PMID- 29114353 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20200930 IS - 1993-0771 (Print) IS - 1993-078X (Electronic) IS - 1993-0771 (Linking) VI - 11 IP - 114 DP - 2017 TI - A chromosomal analysis of Nepa cinerea Linnaeus, 1758 and Ranatra linearis (Linnaeus, 1758) (Heteroptera, Nepidae). PG - 641-657 LID - 10.3897/CompCytogen.v11i4.14928 [doi] AB - An account is given of the karyotypes and male meiosis of the Water Scorpion Nepa cinerea Linnaeus, 1758 and the Water Stick Insect Ranatra linearis (Linnaeus, 1758) (Heteroptera, Nepomorpha, Nepidae). A number of different approaches and techniques were tried: the employment of both male and female gonads and mid-guts as the sources of chromosomes, squash and air-drying methods for chromosome preparations, C-banding and fluorescence in situ hybridization (FISH) for chromosome study. We found that N. cinerea had a karyotype comprising 14 pairs of autosomes and a multiple sex chromosome system, which is X(1)X(2)X(3)X(4)Y (male symbol) / X(1)X(1)X(2)X(2)X(3)X(3)X(4)X(4) (female symbol), whereas R. linearis had a karyotype comprising 19 pairs of autosomes and a multiple sex chromosome system X(1)X(2)X(3)X(4)Y (male symbol) / X(1)X(1)X(2)X(2)X(3)X(3)X(4)X(4) (female symbol). In both N. cinerea and R. linearis, the autosomes formed chiasmate bivalents in spermatogenesis, and the sex chromosome univalents divided during the first meiotic division and segregated during the second one suggesting thus a post-reductional type of behaviour. These results confirm and amplify those of Steopoe (1925, 1927, 1931, 1932) but are inconsistent with those of other researchers. C-banding appeared helpful in pairing up the autosomes for karyotype assembly; however in R. linearis the chromosomes were much more uniform in size and general appearance than in N. cinerea. FISH for 18S ribosomal DNA (major rDNA) revealed hybridization signals on two of the five sex chromosomes in N. cinerea. In R. linearis, rDNA location was less obvious than in N. cinerea; however it is suggested to be similar. We have detected the presence of the canonical "insect" (TTAGG) (n) telomeric repeat in chromosomes of these species. This is the first application of C-banding and FISH in the family Nepidae. FAU - Angus, Robert B AU - Angus RB AD - Department of Life Sciences (Insects), The Natural History Museum, Cromwell Road, London SW7 5BD, UK. FAU - Jeangirard, Constance AU - Jeangirard C AD - School of Biological Sciences, Royal Holloway University of London, Egham, Surrey TW20 0EX, UK. FAU - Stoianova, Desislava AU - Stoianova D AD - Institute of Biodiversity and Ecosystem Research, Bulgarian Academy of Sciences, 1 Tsar Osvoboditel, Sofia 1000, Bulgaria. FAU - Grozeva, Snejana AU - Grozeva S AD - Institute of Biodiversity and Ecosystem Research, Bulgarian Academy of Sciences, 1 Tsar Osvoboditel, Sofia 1000, Bulgaria. FAU - Kuznetsova, Valentina G AU - Kuznetsova VG AD - Zoological Institute, Russian Academy of Sciences, Universitetskaya nab. 1, St. Petersburg 199034, Russia. LA - eng PT - Journal Article DEP - 20170914 PL - Bulgaria TA - Comp Cytogenet JT - Comparative cytogenetics JID - 101503807 PMC - PMC5672273 OTO - NOTNLM OT - (TTAGG)n OT - 18S rDNA OT - C-banding OT - FISH OT - Heteroptera OT - Karyotype OT - Nepa cinerea OT - Nepomorpha OT - Ranatra linearis OT - male meiosis EDAT- 2017/11/09 06:00 MHDA- 2017/11/09 06:01 PMCR- 2017/09/14 CRDT- 2017/11/09 06:00 PHST- 2017/06/07 00:00 [received] PHST- 2017/08/13 00:00 [accepted] PHST- 2017/11/09 06:00 [entrez] PHST- 2017/11/09 06:00 [pubmed] PHST- 2017/11/09 06:01 [medline] PHST- 2017/09/14 00:00 [pmc-release] AID - 10.3897/CompCytogen.v11i4.14928 [doi] PST - epublish SO - Comp Cytogenet. 2017 Sep 14;11(114):641-657. doi: 10.3897/CompCytogen.v11i4.14928. eCollection 2017.