scholarly journals Sexual Development Dysgenesis in Interspecific Hybrids of Rice Fish

Author(s):  
Anabel Martinez-Bengochea ◽  
Susanne Kneitz ◽  
Amaury Herpin ◽  
Rafael Henrique Nóbrega ◽  
Mateus C. Adolfi ◽  
...  

Abstract Fish are amongst vertebrates the group with the highest diversity of known sex-determining genes. Particularly, the genus Oryzias is a suitable taxon to understand how different sex determination genetic networks evolved in closely related species. Two closely related species, O. latipes and O. curvinotus, do not only share the same XX/XY sex chromosome system, but also the same male sex-determining gene, dmrt1bY. We performed whole mRNA transcriptomes and morphology analyses of the gonads of hybrids resulting from reciprocal crosses between O. latipes and O. curvinotus. XY male hybrids, presenting meiotic arrest and no production of sperm were sterile, and about 30% of the XY hybrids underwent male-to-female sex reversal. Both XX and XY hybrid females exhibited reduced fertility and developed ovotestis while aging. Transcriptome data showed that male-related genes are upregulated in the XX and XY female hybrids. The transcriptomes of both types of female and of the male gonads are characterized by upregulation of meiosis and germ cell differentiation genes. Differences in the parental species in the downstream pathways of sexual development could explain sex reversal, sterility, and the development of intersex gonads in the hybrids. Our results provide molecular clues for the proximate mechanisms of hybrid incompatibility and Haldane’s rule.

1966 ◽  
Vol 14 (5) ◽  
pp. 821 ◽  
Author(s):  
MJD White ◽  
J Cheney

Two closely related species belonging to the cultrata group show an XY condition in the male as a result of an X-autosome fusion. One of these has two cytological races which differ in the shape of the Y chromosome. This complex of XY forms has given rise to an XlX2Y species by a further Y-autosome fusion. The latter species has two cytological races which differ in the shape of the Y and X2 chromosomes, presumably as a result of the fixation of pericentric inversions and other structural changes.


Behaviour ◽  
2015 ◽  
Vol 152 (3-4) ◽  
pp. 407-423 ◽  
Author(s):  
Victoria Wobber ◽  
Esther Herrmann

Levels of the steroid hormone testosterone have been found to impact diverse features of cognition from spatial memory to decision-making regarding risk, both in humans and other animals. However less is known about whether closely-related species differ in their testosterone-cognition relationships in line with pressures shaping each species’ cognitive evolution. We therefore examined relationships between testosterone and cognition in two-closely related species that differ markedly in their social behaviour, cognition, and patterns of testosterone production: bonobos (Pan paniscus) and chimpanzees (Pan troglodytes). We presented individuals of both species with a battery of 16 cognitive tasks and determined whether performance on these tasks correlated with average testosterone level. We found that among male chimpanzees, high levels of testosterone correlated with higher performance in numerous tasks, including tasks assessing spatial cognition and physical cognitive abilities more broadly. Meanwhile, in male bonobos we found no correlations between testosterone and performance on the cognitive tasks, and found no correlations in females of either species. Building on prior comparative research, these results suggest that bonobos and chimpanzees differ critically in the proximate mechanisms influencing their cognitive capacities, and that in particular the role of testosterone in shaping behaviour and cognition differs dramatically between the two species.


2020 ◽  
Vol 9 (3) ◽  
pp. 160-170
Author(s):  
Thumadath P.A. Krishna ◽  
Maharajan Theivanayagam ◽  
Gurusunathan V. Roch ◽  
Veeramuthu Duraipandiyan ◽  
Savarimuthu Ignacimuthu

Finger millet is a superior staple food for human beings. Microsatellite or Simple Sequence Repeat (SSR) marker is a powerful tool for genetic mapping, diversity analysis and plant breeding. In finger millet, microsatellites show a higher level of polymorphism than other molecular marker systems. The identification and development of microsatellite markers are extremely expensive and time-consuming. Only less than 50% of SSR markers have been developed from microsatellite sequences for finger millet. Therefore, it is important to transfer SSR markers developed for related species/genus to finger millet. Cross-genome transferability is the easiest and cheapest method to develop SSR markers. Many comparative mapping studies using microsatellite markers clearly revealed the presence of synteny within the genomes of closely related species/ genus. Sufficient homology exists among several crop plant genomes in the sequences flanking the SSR loci. Thus, the SSR markers are beneficial to amplify the target regions in the finger millet genome. Many SSR markers were used for the analysis of cross-genome amplification in various plants such as Setaria italica, Pennisetum glaucum, Oryza sativa, Triticum aestivum, Zea mays and Hordeum vulgare. However, there is very little information available about cross-genome amplification of these markers in finger millet. The only limited report is available for the utilization of cross-genome amplified microsatellite markers in genetic analysis, gene mapping and other applications in finger millet. This review highlights the importance and implication of microsatellite markers such as genomic SSR (gSSR) and Expressed Sequence Tag (EST)-SSR in cross-genome analysis in finger millet. Nowadays, crop improvement has been one of the major priority areas of research in agriculture. The genome assisted breeding and genetic engineering plays a very crucial role in enhancing crop productivity. The rapid advance in molecular marker technology is helpful for crop improvement. Therefore, this review will be very helpful to the researchers for understanding the importance and implication of SSR markers in closely related species.


Genetics ◽  
2004 ◽  
Vol 166 (2) ◽  
pp. 789-796 ◽  
Author(s):  
Kyoichi Sawamura ◽  
John Roote ◽  
Chung-I Wu ◽  
Masa-Toshi Yamamoto

Abstract Recent genetic analyses of closely related species of Drosophila have indicated that hybrid male sterility is the consequence of highly complex synergistic effects among multiple genes, both conspecific and heterospecific. On the contrary, much evidence suggests the presence of major genes causing hybrid female sterility and inviability in the less-related species, D. melanogaster and D. simulans. Does this contrast reflect the genetic distance between species? Or, generally, is the genetic basis of hybrid male sterility more complex than that of hybrid female sterility and inviability? To clarify this point, the D. simulans introgression of the cytological region 34D-36A to the D. melanogaster genome, which causes recessive male sterility, was dissected by recombination, deficiency, and complementation mapping. The 450-kb region between two genes, Suppressor of Hairless and snail, exhibited a strong effect on the sterility. Males are (semi-)sterile if this region of the introgression is made homozygous or hemizygous. But no genes in the region singly cause the sterility; this region has at least two genes, which in combination result in male sterility. Further, the males are less fertile when heterozygous with a larger introgression, which suggests that dominant modifiers enhance the effects of recessive genes of male sterility. Such an epistatic view, even in the less-related species, suggests that the genetic complexity is special to hybrid male sterility.


Sign in / Sign up

Export Citation Format

Share Document