scholarly journals On the Chromosome Number and the Sex-chromosomes in the Germ-cells of Male and Female Cats

CYTOLOGIA ◽  
1934 ◽  
Vol 5 (3) ◽  
pp. 355-362 ◽  
Author(s):  
Osamu Minouchi ◽  
Takeo Ohta
Genome ◽  
1996 ◽  
Vol 39 (4) ◽  
pp. 818-821 ◽  
Author(s):  
G. Röder ◽  
K. E. Linsenmair ◽  
I. Nanda ◽  
M. Schmid

The karyotype of male and female Hemilepistus elongatus was investigated by means of C-banding. The diploid chromosome number in both sexes is 2n = 50. By scrutinizing general morphology and localization of the constitutive heterochromatin, no heteromorphic sex chromosomes were found. All chromosome pairs in males are well paired during diakinesis. Hybridization of genomic DNA with (GACA)4 and (GATA)4 oligonucleotides revealed no sex-specific patterns. Key words : karyotype, C-banding, sex determination, simple DNA-repeats, Isopoda.


1984 ◽  
Vol 26 (1) ◽  
pp. 100-103 ◽  
Author(s):  
J. A. Adegoke

The chromosomes of Mabuya blandingi were studied from the bone marrow of male and female animals. The diploid chromosome number in this organism is 32, consisting of 10 large-, 10 medium-, and 12 small-size chromosomes. The fundamental number (NF) is 48. The chromosome complements in both the male and female animals are similar in morphology with no evidence of differentiated sex chromosomes.


1925 ◽  
Vol 8 (2) ◽  
pp. 1-20 ◽  
Author(s):  
Charles L. Parmenter

1. This paper presents cytological observations upon Dr. Loeb's parthenogenetic frog material, with considerations upon the mechanism by which the diploid number and both sexes may be produced. 2. Both sexes of adults and tadpoles are present. 3. The chromosome number is diploid and probably 26 in both sexes. Sex chromosomes cannot be distinguished. 4. The chromosome numbers observed by other authors in parthenogenetic frog material are haploid, diploid, and variable. Their significance is considered. 5. The mechanism producing the diploid number, based on European observations, appears to be a doubling of the haploid number at some time after the second polar body is given off. 6. Overripeness may be a factor in producing both sexes of parthenogenetic frogs and tadpoles. 7. Genetic data indicate that the normal male is digametic and that there are differences of potency between male and female factors for sex which vary in frogs of the two races and in strains within the race. These differences have been interpreted by Witschi as forming a series of multiple allelomorphs.


Genetics ◽  
1997 ◽  
Vol 147 (1) ◽  
pp. 231-242 ◽  
Author(s):  
Lucas Sánchez ◽  
Pedro Santamaria

Abstract This article reports the breaking of ethological barriers through the constitution of soma-germ line chimeras between species of the melanogaster subgroup of Drosophila, which are ethologically isolated. Female Drosophila yakuba and D. teissieri germ cells in a D. melanogaster ovary produced functional oocytes that, when fertilized by D. melanogaster sperm, gave rise to sterile yakuba-melanogaster andteissieri-melanogaster male and female hybrids. However, the erecta-melanogaster and orena-melanogaster hybrids were lethal, since female D. erecta and D. orena germ cells in a D. melanogaster ovary failed to form oocytes with the capacity to develop normally. This failure appears to be caused by an altered interaction between the melanogaster soma and the erecta and orena germ lines. Germ cells of D. teissieri and D. orena in a D. melanogaster testis produced motile sperm that was not stored in D. melanogaster females. This might be due to incompatibility between the teissieri and orena sperm and the melanogaster seminal fluid. A morphological analysis of the terminalia of yakuba-melanogaster and teissieri-melanogaster hybrids was performed. The effect on the terminalia of teissieri-melanogaster hybrids of a mutation in doublesex, a regulatory gene that controls the development of the terminalia, was also investigated.


2001 ◽  
Vol 78 (1) ◽  
pp. 23-30 ◽  
Author(s):  
MARIKO KONDO ◽  
ERIKO NAGAO ◽  
HIROSHI MITANI ◽  
AKIHIRO SHIMA

In the medaka, Oryzias latipes, sex is determined chromosomally. The sex chromosomes differ from those of mammals in that the X and Y chromosomes are highly homologous. Using backcross panels for linkage analysis, we mapped 21 sequence tagged site (STS) markers on the sex chromosomes (linkage group 1). The genetic map of the sex chromosome was established using male and female meioses. The genetic length of the sex chromosome was shorter in male than in female meioses. The region where male recombination is suppressed is the region close to the sex-determining gene y, while female recombination was suppressed in both the telomeric regions. The restriction in recombination does not occur uniformly on the sex chromosome, as the genetic map distances of the markers are not proportional in male and female recombination. Thus, this observation seems to support the hypothesis that the heterogeneous sex chromosomes were derived from suppression of recombination between autosomal chromosomes. In two of the markers, Yc-2 and Casp6, which were expressed sequence-tagged (EST) sites, polymorphisms of both X and Y chromosomes were detected. The alleles of the X and Y chromosomes were also detected in O. curvinotus, a species related to the medaka. These markers could be used for genotyping the sex chromosomes in the medaka and other species, and could be used in other studies on sex chromosomes.


Development ◽  
1980 ◽  
Vol 55 (1) ◽  
pp. 53-63
Author(s):  
V. Gremigni ◽  
C. Miceli ◽  
I. Puccinelli

Specimens from a polyploid biotype of Dugesia lugubris s.l. were used to clarify the role and fate of germ cells during planarian regeneration. These specimens provide a useful karyological marker because embryonic and somatic cells (3n = 12) can be easily distinguished from male (2n = 8) and female (6n = 24) germ cells by their chromosome number. We succeed in demonstrating how primordial germ cells participate in blastema formation and take part in rebuilding somatic tissues. This evidence was obtained by cutting each planarian specimen twice at appropriate levels. The first aimed to induce primordial germ cells to migrate to the wound. The second cut was performed after complete regeneration and aimed to obtain a blastema from a cephalic or caudal area devoid of gonads. A karyological analysis of mitotic cells present in each blastema obtained after the second cut provided evidence that cells, originally belonging to the germ lines, are still present in somatic tissues even months after complete regeneration. The role of primordial germ cells in planarian regeneration was finally discussed in relation to the phenomenon of metaplasia or transdifferentiation.


1994 ◽  
Vol 72 (6) ◽  
pp. 1100-1119 ◽  
Author(s):  
B. S. Heming ◽  
E. Huebner

Newly deposited eggs of Rhodnius prolixus lack a visible pole plasm and require 14 days to develop at 27 °C and 70% RH. The first germ cells originate at 9% of embryogenesis by asynchronous mitosis of blastodermal cells behind the germ Anlage at the posterior pole of the egg. From 9 to 17%, these proliferate to a mean of 270 cells and, from 13 to 18%, migrate forward over the dorsal surface of the mesoderm and lodge in abdominal segments 3–7. Between 22 and 30%, they shift laterally and segregate into three or four paired clumps between segments 3 and 4, 4 and 5, 5 and 6, and, sometimes, 6 and 7 and, from 30 to 37%, gradually assemble into a continuous longitudinal mass on either side of segments 3–6, where they begin to associate with mesodermal cells. Between 37 and 46%, these collect between (males) and around the germ cells to form the rudiments of the terminal filaments (females), inner and outer gonadal sheaths, interstitial cells (males), and primary exit ducts. Dorsally situated sheath cells then invaginate ventrally into each gonadal rudiment, partitioning it into seven compartments, each containing a mean of 15 oogonia or 16 spermatogonia. These seem to fuse into a rosette, at least in females, but do not begin to divide again until after hatch. Excluded germ cells lodge within the rudiments of one or both exit ducts. The evolutionary and functional aspects of our findings are addressed and new observations are presented on the mechanism of anatrepsis.


2011 ◽  
Vol 25 (9) ◽  
pp. 959-971 ◽  
Author(s):  
Y. Ichijima ◽  
M. Ichijima ◽  
Z. Lou ◽  
A. Nussenzweig ◽  
R. D. Camerini-Otero ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document