Maternal imprinting effect on B chromosome transmission in rye

In this study, we describe a strategy to determine the presence of B chromosomes in the living grasshopper Abracris flavolineata by FISH using U2 snDNA as a probe in interphase hemolymph nuclei. In individuals without B chromosomes, (0B) 2 dot signals were noticed, corresponding to A complement U2 snDNA clusters. In +1B and +2B individuals, 4 or 8 additional signals were noticed, respectively. In all cases, the absence or presence of 1 or 2 B chromosomes correlated in hemolymph and in somatic or germline tissues, validating the efficiency of the marker. Our data suggest that the B chromosome of A. flavolineata is present in all somatic tissues. B-carrying individuals showed the same number of B chromosomes in germ and somatic cells, suggesting that the B is mitotically stable. The marker was used to compare B chromosome frequency in the analyzed population with a sample collected previously, in order to test for B frequency changes and differences of B chromosome prevalence among sexes, but no statistically significant differences were noticed. The identification of living animals harboring B chromosomes will be very useful in future studies of B chromosome transmission, as well as in functional studies involving RNA analysis, thus contributing to the understanding of evolutionary history and the possible role of the B chromosome in A. flavolineata.

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Rye B chromosome transmission depends on the B, the carrier of the B and the mother of the carrier

Chromosomes Today ◽

10.1007/978-94-011-1510-0_30 ◽

1993 ◽

pp. 391-399 ◽

Cited By ~ 5

Author(s):

M. J. Puertas ◽

M. M. Jiménez ◽

F. Romera

Keyword(s):

B Chromosome ◽

Chromosome Transmission

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Nonrandom Segregation of the Mouse Univalent X Chromosome: Evidence of Spindle-Mediated Meiotic Drive

Genetics ◽

10.1093/genetics/156.2.775 ◽

2000 ◽

Vol 156 (2) ◽

pp. 775-783 ◽

Cited By ~ 1

Author(s):

Renée LeMaire-Adkins ◽

Patricia A Hunt

Keyword(s):

X Chromosome ◽

Chromosome Abnormality ◽

Three Dimensional ◽

Fundamental Principle ◽

Mendelian Inheritance ◽

Segregation Behavior ◽

Chromosome Transmission ◽

Distortion Effect ◽

Random Segregation ◽

Transmission Distortion

Abstract A fundamental principle of Mendelian inheritance is random segregation of alleles to progeny; however, examples of distorted transmission either of specific alleles or of whole chromosomes have been described in a variety of species. In humans and mice, a distortion in chromosome transmission is often associated with a chromosome abnormality. One such example is the fertile XO female mouse. A transmission distortion effect that results in an excess of XX over XO daughters among the progeny of XO females has been recognized for nearly four decades. Utilizing contemporary methodology that combines immunofluorescence, FISH, and three-dimensional confocal microscopy, we have readdressed the meiotic segregation behavior of the single X chromosome in oocytes from XO females produced on two different inbred backgrounds. Our studies demonstrate that segregation of the univalent X chromosome at the first meiotic division is nonrandom, with preferential retention of the X chromosome in the oocyte in ∼60% of cells. We propose that this deviation from Mendelian expectations is facilitated by a spindle-mediated mechanism. This mechanism, which appears to be a general feature of the female meiotic process, has implications for the frequency of nondisjunction in our species.

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Satellite DNA probes of Alstroemeria longistaminea (Alstroemeriaceae) paint the heterochromatin and the B chromosome, reveal a G-like banding pattern, and point to a strong structural karyotype conservation

PROTOPLASMA ◽

10.1007/s00709-021-01681-7 ◽

2021 ◽

Author(s):

Tiago Ribeiro ◽

Magdalena Vaio ◽

Leonardo P. Félix ◽

Marcelo Guerra

Keyword(s):

Banding Pattern ◽

Satellite Dna ◽

B Chromosome ◽

Dna Probes

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ALTERED FIDELITY OF MITOTIC CHROMOSOME TRANSMISSION IN CELL CYCLE MUTANTS OF S. CEREVISIAE

Genetics ◽

10.1093/genetics/110.3.381 ◽

1985 ◽

Vol 110 (3) ◽

pp. 381-395

Author(s):

Leland H Hartwell ◽

David Smith

Keyword(s):

Cell Cycle ◽

Gene Product ◽

Mitotic Chromosome ◽

Mitotic Recombination ◽

Chromosome Loss ◽

Temperature Sensitive ◽

Repair Pathway ◽

Dna Metabolism ◽

Temperature Sensitive Mutants ◽

Chromosome Transmission

ABSTRACT Thirteen of 14 temperature-sensitive mutants deficient in successive steps of mitotic chromosome transmission (cdc2, 4, 5, 6, 7, 8, 9, 13, 14, 15, 16, 17 and 20) from spindle pole body separation to a late stage of nuclear division exhibited a dramatic increase in the frequency of chromosome loss and/or mitotic recombination when they were grown at their maximum permissive temperatures. The increase in chromosome loss and/or recombination is likely to be due to the deficiency of functional gene product rather than to an aberrant function of the mutant gene product since the mutant alleles are, with one exception, recessive to the wild-type allele for this phenotype. The generality of this result suggests that a delay in almost any stage of chromosome replication or segregation leads to a decrease in the fidelity of mitotic chromosome transmission. In contrast, temperature-sensitive mutants defective in the control step of the cell cycle (cdc28), in cytokinesis (cdc3) or in protein synthesis (ils1) did not exhibit increased recombination or chromosome loss.—Based upon previous results with mutants and DNA-damaging agents in a variety of organisms, we suggest that the induction of mitotic recombination in certain mutants is due to the action of a repair pathway upon nicks or gaps left in the DNA. This interpretation is supported by the fact that the induced recombination is dependent upon the RAD52 gene product, an essential component in the recombinogenic DNA repair pathway. Gene products whose deficiency leads to induced recombination are, therefore, strong candidates for proteins that function in DNA metabolism. Among the mutants that induce recombination are those known to be defective in some aspect of DNA replication (cdc2, 6, 8, 9) as well as some mutants defective in the G2 (cdc13 and 17) and M (cdc5 and 14) phases of the mitotic cycle. We suggest that special aspects of DNA metabolism may be occurring in G2 and M in order to prepare the chromosomes for proper segregation.

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Repetitive DNA landscape in essential A and supernumerary B chromosomes of Festuca pratensis Huds

Scientific Reports ◽

10.1038/s41598-019-56383-1 ◽

2019 ◽

Vol 9 (1) ◽

Author(s):

Rahman Ebrahimzadegan ◽

Andreas Houben ◽

Ghader Mirzaghaderi

Keyword(s):

Repetitive Sequences ◽

Nuclear Genome ◽

B Chromosome ◽

B Chromosomes ◽

Festuca Pratensis ◽

Ltr Retrotransposons ◽

Chromosome Identification ◽

Satellite Repeats ◽

Low Pass ◽

Illumina Sequence

AbstractHere, we characterized the basic properties of repetitive sequences in essential A and supernumerary B chromosomes of Festuca pratensis Huds. This was performed by comparative analysis of low-pass Illumina sequence reads of B chromosome lacking (−B) and B chromosome containing (+B) individuals of F. pratensis. 61% of the nuclear genome is composed of repetitive sequences. 43.1% of the genome are transposons of which DNA transposons and retrotransposons made up 2.3% and 40.8%, respectively. LTR retrotransposons are the most abundant mobile elements and contribute to 40.7% of the genome and divided into Ty3-gypsy and Ty1-copia super families with 32.97% and 7.78% of the genome, respectively. Eighteen different satellite repeats were identified making up 3.9% of the genome. Five satellite repeats were used as cytological markers for chromosome identification and genome analysis in the genus Festuca. Four satellite repeats were identified on B chromosomes among which Fp-Sat48 and Fp-Sat253 were specific to the B chromosome of F. pratensis.

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