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Sterol Carrier Protein 2 OKDB#: 334
 Symbols: SCP2 Species: human
 Synonyms: SCP2  Locus: 1p32 in Homo sapiens


For retrieval of Nucleotide and Amino Acid sequences please go to: OMIM Entrez Gene
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General Comment The intracellular movement of cholesterol is an important regulated step in the process of steroidogenesis. Lipid transfer proteins may have an important function in this process. One candidate lipid transfer protein is sterol carrier protein 2 (SCP2). This 13.2 kDa protein enhances the movement of cholesterol between vesicles and isolated mitochondria. It also stimulates mitochondrial pregnenolone synthesis. SCP2 is abundant in steroidogenic glands and the pattern of SCP2 gene expression is consistent with a role for the protein in hormone synthesis: SCP2 transcripts are more prominent in the most steroidogenic compartments of the ovary and tropic hormones that stimulate steroidogenesis increase SCP2 gene expression. The protein appears to bind sterols and is synthesized with a 20 amino acid N-terminal "pro-" sequence that may serve to target SCP2 to mitochondria. In addition, the C-terminus of SCP2 contains a peroxisome-targeting sequence. Diseases of peroxisome function, including adrenoleukodystrophy and Zellweger syndrome, have notable deficits in steroid and bile acid metabolism, thus linking peroxisomes and steroidogenesis. SCP2 is deficient in fibroblasts of patients with these diseases (Pfeifer et al., 1993).

General function
Comment See Pfeifer et al., 1993
Cellular localization Mitochondrial
Comment See Pfeifer et al., 1993
Ovarian function Steroid metabolism
Comment See Pfeifer et al., 1993
Expression regulated by LH, Steroids, cAMP
Comment
Ovarian localization Granulosa, Theca, Luteal cells
Comment In situ hybridization revealed that the most steroidogenically active ovarian compartments (e.g., corpora lutea and theca cells) contain significant amounts of SCP2 mRNA whereas granulosa cells have modest levels. (Rennert et al., 1991)
Follicle stages Primary, Secondary, Antral, Preovulatory, Corpus luteum
Comment To investigate the coordinate developmental expression of sterol carrier protein 2 (SCP2) throughout the pig estrous cycle, RNase protection analysis was performed using homologous (partially cloned) porcine sequences. Specific transcripts (relative to 18S rRNA) were quantified in immature ovaries, preovulatory follicles (> or = 5 mm), corpora lutea (CL), and corpora albicantia. Expression of SCP2 mRNA did not differ among the four tissue types but tended to be highest in midcycle (Day 12) CL compared other stages of CL (p = 0.007). In summary, P450scc and StAR message expression are coordinately amplified during the pig follicular and luteal phase, whereas LDL receptor message after an initial increase is expressed at constitutively high levels, thus indicating a differential regulation of ovarian sterol-metabolizing genes during the steroidogenic life of the follicle and CL. (LaVoie et al., 1997)
Phenotypes
Mutations 1 mutations

Species: rat
Mutation name: None
type: null mutation
fertility: None
Comment: Gene targeting in mice was used to investigate the unknown function of Scp2, encoding sterol carrier protein-2. Complete deficiency of SCP2 and SCPx was associated with marked alterations in gene expression, peroxisome proliferation, hypolipidemia, impaired body weight control, and neuropathy. Along with these abnormalities, catabolism of methyl-branched fatty acyl CoAs was impaired. The defect became evident from up to 10-fold accumulation of the tetramethyl-branched fatty acid phytanic acid in Scp2(-/-) mice. Further characterization supported that the gene disruption led to inefficient import of phytanoyl-CoA into peroxisomes and to defective thiolytic cleavage of 3-ketopristanoyl-CoA. (Seedorf et al., 1998)

Genomic Region show genomic region
Phenotypes and GWAS show phenotypes and GWAS
Links
OMIM (Online Mendelian Inheritance in Man: an excellent source of general gene description and genetic information.)
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created: Dec. 11, 1999, midnight by: Pau   email:
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last update: Aug. 9, 2006, 3:29 p.m. by: Alex    email:



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