Meiosis of four telocentric-tertiary compensating trisomics of rye (Secale cereale L.) was studied with the purpose of evaluating their suitability for use in maintaining genic male-sterile lines applied in hybrid varieties. They had been constructed from four different reciprocal translocations and three different telocentrics. In one trisomic a slight, but significant tendency was demonstrated for preferential pairing of the two normal chromosomes associated with the compensating complex. This promotes the desired segregation into one normal and one compensating karyotype. In all trisomies, however, too high a frequency of failure of chiasma formation in a critical segment of the complex was evident. This is correlated with the ease of recovery of the trisomics, but results in undesired segregational products. Interstitial chiasmata leading to the formation of branched configurations were also present, more in some trisomics than in others. These also result in undesired segregations. The behaviour at meiosis was so closely correlated with the length of the chromosome segments involved that a prediction of the most favourable combination of telocentric and translocation can be made. The telocentric should be large, the corresponding translocated segment large and the interstitial segment small. The non-translocated arm of the translocated chromosome should be large and the second translocated segment small. The combinations of translocations and telocentrics had not been selected for these criteria and did not meet the requirements for practical application.
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Rice (N Y)
March 2023
Jiangsu Key Laboratory of Crop Genomics and Molecular Breeding/Key Laboratory of Plant Functional Genomics of the Ministry of Education/Jiangsu Key Laboratory of Crop Genetics and Physiology, Agricultural College of Yangzhou University, Yangzhou, 225009, China.
Aneuploid refers to the gene dosage imbalance due to copy number alterations. Aneuploidy is generally harmful to the growth, development and reproduction of organisms according to the numerous research. However, it has rarely been reported on whether aneuploid have a relevant pattern of genome expression between the parental and its offspring generations.
View Article and Find Full Text PDFDev Cell
February 2020
Department of Neurology, University of Massachusetts Medical School, Worcester, MA 01655, USA; Department of Pediatrics, University of Massachusetts Medical School, Worcester, MA 01655, USA. Electronic address:
The ability of XIST to dosage compensate a trisomic autosome presents unique experimental opportunities and potentially transformative therapeutic prospects. However, it is currently thought that XIST requires the natural context surrounding pluripotency to initiate chromosome silencing. Here, we demonstrate that XIST RNA induced in differentiated neural cells can trigger chromosome-wide silencing of chromosome 21 in Down syndrome patient-derived cells.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
November 2018
Division of Biological Sciences, University of Missouri, Columbia, MO 65211;
Changes in dosage of part of the genome (aneuploidy) have long been known to produce much more severe phenotypic consequences than changes in the number of whole genomes (ploidy). To examine the basis of these differences, global gene expression in mature leaf tissue for all five trisomies and in diploids, triploids, and tetraploids of was studied. The trisomies displayed a greater spread of expression modulation than the ploidy series.
View Article and Find Full Text PDFSci Rep
January 2018
Department of Biochemistry and Biophysics, University of Rochester Medical Center, Rochester, New York, USA.
Candida albicans is a diploid fungus and a predominant opportunistic human pathogen. Notably, C. albicans employs reversible chromosomal aneuploidies as a means of survival in adverse environments.
View Article and Find Full Text PDFPLoS One
February 2016
Linda Crnic Institute for Down Syndrome, Department of Pediatrics, University of Colorado Denver, Mail Stop 8608, 12700 E 19th Avenue, Aurora, Colorado 80045, United States of America; Department of Biochemistry and Molecular Genetics, University of Colorado Denver, Mail Stop 8608, 12700 E 19th Avenue, Aurora, Colorado 80045, United States of America; Human Medical Genetics and Genomics, and Neuroscience Programs, University of Colorado Denver, Mail Stop 8608, 12700 E 19th Avenue, Aurora, Colorado 80045, United States of America.
Down syndrome (DS) is caused by an extra copy of human chromosome 21 (Hsa21). Although it is the most common genetic cause of intellectual disability (ID), there are, as yet, no effective pharmacotherapies. The Ts65Dn mouse model of DS is trisomic for orthologs of ∼55% of Hsa21 classical protein coding genes.
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