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Journal articles on the topic 'Paracentric inversion'

Author: Grafiati

Published: 2 June 2025

Last updated: 31 July 2025

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1

Singh, B. N., and Aparup Das. "Inversion polymorphism in Indian natural populations of Drosophila melonogaster." Genome 33, no. 3 (1990): 311–16. http://dx.doi.org/10.1139/g90-048.

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Six natural populations (three urban and three rural) of Drosophila melonogaster from India were analysed for chromosome inversions, revealing the presence of 19 different paracentric autosomal inversions. One new inversion has also been detected in a laboratory stock established from flies collected from Kerala. In total 20 different paracentric inversions in Indian D. melonogaster have been detected during the present study, and of these, 4 are common cosmopolitans; 2 are rare cosmopolitans; 7 are recurrent endemics; and 7 are unique endemics. The quantitative data clearly show that the urba

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2

Werle, Sean F., Ed Klekowski, and Douglas G. Smith. "Inversion polymorphism in a Connecticut River Axarus species (Diptera: Chironomidae): biometric effects of a triple inversion heterozygote." Canadian Journal of Zoology 82, no. 1 (2004): 118–29. http://dx.doi.org/10.1139/z03-227.

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The authors sampled three spatially isolated populations of a chironomid midge in the genus Axarus living in the Connecticut River both early and late in the larval life cycle of one generation. Larvae were scored for both length and inversion frequency using the polytene chromosomes from salivary gland cells. We found polymorphism for four paracentric inversions. Inversion C1–6 exhibits a geographic cline, increasing in frequency with increasing latitude but remaining stable over time. Also stable over time were two other paracentric inversions designated A1–5 and F13–20, which were present a

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3

Bettio, D., N. Rizzi, and D. Giardino. "Case of paracentric inversion 19p." American Journal of Medical Genetics 58, no. 4 (1995): 386. http://dx.doi.org/10.1002/ajmg.1320580424.

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4

Rigola, Maria A., Neus Baena, Vicenç Català, et al. "A 11.7-Mb Paracentric Inversion in Chromosome 1q Detected in Prenatal Diagnosis Associated with Familial Intellectual Disability." Cytogenetic and Genome Research 146, no. 2 (2015): 109–14. http://dx.doi.org/10.1159/000437127.

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Most apparent balanced chromosomal inversions are usually clinically asymptomatic; however, infertility, miscarriages, and mental retardation have been reported in inversion carriers. We present a small family with a paracentric inversion 1q42.13q43 detected in routine prenatal diagnosis. Molecular cytogenetic methods defined the size of the inversion as 11.7 Mb and excluded other unbalanced chromosomal alterations in the patients. Our findings suggest that intellectual disability is caused by dysfunction, disruption, or position effects of genes located at or near the breakpoints involved in

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5

Д.А., Юрченко,, Тарлычева, А.А., Миньженкова, М.Е., Маркова, Ж.Г., and Шилова, Н.В. "Estimation of the frequency of recombination in the inversion loop in a carrier of polymorphic paracentric inversion 8p23.1." Nauchno-prakticheskii zhurnal «Medicinskaia genetika, no. 12 (December 26, 2022): 60–63. http://dx.doi.org/10.25557/2073-7998.2022.12.60-63.

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Парацентрическая инверсия 8р23.1 является одной из самых протяженных полиморфных инверсий у человека. В результате патологической мейотической сегрегации парацентрической инверсии образуются гаметы и впоследствии зиготы с рекомбинантными хромосомами, а именно с хромосомным/геномным дисбалансом в виде инвертированной дупликации со смежной делецией (inv dup del) или с терминальной делецией (del). В исследовании впервые проведена оценка частоты рекомбинации в инверсионной петле у носителя полиморфной парацентрической инверсии 8р23.1. Установлено, что в мужском гаметогенезе при гетерозиготном носи

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6

Callen, David F. "Alternative Interpretation of Reported Paracentric Inversion." American Journal of Human Genetics 63, no. 1 (1998): 269–70. http://dx.doi.org/10.1086/301902.

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7

Schmid, M., R. Hofmann, J. Köhler, and U. Jannek. "Familial paracentric inversion in(2)(q31q36)." Human Genetics 71, no. 3 (1985): 270–72. http://dx.doi.org/10.1007/bf00284590.

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8

Bell, Judith, Robyn Dunlop, and Jennifer Bryan. "Another paracentric inversion of chromosome 18." American Journal of Medical Genetics 39, no. 2 (1991): 238. http://dx.doi.org/10.1002/ajmg.1320390230.

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9

Ruiz, Alfredo, José María Ranz, Mario Cáceres, and Carmen Segarra. "Chromosomal evolution and comparative gene mapping in the Drosophila repleta species group." Brazilian Journal of Genetics 20, no. 4 (1997): 553–65. http://dx.doi.org/10.1590/s0100-84551997000400003.

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A review of our recent work on the cromosomal evolution of the Drosophila repleta species group is presented. Most studies have focused on the buzzatii species complex, a monophyletic set of 12 species which inhabit the deserts of South America and the West Indies. A statistical analysis of the length and breakpoint distribution of the 86 paracentric inversions observed in this complex has shown that inversion length is a selected trait. Rare inversions are usually small while evolutionary successful inversions, fixed and polymorphic, are predominantly of medium size. There is also a negative

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10

Navas-Castillo, J., J. Cabrero, and J. P. M. Camacho. "Paracentric inversion in the grasshopper Oedipoda charpentieri." Heredity 59, no. 3 (1987): 441–44. http://dx.doi.org/10.1038/hdy.1987.153.

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11

Gaur, Sumit, and V. Shukla. "Paracentric inversion of chromosome 12 in myelodysplasia." American Journal of Hematology 78, no. 4 (2005): 318–19. http://dx.doi.org/10.1002/ajh.20325.

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12

Dar, Hanna, Joseph Tal, Hanna Bar-el, et al. "Paracentric inversion of Xq and ovarian dysfunction." American Journal of Medical Genetics 29, no. 1 (1988): 167–70. http://dx.doi.org/10.1002/ajmg.1320290122.

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13

Hammer, M. F., S. Bliss, and L. M. Silver. "Genetic exchange across a paracentric inversion of the mouse t complex." Genetics 128, no. 4 (1991): 799–812. http://dx.doi.org/10.1093/genetics/128.4.799.

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Abstract Mouse t haplotypes are distinguished from wild-type forms of chromosome 17 by four nonoverlapping paracentric inversions which span a genetic distance of 20 cM. These inversion polymorphisms are responsible for a 100-200-fold suppression of recombination which maintains the integrity of complete t haplotypes and has led to their divergence from the wild-type chromosomes of four species of house mice within which t haplotypes reside. As evidence for the long period of recombinational isolation, alleles that distinguish all t haplotypes from all wild-type chromosomes have been establish

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14

Das, Aparup, and B. N. Singh. "Genetic differentiation and inversion clines in Indian natural populations of Drosophila melanogaster." Genome 34, no. 4 (1991): 618–25. http://dx.doi.org/10.1139/g91-094.

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To study the genetic differentiation and inversion clines in Indian natural populations of Drosophila melanogaster, 14 natural populations (6 from the north and 8 from the south) were screened for chromosome inversions. The chromosomal analysis revealed the presence of 23 paracentric inversions, which include 4 common cosmopolitan, 4 rare cosmopolitan, 2 recurrent endemic, and 13 unique endemic (new inversions detected for the first time) inversions. The difference in karyotype frequencies between populations from the north and south were highly significant and the level of inversion heterozyg

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15

Poopittayasataporn, Anan, and Visut Baimai. "Polytene chromosome relationships of five species of the Anopheles dirus complex in Thailand." Genome 38, no. 3 (1995): 426–34. http://dx.doi.org/10.1139/g95-056.

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Photographic maps and rearrangements of each salivary gland polytene chromosome arm of Anopheles nemophilous (species F) and of An. dirus species A, B, C, and D of the Dirus group from natural populations in Thailand are presented. Structural conformation of heterokaryotypes and comparison of chromosome banding sequences reveal 10 paracentric inversions. The data on fixed inversion of 3Rb and inversion polymorphism of the X chromosome shared by these species were used to construct a phylogeny of the five members of the An. dirus complex, thereby outlining their patterns of speciation through c

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16

Herr, H. M., S. J. Horton, and C. I. Scott. "De novo paracentric inversion in an X chromosome." Journal of Medical Genetics 22, no. 2 (1985): 140–42. http://dx.doi.org/10.1136/jmg.22.2.140.

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17

Pellegrini, Sandra, Maria Ribeiro, Evelyn Kahn, et al. "Familial Study of Paracentric Inversion in Chromosome 3p." British Journal of Medicine and Medical Research 3, no. 3 (2016): 760–70. http://dx.doi.org/10.9734/bjmmr/2013/2170.

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18

Pérez, C., E. Lloveras, L. Zamora, C. Melero, E. Pérez, and A. Plaja. "Prenatal detection of a paracentric inversion 16(q11.2q13)." Annales de Génétique 45, no. 3 (2002): 141–42. http://dx.doi.org/10.1016/s0003-3995(02)01125-5.

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19

Uehara, Shigeki, Shingo Tanigawara, Yoichi Takeyama, Toshifumi Takabayashi, Kunihiro Okamura, and Akira Yajima. "Paracentric inversion of chromosome 14: A case report." Japanese journal of human genetics 39, no. 3 (1994): 353–56. http://dx.doi.org/10.1007/bf01874054.

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20

Madan, K., M. H. E. C. Pieters, L. P. Kuyt, et al. "Paracentric inversion inv(11) (q21q23) in the Netherlands." Human Genetics 85, no. 1 (1990): 15–20. http://dx.doi.org/10.1007/bf00276319.

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21

Inayama, Yasuhiro, Hiroshi Yoneda, Kentaro Fukushima, Jun Sakai, Hiroyuki Asaba, and Toshiaki Sakai. "Paracentric inversion of chromosome 9 with schizoaffective disorder." Clinical Genetics 51, no. 1 (2008): 69–70. http://dx.doi.org/10.1111/j.1399-0004.1997.tb02419.x.

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22

Warburton, Dorothy, and Sivya Twersky. "Risk of phenotypic abnormalities in paracentric inversion carriers." American Journal of Medical Genetics 69, no. 2 (1997): 219. http://dx.doi.org/10.1002/(sici)1096-8628(19970317)69:2<219::aid-ajmg20>3.0.co;2-n.

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23

Phelan, Mary C., Richard J. Schroer, and Ernest F. Krug. "Paracentric inversion of chromosome 19 in three generations." American Journal of Medical Genetics 34, no. 4 (1989): 525–27. http://dx.doi.org/10.1002/ajmg.1320340414.

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24

Siegel, Selma F., Mamdouha Ahdab-Barmada, Silva Arslanian, and Thomas P. Foley. "Ectopic posterior pituitary tissue and paracentric inversion of the short arm of chromosome 1 in twins." European Journal of Endocrinology 133, no. 1 (1995): 87–92. http://dx.doi.org/10.1530/eje.0.1330087.

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Siegel SF, Ahdab-Barmada M, Arslanian S, Foley Jr TP. Ectopic posterior pituitary tissue and paracentric inversion of the short arm of chromosome 1 in twins. Eur J Endocrinol 1995;133:87–92. ISSN 0804–4643 Twin boys with hypopituitarism, hypoplasia of the anterior pituitary gland, ectopic posterior pituitary tissue and paracentric inversion of the short arm of chromosome 1 are described. The smooth appearance at the base of the median eminence and the absence of a pituitary stalk at autopsy in these boys implies that the hypopituitarism resulted from a developmental aberration. It remains to b

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25

Cáceres, Mario, Antonio Barbadilla, and Alfredo Ruiz. "Recombination Rate Predicts Inversion Size in Diptera." Genetics 153, no. 1 (1999): 251–59. http://dx.doi.org/10.1093/genetics/153.1.251.

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Abstract Most species of the Drosophila genus and other Diptera are polymorphic for paracentric inversions. A common observation is that successful inversions are of intermediate size. We test here the hypothesis that the selected property is the recombination length of inversions, not their physical length. If so, physical length of successful inversions should be negatively correlated with recombination rate across species. This prediction was tested by a comprehensive statistical analysis of inversion size and recombination map length in 12 Diptera species for which appropriate data are ava

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26

Kasai, Ryozo, Kouji Narahara, Kiyoshi Kikkawa, et al. "Reproductive risk of paracentric inversion carriers: Report of two unrelated cases with paracentric inversion of the long ARM of chromosome 3." Japanese journal of human genetics 30, no. 2 (1985): 57–67. http://dx.doi.org/10.1007/bf01873578.

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27

Pickering, R. A. "Comparison of crossover frequencies in barley (Hordeum vulgare) and H. vulgare × H. bulbosum hybrids using a paracentric inversion." Genome 34, no. 4 (1991): 666–73. http://dx.doi.org/10.1139/g91-102.

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Crosses between different parental ploidy combinations of barley (Hordeum vulgare L.) and H. bulbosum L. have been carried out principally to obtain hybrids with high allosyndetic chromosome pairing. Fertility has been observed in tetraploid and triploid hybrids, but there has been little evidence of gene introgression from H. bulbosum into H. vulgare in their progeny. To investigate whether crossing-over takes place between homoeologous chromosomes of H. vulgare and H. bulbosum, diploid hybrids were obtained from crosses between a barley mutant (wst3) homozygous for a paracentric inversion on

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28

Maguire, Marjorie P. "Evidence on the nature and complexity of the mechanism of chiasma maintenance in maize." Genetical Research 45, no. 1 (1985): 37–49. http://dx.doi.org/10.1017/s0016672300021947.

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SummaryInferences on the mechanism of chiasma maintenance can be drawn from study of the distribution and frequency of chiasma-like associations between bridges and fragments and between normal chromatids and fragments in meiotic material heterozygous for paracentric inversions. These bridges and fragments are the result of crossing over within the inverted region so that differing predictions for the associations are generated by the various models for chiasma maintenance mechanism. Results of such a study in material heterozygous for a large paracentric inversion in the long arm of chromosom

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29

María, José, Carmen Segarra, and Alfredo Ruiz. "Chromosomal Homology and Molecular Organization of Muller's Elements D and E in the Drosophila repleta Species Group." Genetics 145, no. 2 (1997): 281–95. http://dx.doi.org/10.1093/genetics/145.2.281.

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Thirty-three DNA clones containing protein-coding genes have been used for in situ hybridization to the polytene chromosomes of two Drosophila repleta group species, D. repleta and D. buzzatii. Twenty-six clones gave positive results allowing the precise localization of 26 genes and the tentative identification of another nine. The results were fully consistent with the currently accepted chromosomal homologies and in no case was evidence for reciprocal translocations or pericentric inversions found. Most of the genes mapped to chromosomes 2 and 4 that are homologous, respectively, to chromoso

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30

Bateman, B. G., R. Neu, W. C. Nunley, and T. E. Kelly. "Pregnancy wastage associated with paracentric inversion of chromosome 13." Journal of Medical Genetics 23, no. 4 (1986): 370. http://dx.doi.org/10.1136/jmg.23.4.370.

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31

Bahl, J. R., and B. R. Tyagi. "A case of paracentric inversion in Papaver dubium L." CYTOLOGIA 53, no. 4 (1988): 777–82. http://dx.doi.org/10.1508/cytologia.53.777.

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32

Vialard, François, Audoin Delanete, Patrice Clement, Brigitte Simon-Bouy, François Xavier Aubriot, and Jacqueline Selva. "Sperm chromosome analysis in two cases of paracentric inversion." Fertility and Sterility 87, no. 2 (2007): 418.e1–418.e5. http://dx.doi.org/10.1016/j.fertnstert.2006.05.087.

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33

Kuvangkadilok, Chaliow, Suwannee Phayuhasena, and Visut Baimai. "Population cytogenetic studies on Simulium feuerborni Edwards (Diptera: Simuliidae) from northern Thailand." Genome 42, no. 1 (1999): 80–86. http://dx.doi.org/10.1139/g98-106.

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A standard photographic map of Simulium feuerborni (Diptera: Simuliidae) was constructed from larval salivary gland polytene chromosomes and is described herein. Analysis of polytene chromosomes was made from wild larvae collected from the four populations at Doi Inthanon National Park, Chiang Mai Province, northern Thailand. Simulium feuerborni has three pairs of chromosomes (2n = 6) which are arranged from the longest to the shortest. Chromosome I is metacentric while chromosomes II and III are submetacentric. A total of six simple paracentric inversions have been detected in these natural p

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34

Madan, K., and A. W. M. Nieuwint. "Reproductive risks for paracentric inversion heterozygotes: Inversion or insertion? That is the question." American Journal of Medical Genetics 107, no. 4 (2002): 340–43. http://dx.doi.org/10.1002/ajmg.10173.

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35

Stocker, Ann Jacob, Brad Foley, and Ary Hoffmann. "Inversion frequencies in Drosophila serrata along an eastern Australian transect." Genome 47, no. 6 (2004): 1144–53. http://dx.doi.org/10.1139/g04-078.

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Clinal patterns over broad geographic regions provide a way of identifying characteristics of species under selection and are increasingly being used in quantitative trait locus mapping of adaptive genetic variation in Drosophila. However, interpretations of clinal patterns can be complicated by inversions that also vary clinally and reduce recombination in some parts of the genome. Drosophila serrata (Malloch) is an Australian endemic species being used to investigate the genetic basis of geographic variation in climatic adaptation and mate recognition. Here we describe inversions in D. serra

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36

Devos, K. M., S. Chao, Q. Y. Li, M. C. Simonetti, and M. D. Gale. "Relationship between chromosome 9 of maize and wheat homeologous group 7 chromosomes." Genetics 138, no. 4 (1994): 1287–92. http://dx.doi.org/10.1093/genetics/138.4.1287.

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Abstract Comparison of the genetic map of maize chromosome 9 with maps of wheat chromosomes has revealed a high degree of colinearity between maize chromosome 9 and the group 4 and 7 chromosomes of wheat. The order of DNA markers on the short arm and a proximal region of the long arm of the genetic map of maize chromosome 9 is highly conserved with the marker order on the short arm and proximal region of the long arm of the genetic map of the wheat homeologous group 7 chromosomes. A major part of the long arm of the genetic map of maize chromosome 9 is homeologous with a short segment in the p

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37

Doganlar, Sami, Anne Frary, Marie-Christine Daunay, Richard N. Lester, and Steven D. Tanksley. "A Comparative Genetic Linkage Map of Eggplant (Solanum melongena) and Its Implications for Genome Evolution in the Solanaceae." Genetics 161, no. 4 (2002): 1697–711. http://dx.doi.org/10.1093/genetics/161.4.1697.

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Abstract A molecular genetic linkage map based on tomato cDNA, genomic DNA, and EST markers was constructed for eggplant, Solanum melongena. The map consists of 12 linkage groups, spans 1480 cM, and contains 233 markers. Comparison of the eggplant and tomato maps revealed conservation of large tracts of colinear markers, a common feature of genome evolution in the Solanaceae and other plant families. Overall, eggplant and tomato were differentiated by 28 rearrangements, which could be explained by 23 paracentric inversions and five translocations during evolution from the species' last common

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38

García, Beatriz A., Adalgisa Caccone, Kostas D. Mathiopoulos, and Jeffrey R. Powell. "Inversion Monophyly in African Anopheline Malaria Vectors." Genetics 143, no. 3 (1996): 1313–20. http://dx.doi.org/10.1093/genetics/143.3.1313.

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Abstract The African Anopheles gambzae complex of six sibling species has many polymorphic and fixed paracentric inversions detectable in polytene chromosomes. These have been used to infer phylogenetic relationships as classically done with Drosophila. Two species, A. gambiae and A. merus, were thought to be sister taxa based on a shared X inversion designated Xag. Recent DNA data have conflicted with this phylogenetic inference as they have supported a sister taxa relationship of A. gambiaeand A. arabiensis. A possible explanation is that the Xag is not monophyletic. Here we present data fro

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39

Watt, J. L., K. Ward, D. A. Couzin, G. S. Stephen, and A. Hill. "A paracentric inversion of 7q illustrating a possible interchromosomal effect." Journal of Medical Genetics 23, no. 4 (1986): 341–44. http://dx.doi.org/10.1136/jmg.23.4.341.

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40

Garcia-Guixé, Elena, Carles Giménez I Sevilla, Estefanía Toro Toro, et al. "Higher than expected reproductive risk for autosomal paracentric inversion carriers." Reproductive BioMedicine Online 36 (March 2018): e33-e34. http://dx.doi.org/10.1016/j.rbmo.2017.10.081.

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41

D'Alessandro, Elvira, Corinna De Matteis, Maria Luisa Lo Re, et al. "Paracentric inversion of chromosome 15(q15q24): description of three families." Human Genetics 87, no. 2 (1991): 123–24. http://dx.doi.org/10.1007/bf00204165.

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42

Liu, Qing, Luke B. Hesson, Andrea C. Nunez, et al. "A cryptic paracentric inversion ofMSH2exons 2–6 causes Lynch syndrome." Carcinogenesis 37, no. 1 (2015): 10–17. http://dx.doi.org/10.1093/carcin/bgv154.

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43

Díez, M., and J. L. Santos. "Synapsis in a paracentric inversion heterozygote of Chorthippus jacobsi (grasshopper)." Heredity 70, no. 3 (1993): 231–36. http://dx.doi.org/10.1038/hdy.1993.34.

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44

Grass, Frank S., James C. Parke, and John C. Hisley. "Antenatal diagnosis of ade novo paracentric inversion of chromosome 11." Prenatal Diagnosis 7, no. 1 (1987): 1–5. http://dx.doi.org/10.1002/pd.1970070102.

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45

Donti, Emilio, Antonella Rosetti, Ida Carloni, and Giovanna Venti Donti. "A new case of familial paracentric inversion of chromosome 2." Human Genetics 75, no. 2 (1987): 195. http://dx.doi.org/10.1007/bf00591087.

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46

Green, C. A., B. A. Harrison, T. Klein, and V. Baimai. "Cladistic analysis of polytene chromosome rearrangements in anopheline mosquitoes, subgenus Cellia, series Neocellia." Canadian Journal of Genetics and Cytology 27, no. 2 (1985): 123–33. http://dx.doi.org/10.1139/g85-020.

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New data on rearrangements of ovarian polytene chromosomes from mosquitoes are presented for the following species in the series Neocellia of Anopheles (Cellia): annularis, philippinensis, nivipes, splendidus, jamesii, and ramsayi. Rearrangement has involved fixation of alternatives for paracentric inversions. Two fixed inversion differences allow for the first time the direct identification of wild-caught females of philippinensis and nivipes. There is a suggestion that the latter nominal species may include two genetic species. These data and those published for close relatives are drawn tog

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47

Karamysheva, Tatyana V., Tatyana A. Gayner, Eugeny A. Elisaphenko, et al. "The Precise Breakpoint Mapping in Paracentric Inversion 10q22.2q23.3 by Comprehensive Cytogenomic Analysis, Multicolor Banding, and Single-Copy Chromosome Sequencing." Biomedicines 10, no. 12 (2022): 3255. http://dx.doi.org/10.3390/biomedicines10123255.

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Detection and precise genomic mapping of balanced chromosomal abnormalities in patients with impaired fertility or a clinical phenotype represent a challenge for current cytogenomics owing to difficulties with precise breakpoint localization in the regions enriched for DNA repeats and high genomic variation in such regions. Here, we present a comprehensive cytogenomic approach to breakpoint mapping in a rare paracentric inversion on 10q (in a patient with oligoasthenoteratozoospermia and necrozoospermia) that does not affect other phenotype traits. Multicolor banding, chromosomal microarray an

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48

Lall, Meena, Pushpa Saviour, Ratna Puri, and Ishwar Verma. "A familial deletion 4q syndrome: An outcome of a paracentric inversion." Indian Journal of Human Genetics 18, no. 2 (2012): 238. http://dx.doi.org/10.4103/0971-6866.100780.

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49

Laufs, Patrick, Daphne Autran, and Jan Traas. "A chromosomal paracentric inversion associated with T-DNA integration in Arabidopsis." Plant Journal 18, no. 2 (1999): 131–39. http://dx.doi.org/10.1046/j.1365-313x.1999.00436.x.

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50

Cook, S. A., E. C. Akeson, C. Calvano, et al. "Mouse paracentric inversion In(3)55Rk mutates the urate oxidase gene." Cytogenetic and Genome Research 93, no. 1-2 (2001): 77–82. http://dx.doi.org/10.1159/000056953.

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