mRNA
expression pattern of multiple members of connexin gene family
in normal and abnormal fetal gonads in mouse*
Subhash C. Juneja
Departments of Zoology,
The University of Western Ontario,
London, Ontario, Canada N6A 5C1
( Received on September 18,
2002 )
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Abstract
Gap junctions are made of connexin
(Cx) molecules and provide communications between adjacent
cells through which small molecules (<1kDa) move between
cytoplasms. The connexin gene family consists of at least
17 members. Gap junctions play important roles in ovarian
and testicular function. Connexin 43 (Cx43) knockout mouse
is a model for developmentally impaired fetal gonads. The
aim of the current study was twofold : (a) to analyze mRNA
expression pattern of multiple members of connexin gene family
in normal fetal gonads; (b) to investigate any alteration
of mRNA expression of connexins in developmentally impaired
fetal gonads. The study was conducted in normal gonads obtained
from 17.5 dpc wildtype (Cx43+/+) and heterozygote (Cx43+/)
fetuses and in developmentally impaired gonads obtained from
17.5 dpc knockout (Cx43/) fetuses. The mRNA expression
pattern of connexins (Cx26, Cx30.3, Cx31, Cx31.1, Cx32, Cx37,
Cx40, Cx43, Cx45, Cx46 and Cx50) was analyzed by RT-PCR. The
mRNA transcripts for Cx32 and Cx50 were absent in fetal testis
of all the genotypes, and the transcripts for Cx26, Cx30.3,
Cx31.1, Cx32, Cx40, Cx46 and Cx50 were absent in fetal ovary
of all the genotypes. The transcripts for Cx43 showed expression
in Cx43+/+ and Cx43+/ gonads and were absent in Cx43/
gonads, as expected. Additionally, the mRNA transcripts for
8 more connexins (Cx26, Cx30.3, Cx31, Cx31.1, Cx37, Cx40,
Cx45 and Cx46) showed expression in Cx43+/+ and Cx43+/
fetal testes, but the transcripts for only 4 connexins (Cx26,
Cx37, Cx40 and Cx45) showed expression in Cx43/
fetal testis. In fetal ovary, the mRNA transcripts for 3 more
connexins (Cx31, Cx37 and Cx45) were expressed in all the
genotypes. In summary, from the mRNA expression analysis of
11 members of connexin gene family in 17.5 dpc fetal gonads,
besides the expression of Cx43, 8 additional connexins were
expressed in normal fetal testis but only 4 connexins were
expressed in developmentally impaired testis. The fetal ovary
showed the expression of 3 additional connexins besides the
expression of Cx43. In developmentally impaired fetal ovary,
only Cx43 was not expressed as expected but other three connexins
were expresed. The study may be useful in interpreting human
testis defects in infertility cases.