Cell-specific variation of X chromosome replication in the Syrian hamster (Mesocricetus auratus)

Chromosoma ◽  
1981 ◽  
Vol 84 (3) ◽  
pp. 365-372 ◽  
Author(s):  
A. H. Cawood
Zygote ◽  
2018 ◽  
Vol 26 (2) ◽  
pp. 127-134 ◽  
Author(s):  
Candela Rocío González ◽  
Luciana Moverer ◽  
Ricardo Saúl Calandra ◽  
Silvia Inés González-Calvar ◽  
Alfredo Daniel Vitullo

SummaryThe Deleted in AZoospermia (DAZ) gene family regulates the development, maturation and maintenance of germ cells and spermatogenesis in mammals. The DAZ family consists of two autosomal genes, Boule and Dazl (Daz-like), and the Daz gene on chromosome Y. The aim of this study was to analyze the localization of DAZL and BOULE during testicular ontogeny of the seasonal-breeding Syrian hamster, Mesocricetus auratus. We also evaluated the testicular expression of DAZ family genes under short- or long-photoperiod conditions. In the pre-pubertal and adult testis, DAZL protein was found mainly in spermatogonia. BOULE was found in the spermatogonia from 20 days of age and during the pre-pubertal and adult period it was also detected in spermatocytes and round spermatids. DAZL and BOULE expression in spermatogonia was strictly nuclear only in 20-day-old hamsters. We also detected the novel mRNA and protein expression of BOULE in Leydig cells. In adult hamsters, Dazl expression was increased in regressed testis compared with non-regressed testis and DAZL protein expression was restricted to primary spermatocytes in regressed testis. These results show that DAZL and BOULE are expressed in spermatogonia at early stages in the Syrian hamster, then both proteins translocate to the cytoplasm when meiosis starts. In the adult regressed testis, the absence of DAZL in spermatogonia might be related to the decrease in germ cell number, suggesting that DAZ gene family expression is involved in changes in seminiferous epithelium during photoregression.


1978 ◽  
Vol 12 (4) ◽  
pp. 207-211 ◽  
Author(s):  
E. A. E. Van Marck ◽  
W. Jacob ◽  
A. M. Deelder ◽  
P. L. J. Gigase

Changes in apparently healthy hamsters, consistent with proteinuria, are reported, but no IgG deposits or amyloid in the glomeruli were detected. Further investigation is required into the significance and the aetiology of these, as yet, obscure alterations.


1999 ◽  
Vol 121 (1) ◽  
pp. 89-94 ◽  
Author(s):  
B. Fernández ◽  
A.C. Durán ◽  
A. Martire ◽  
D. López ◽  
V. Sans-Coma

1993 ◽  
Vol 175 (1) ◽  
pp. 53-57 ◽  
Author(s):  
V. Sans-Coma ◽  
J.M. Arqué ◽  
A.C. Durán ◽  
M. Cardo ◽  
B. Fernández ◽  
...  

2001 ◽  
Vol 38 (4) ◽  
pp. 441-446 ◽  
Author(s):  
J. H. Simmons ◽  
L. K. Riley ◽  
C. L. Franklin ◽  
C. L. Besch-Williford

1994 ◽  
Vol 6 (4) ◽  
pp. 533 ◽  
Author(s):  
ES Robinson ◽  
PB Samollow ◽  
JL VandeBerg ◽  
PG Johnston

Somatic cells from the opossums Monodelphis domestica and Didelphis virginiana were labelled with 5-bromodeoxyuridine (BrdU), treated with colchicine, stained with acridine orange and examined using fluorescence microscopy. BrdU-incorporated metaphase spreads from females of M. domestica at developmental stages from late bilaminar blastocysts to adults showed replication asynchrony of the two (acrocentric) X chromosomes. The long arm of one X chromosome was the latest replicating region in the entire chromosome complement and is presumed to represent transcriptional inactivation and X dosage compensation. The minute short arm of the same X, which contains a nucleolar organizer region, was earlier replicating and synchronous with the short arm of its homologue and is thus assumed to escape inactivation. BrdU-incorporated spreads from cells of fetuses, neonates and adults of D. virginiana also showed a late replicating (submetacentric) X chromosome. The pattern was different from that of M. domestica because of the different morphology and the presence of large blocks of constitutive heterochromatin in both homologues. The timing and pattern of replication of the single X in males of both species resembled the earlier replicating X in females. The array of molecular techniques now available offers the best means for investigating X-chromosome replication and activity states of X-linked genes in the earliest stages of marsupial embryogenesis.


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