Rat endozepine-like peptide (ELP): cDNA cloning, genomic organization and tissue-specific expression.

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Rat endozepine-like peptide (ELP): cDNA cloning, genomic organization and tissue-specific expression. / Schulze, Wolfgang; Jähner, D; Spiess, Andrej-Nikolai; Ivell, R.

in: GENE, Jahrgang 235, Nr. 1-2, 1-2, 1999, S. 51-57.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

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Schulze W, Jähner D, Spiess A-N, Ivell R. Rat endozepine-like peptide (ELP): cDNA cloning, genomic organization and tissue-specific expression. GENE. 1999;235(1-2):51-57. 1-2.

Bibtex

@article{0666be8142eb4a6e8e59534e5ddb51ee,
title = "Rat endozepine-like peptide (ELP): cDNA cloning, genomic organization and tissue-specific expression.",
abstract = "A cDNA encoding the rat homolog of the previously characterized murine endozepine-like peptide (ELP) was isolated by a PCR cloning strategy. Sequence comparison with the murine cDNA sequence revealed a conservation of the ELP primary structure between both rodent species with minor amino acid exchanges. We investigated the genomic organization of the rat ELP gene by genomic PCR. This indicated the presence of a single short intron of 451bp interrupting the 5' untranslated region. Tissue-dependent ELP expression was determined by Northern hybridization and semiquantitative RT-PCR. Northern hybridization showed an ELP specific transcript in both the male and the female gonad, but the level of ovarian ELP transcription was considerably lower than in the testis. RT-PCR analysis demonstrated a low and varying level of ELP background expression in all examined tissues. In contrast to the closely related ACBP gene, ELP shows a different genomic organization and a more regulated expression pattern, and may exert a specific function as a gonadal acyl-CoA pool former and transporter.",
author = "Wolfgang Schulze and D J{\"a}hner and Andrej-Nikolai Spiess and R Ivell",
year = "1999",
language = "Deutsch",
volume = "235",
pages = "51--57",
journal = "GENE",
issn = "0378-1119",
publisher = "Elsevier",
number = "1-2",

}

RIS

TY - JOUR

T1 - Rat endozepine-like peptide (ELP): cDNA cloning, genomic organization and tissue-specific expression.

AU - Schulze, Wolfgang

AU - Jähner, D

AU - Spiess, Andrej-Nikolai

AU - Ivell, R

PY - 1999

Y1 - 1999

N2 - A cDNA encoding the rat homolog of the previously characterized murine endozepine-like peptide (ELP) was isolated by a PCR cloning strategy. Sequence comparison with the murine cDNA sequence revealed a conservation of the ELP primary structure between both rodent species with minor amino acid exchanges. We investigated the genomic organization of the rat ELP gene by genomic PCR. This indicated the presence of a single short intron of 451bp interrupting the 5' untranslated region. Tissue-dependent ELP expression was determined by Northern hybridization and semiquantitative RT-PCR. Northern hybridization showed an ELP specific transcript in both the male and the female gonad, but the level of ovarian ELP transcription was considerably lower than in the testis. RT-PCR analysis demonstrated a low and varying level of ELP background expression in all examined tissues. In contrast to the closely related ACBP gene, ELP shows a different genomic organization and a more regulated expression pattern, and may exert a specific function as a gonadal acyl-CoA pool former and transporter.

AB - A cDNA encoding the rat homolog of the previously characterized murine endozepine-like peptide (ELP) was isolated by a PCR cloning strategy. Sequence comparison with the murine cDNA sequence revealed a conservation of the ELP primary structure between both rodent species with minor amino acid exchanges. We investigated the genomic organization of the rat ELP gene by genomic PCR. This indicated the presence of a single short intron of 451bp interrupting the 5' untranslated region. Tissue-dependent ELP expression was determined by Northern hybridization and semiquantitative RT-PCR. Northern hybridization showed an ELP specific transcript in both the male and the female gonad, but the level of ovarian ELP transcription was considerably lower than in the testis. RT-PCR analysis demonstrated a low and varying level of ELP background expression in all examined tissues. In contrast to the closely related ACBP gene, ELP shows a different genomic organization and a more regulated expression pattern, and may exert a specific function as a gonadal acyl-CoA pool former and transporter.

M3 - SCORING: Zeitschriftenaufsatz

VL - 235

SP - 51

EP - 57

JO - GENE

JF - GENE

SN - 0378-1119

IS - 1-2

M1 - 1-2

ER -