ApoA-I-binding protein (AI-BP) and its homologues hYjeF_N2 and hYjeF_N3 comprise the YjeF_N domain protein family in humans with a role in spermiogenesis and oogenesis

Rudolph, C. and Sigruener, A. and Hartmann, A. and Orso, E. and Bals-Pratsch, M. and Gronwald, W. and Seifert, B. and Kalbitzer, Hans Robert and Verdorfer, I. and Luetjens, C. M. and Ortmann, O. and Bornstein, S. R. and Schmitz, G. (2007) ApoA-I-binding protein (AI-BP) and its homologues hYjeF_N2 and hYjeF_N3 comprise the YjeF_N domain protein family in humans with a role in spermiogenesis and oogenesis. Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et métabolisme 39 (5), pp. 322-335.

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Abstract

The screening for additional human YjeF_N domain containing proteins beside the apolipoprotein A-I interacting protein (AI-BP), identified two other genes designated hYjeF_N2-15q23 (formerly human homologue of yeast edc3) and hYjeF_N3-19p13.11 comprising the human YjeF_N family. AI-BP is ubiquitously expressed, with a predominance of these tissues where the homologues were found to be restricted including brain, mammary gland, testes and ovaries. Immunohistochemistry of human testes and ovaries showed an expression of hYjeF_N3-19p13.11 only in Leydig cells and theca cells, respectively, indicating a role in steroid hormone metabolism. Interestingly, the protein was also strongly expressed in Leydig cell tumors and in thecofibromas. The identification of hYjeF_N2-15q23 in theca cells and granulosa cells in ovaries, in human spermatids of meiotic division part II and the apical membrane of Sertoli cells in testes suggest similar functions in oogenesis and sperm maturation which is strengthened by the identification of the spermatogenesis regulator HMGA1 as a conserved transcription factor. However, in contrast to AI-BP, both homologous proteins are unable to bind apoA-I. These results relate the human YjeF_N domain containing protein family to cholesterol processing and steroid hormone metabolism in spermiogenesis and oogenesis, and AI-BP may link this function to the HDL pathway.

Item Type:Article
Institutions: Biology, Preclinical Medicine > Institut für Biophysik und physikalische Biochemie > Prof. Dr. Dr. Hans Robert Kalbitzer
Identification Number:
ValueType
17533573PubMed ID
10.1055/s-2007-977699DOI
Classification:
NotationType
AdultMESH
AgedMESH
Aged, 80 and overMESH
Amino Acid SequenceMESH
Blotting, NorthernMESH
Blotting, WesternMESH
Carrier Proteins/physiologyMESH
Child, PreschoolMESH
DNA ProbesMESH
DNA, Complementary/geneticsMESH
FemaleMESH
Fibroma/pathologyMESH
Genome, HumanMESH
HumansMESH
ImmunohistochemistryMESH
Leydig Cell Tumor/pathologyMESH
Lipoproteins, HDL/physiologyMESH
MaleMESH
Middle AgedMESH
Molecular Sequence DataMESH
Oogenesis/physiologyMESH
Ovary/cytologyMESH
Pregnancy Proteins/physiologyMESH
Promoter Regions, Genetic/geneticsMESH
RNA/geneticsMESH
Reverse Transcriptase Polymerase Chain ReactionMESH
Spermatogenesis/physiologyMESH
Testicular Neoplasms/pathologyMESH
Testis/cytologyMESH
Subjects:500 Science > 570 Life sciences
Status:Published
Refereed:Unknown
Created at the University of Regensburg:Unknown
Owner:Gertraud Kellers
Deposited On:17 Sep 2010 09:27
Last Modified:17 Sep 2010 09:27
Item ID:16657
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