposed to tritium sensitive film for one week. The autoradiograph showed that both mRNA were present at high levels in the corpus striatum, accumbens nucleus and substantia nigra (pars compacta). Identical patterns of labeling were obtained in the rat brain using both the insert and spanning probes, although the optical densities detected with the insert probe were higher than those with the spanning probe in the corpus striatum. This suggests that both D2 receptor mRNAs are expressed similarly in each region of the rat brain and D2(14) expressed dominantly in the corpus striatum.
KW - alternative splicing
KW - dopamine D2 receptor
KW - in situ hybridization
KW - mRNA
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U2 - 10.1111/j.1440-1819.1991.tb00530.x
DO - 10.1111/j.1440-1819.1991.tb00530.x
M3 - Article
C2 - 1813683
AN - SCOPUS:0026346424
SN - 1323-1316
VL - 45
SP - 897
EP - 902
JO - Psychiatry and Clinical Neurosciences
JF - Psychiatry and Clinical Neurosciences
IS - 4
ER -