S. Zimmermann et al., MOUSE LEYDIG INSULIN-LIKE (LEY I-L) GENE - STRUCTURE AND EXPRESSION DURING TESTIS AND OVARY DEVELOPMENT, Molecular reproduction and development, 47(1), 1997, pp. 30-38
Leydig insulin-like protein (Ley I-L) is a novel member of the insulin
-like hormone superfamily. We report here the isolation and expression
of the mouse Ley I-L gene. The gene encodes a polypeptide of 122 amin
o acids that shows a relatively weak homology (54%) to human and porci
ne prepro-Ley I-L. However, the predicted B and A chain of the mature
mouse Ley I-L exhibit similarities of 73% and 71% with human and porci
ne Ley I-L, respectively, Alignment of the 5' flanking region of the m
ouse gene with those of human and porcine did not exhibit any signific
ant sequence homology. However, it contains the conserved sequence of
the Ad4 binding site that is present in all promoter regions of steroi
dogenic P-450 genes and the Mullerian inhibitor substance gene and is
recognized by steroidogenic factor 1. The Ley I-L gene is expressed at
a high level in the testis and at a much lower level in the ovary. No
transcripts could be detected in placenta prepared between days 10 an
d 19 of pregnancy. Ley I-L transcripts were first detected in fetal te
stis at 13.5 dpc. After birth, transcript levels remain constant durin
g the following 3 weeks, increasing at the stage in which the first wa
ve of round spermatids undergo spermiogenesis suggesting a functional
role of the Ley I-L in early stages of spermatogenesis and germ-cell m
aturation. In the ovary, the expression of Ley I-L was first detected
at day 6 after birth. The pattern of Ley I-L expression at various sta
ges of the estrous cycle and during pregnancy showed a correlation wit
h follicle development. (C) 1997 Wiley-Liss, Inc.