Non-reciprocal gonadal dysgenesis in hybrids of the chironomid midge Chironomus thummi II. Gonadal-dysgenesis inducing chromosomes

Females of Chironomus thummi thummi (stock H1) were backcrossed with hybrid males of the cross Ch. thummi thummi (H1) x Ch. thummi piger (E) in order to test which of the four piger chromosomes determine the temperature sensitive non-reciprocal gonadal dysgenesis originally observed in the thummi x piger hybrids. In the backcross rudimentary gonads as well as normal gonads were found irrespective of the chromosome constitution of the individuals. The highest frequency of abnormal gonads (63%) occurred in backcross larvae which received piger chromosomes I and III. Statistical evaluation of the data showed that piger chromosome I is able to induce 44% dysgenic gonads. The gonadal-dysgenesis inducing ability of piger chromosome III is only recognizable if also piger chromosome I is present in the genome. The piger chromosomes II and IV do not have a statistically significant influence on the frequency of abnormal gonads.Arguments are presented for the assumption that the factors determining rudimentary development of the gonads are located distally to those pericentric chromosome regions of the piger chromosomes I and III that in polytene chromosomes show differences in the size of bands in comparison with the homologous thummi regions. The question is discussed whether the rudimentary development of the gonads is caused by gene pairs with an epistatic form of interaction or by the activity of transposable elements.     

Different hybrid effects in reciprocal crosses betweenChironomus thummi thummi andCh. th. piger including spontaneous chromsome aberrations and sterility

Hybrids from reciprocal erosses between twoChironomus thummi thummi andCh. th. piger laboratory stocks show four abnormalities in comparison to the parental stocks. One cross direction (Ch. th. thummi x Ch. th. piger ) is characterized by chromosome aberrations, reduced hatchability and malformations, whereas in reciprocal hybrids both sexes are sterile. Sterility is the consequence of rudimentary or non developed gonads.InCh. th. thummi x Ch. th. piger crosses chromosome aberrations were analysed in salivary gland nuclei. These aberrations are all somatic in origin, and they are induced during the first 40 h of embryonic development, prior to the onset of polytenization. The chromosomes of both subspecies are equally affected. In all four chromosomes breaks occur preferentially at specific regions. Reduced hatchability and malformations are presumably caused by chromosome mutations because within egg-masses a correlation exists between the rate of salivary gland chromosome aberrations and the rates of hatchability and malformations.     

Cloning and analysis of ribosomal DNA of Chironomus thummi piger and chironomus thummi thummi

The ribosomal DNAs from Ch. thummi piger and Ch. th. thummi were cloned and analysed by a variety of restriction endonucleases. Comparison of rDNA clones from the two subspecies revealed a considerable length difference: the length of the analysed rDNA cistrons is approximately 9.0 kb for Ch. th. piger and approximately 14.5 kb for Ch. th. thummi. The nearly 5 kb additional DNA in Ch. th. thummi is clearly located within the non-transcribed spacer region, and consists of AT-rich, reptitive DNA elements. These elements with a basic repeat length of approximately 120 bp, are arranged tandemly in stretches of up to about 50 identical copies, which are characterized by a cleavage site for ClaI restriction endonuclease. They are found only in the Ch. th. thummi rDNA clones and not in the Ch. th. piger clones. Southern hybridizations between cloned ribosomal DNA and centromeric highly repetitive DNA have shown that the ribosomal repetitive Cla-elements are closely related to a highly repetitive DNA sequence family, which is present in various chromosomal sites particularly the centromeres. Sequence analysis has revealed more than 90% homology between the ribosomal Cla-elements and the centromeric Cla-elements. — Since it is clear from cytological investigations that Ch. th. piger with the small rDNA repeating unit is the phylogenetically older subspecies, we postulate a transposition of Cla-elements into the nucleolar DNA during the evolution of Ch. th. thummi.     

Identification of a polytene chromosome band containing a male sex determiner of Chironomus thummi thummi

Hybrid males of Chironomus thummi piger x Ch. th. thummi crosses were backcrossed with females of both parental stocks. Fourth-instar larvae of these backcrosses showed sex specific differences in the pairing behavior of region D₃d-g in chromosome arm F of salivary gland chromosome III. — Analysis of the banding pattern of region D₃d-g after RB and quinacrine staining demonstrated that in piger x thummi hybrid males a single selectively stained band occurs within this region in the heterozygous condition at map position D₃e₁. This band could only be found in the thummi chromosome partner, it is heterochromatic and contains AT-rich DNA. In female hybrid larvae, however, such a selectively stained band is present in neither the thummi nor the piger chromosome region D₃d-g. From these results it is concluded that the selectively stained band D₃e₁ represents the male sex determiner of our Ch. th. thummi stock and that the male is the heterogametic sex.     

An AT-rich DNA component in the genomes of Chironomus thummi thummi and Chironomus thummi piger

A DNA fraction has been isolated from total Chironomus thummi thummi DNA which is discernible from the bulk Ch. th. thummi DNA by a lower thermal stability. In situ hybridizations with polytene salivary gland chromosomes of Ch. th. thummi and Ch. th. piger made localization of this DNA fraction possible. Hybridizations with bands which contain different amounts of DNA in the two subspecies indicate that the isolated DNA fraction mostly consists of those sequences which represent the genetical difference between thummi and piger.This paper is dedicated to Professor Dr. H. Bauer on the occasion of his 75th birthday     

Non-reciprocal gonadal dysgenesis in hybrids of the chironomid midge Chironomus thummi

In male hybrids of the cross Chironomus thummi thummi (stock Hl) x Ch. th. piger (stock E) , but not the reciprocal cross, rudimentary testes develop at a growth temperature of 21 ° C. Within the dysgenic testes of these hybrids a number of abnormalities are observed which are restricted to the germ line. Approximately 60% of the hybrid males show allocyclic chromosome behaviour in spermatogonia and spermatocyte I nuclei. Within these nuclei two groups of four chromosomes are formed which differ from one another in their state of condensation. Each chromosome group consists of three long and one short chromosome. In cases where allocycly is very pronounced, the chromosomes of both groups disintegrate into numerous unequally sized fragments at meiotic prometaphase I, and gametes are not produced. In individuals, in which the allocycly is less pronounced or absent the nuclear divisions appear to be normal but chromosome and chromatid aberrations are frequent, and the number of viable sperm is reduced. In these males, the chiasma frequency is also decreased more than 12-fold in comparison with the reciprocal, unaffected piger x thummi hybrids.     

Localization of a male sex determining chromosome region in Chironomus thummi piger

Chironomus th. thummi x Ch. th. piger hybrid males were backcrossed with Ch. th. thummi females. The salivary gland chromosomes of both sexes of the backcross progeny were then studied in respect to their pairing behavior. Region D₃d-g of chromosome III showed sex specific pairing. It is concluded that within this D₃d-g region a male sex determiner of Ch. th. piger is located and that the male is the heterogametic sex.     

Analysis of a repetitive DNA family of two closely related chironomids,Chironomus thummi thummi andCh. thummi piger (Diptera) by density-gradient centrifugation,melting analysis and restriction analysis

The DNAs of the two subspecies ofChironomus thummi, Ch. th. thummi andCh. th. piger, were investigated by CsCl density-gradient centrifugation, melting analysis and restriction analysis including Southern hybridization with AT-rich, highly repetitive DNA sequences. The melting analysis of density-fractionatedCh. th. thummi andCh. th. piger DNA has shown that thethummi DNA contains an early melting DNA fraction, which is enriched in the light fractions of the density gradient. The DNA fraction is also present inpiger DNA though in lower concentration. Restriction and Southern analysis of density fractionatedthummi andpiger DNA has revealed that there are two tandemly-repetitive DNA-sequence families that hybridize with this AT-rich, early melting DNA fraction. One sequence is characterized by anHae-III site and a basic repeat length of 130 ± 15 bp and the other by aCla-1 restriction site and a basic repeat length of 120 ± 4 bp. These sequences are present in much higher concentrations in the genome ofCh. th. thummi when compared toCh. th. piger, and are hence correlated to the higher DNA content of theCh. th. thummi genome.     

N-banding in polytene chromosomes of Chironomus and Drosophila

The N-banding patterns of the polytene chromosomes of Drosophila melanogaster, Chironomus melanotus, Ch. th. thummi and Ch. th. thummi x Ch. th. piger were studied. In Chironomus the polytene N-banding patterns correspond to the polytene puffing patterns. This is revealed by comparison of the puffing and N-banding patterns of identical chromosomes. Size and staining intensity of the N-bands reflect the size of the puffs as shown by puff induction. There is no evidence that the N-bands are also located in Chironomus heterochromatin or are restricted to the nucleolar organizer regions. In Drosophila the -heterochromatin is strongly N-positive, whereas the -heterochromatin, as well as the Chironomus heterochromatin is not N-banded. Contrary to Chironomus, the puffs in Drosophila polytene chromosomes do not give rise selectively to well stained N-bands. — The N-banding method is interpreted to stain specifically non-histone protein which is (1) accumulated in genetically active chromosome regions and (2) present in a specific type of heterochromatin (-heterochromatin of Drosophila).     

Different repetition frequencies of a 120 base-pair DNA-element and its arrangement in Chironomus thummi thummi and Chironomus thummi piger

The repetition frequency of a highly repetitive DNA sequence has been measured in the genomes of Ch. thummi thummi and Ch. th. piger. This sequence is known to be involved in the evolutionary duplication of defined chromosomal segments leading to a significant increase in the genome size of Ch. th. thummi. Reassociation of this highly repetitive DNA sequence which has a repeat length of 120 base-pairs, with total Ch. th. thummi and Ch. th. piger DNA has shown that the repetition frequency in the Ch. th. thummi DNA is 5.5 fold higher than in Ch. th. piger. In both genomes a 120 base-pair sequence is present as tandemly repeated sequence as shown by Southern analysis.     

Molecular evolutionary analysis of theywvz/7B globin gene cluster of the insectChironomus thummi

We report the sequence of 8.1 kb of DNA containing the 3 end of one and seven other complete intronless globin genes from theywvz/7B locus of the dipteranChironomus thummi thummi. One of these (cttv) appears to be a pseudogene by virtue of a premature termination codon, whereas the others encode apparently functional globin polypeptides. Taken together with previously published data, theC. th. thummi ywvz/7B locus codes for at least 11 globins, five of which differ from one another by no more than two amino acids. In contrast, only nine globin genes are found in a comparable genomic clone isolated fromC. th. piger. As indicated by sequence alignment, this difference in copy number can be attributed to a loss of one gene (fusion of globin genes 7B8 and 7B10) in thepiger lines, coupled with a gain (globin gene 7139) in thethummi lineage. Comparisons between thethummi andpiger sequences showed thatywvz/713 intergenic regions have maintained a level of 91 % similarity since thethummi/piger divergence: most differences are simply due to single base substitutions or insertion/deletion events in either thethummi or thepiger DNA, but three instances of partially overlapping deletions were also detected. A phylogenetic analysis ofywvz/713 gene products was conducted, from which a plausible reconstruction of the evolutionary history of the locus was obtained. In addition, alignment of globin 7B amino acid sequences suggested that globin genes 7B2 and 7B3 (reported at the protein and cDNA level, respectively, but not contained on theC. th. thummi orC. th. piger genomic clones) are possibly chimeric genes. Given the trend toward expansion of theC. thummi globin gene family in general and of the globin 7B subfamily in particular, we propose that increased copy number of these genes has been positively selected as a mechanism to achieve a high Hb concentration in the larval hemolymph. Correspondence to: G. Bergtrom     

Prolongation of replication time after doublings of the DNA content of polytene chromosome bands of Chironomus

Using ³H-thymidine autoradiography, labeling frequency of homologous asynapsed chromosome bands of the hybrid of Chironomus th. thummi and Chironomua th. piger has been studied. In a number of these bands the DNA content of the thummi bands is 2, 4, 8 or 16 times as large as that of the homologous piger bands (Keyl, 1965). Those bands of Ch. th. thummi which show one doubling of their DNA content in comparison with the homologous piger bands are also labeled two times more frequently than piger. In contrast to this such a correlation between increase of labeling frequency (i.e. prolongation of replication time) and doubling of the DNA content is not observed, when thummi bands have 4, 8 or 16 times more DNA than their homologues in piger. In these cases replication time is also prolonged after each doubling. Duration of DNA synthesis increases linearly but always by a smaller factor as the corresponding DNA content is increased.     

Differential staining of polytene chromosome bands in Chironomus by Giemsa banding methods

Two Giemsa banding methods (C banding and RB banding) are described which selectively stain the centromere bands of polytene salivary gland chromosomes in a number of Chironomus species. — By the C banding method the polytene chromosome appearance is changed grossly. Chromosome bands, as far as they are identifiable, are stained pale with the exception of the centromere bands and in some cases telomeres, which then are intensely stained reddish blue. — By the RB method the centromere bands are stained bright blue, whereas the remainder of the polytene bands stain red to red-violet. — Contrary to all other species examined, in Chironomus th. thummi numerous interstitial polytene chromosome bands, in addition to the centromere regions, are positively C banded and blue stained by RB banding. In the hybrid of Ch. th. thummi x Ch. th. piger only those interstitial thummi bands which are known to have a greater DNA content than their homologous piger bands are C banding positive and blue stained by the RB method whereas the homologous piger bands are C banding negative and red stained by RB banding. Ch. thummi and piger bands with an equal amount of DNA both show no C banding and stain red by RB banding. — It seems that the Giemsa banding methods used are capable of demonstrating, in addition to centromeric heterochromatin, heterochromatin in those interstitial polytene chromosome bands whose DNA content has been increased during chromosome evolution.     

Die Anaerobiose-Toleranz der Larven zweier Subspezies von Chironomus thummi

Zusammenfassung Die Anaerobiose-Toleranz der Larven zweier nahverwandter Subspezies der Gattung Chironomus wurde in einer mit Stickstoff (reinst) beschickten Warburg-Apparatur bei 20 und 25° C in kurzfristigen Versuchen (8, 12 und 24 Std) geprüft.Im Süßwasser besitzen die beiden Subspezies Chironomus thummi thummi und Chironomus thummi piger signifikante Unterschiede in ihrer Anaerobiose-Toleranz. Während die piger-Larven eine 24stündige N₂-Behandlung (bei 25° C) nicht überleben, tolerieren sie die thummi-Larven zu etwa 50 %.Die beiden Subspezies zeigen während der Anaerobiose im Süßwasser eine erhebliche Zunahme ihres Wassergehaltes, die in Korrelation zu den Absterberaten bei piger wesentlich schneller als bei thummi erfolgt. Gleichzeitig sinkt der osmotische Wert des Blutes, und zwar in dem gleichen Umfang, wie der Wassergehalt zunimmt. Eine deutliche Erhöhung der Blutkonzentration durch Spaltprodukte des anaeroben Stoffwechsels liegt nicht vor.Im annähernd blutisotonischen Brackwasser von 8%. S tolerieren beide Subspezies eine 24stündige N₂-Behandlung (bei 25° C); ihr Wasserhaushalt ist unter diesen Bedingungen nahezu ungestört.Die gegenüber Chironomus plumosus geringe Anaerobiose-Toleranz der thummi- und piger-Larven im Süßwasser ist daher auf eine gestörte Regulation des Wasserhaushaltes zurückzuführen.Die quantitativen physiologischen Differenzen zwischen den beiden Subspezies werden im Hinblick auf die unterschiedliche ökologische Einnischung sowie die korrespondierenden physiologischen Mechanismen diskutiert.Für ihre weitgehende ökologische Isolation — Ch. th. piger bevorzugt sauerstoffreichere eutrophe Kleingewässer als Ch. th. thummi — sind die quantitativen Unterschiede in der Anaerobiose-Toleranz wichtig.Mit Unterstützung der Deutschen Forschungsgemeinschaft.     

Cotransposition of a highly repetitive DNA element with flanking sequences in the genome of the midgeChironomus thummi

Summary A family of highly repetitive DNA elements, the Cla-elements, is present in the genomes of the two sibling speciesChironomus th. thummi andCh. th. piger. These Cla-elements are organized in large tandem repetitive clusters as well as occuring as interspersed monomeric elements, in both subspecies. The analysis of a monomeric Cla-element and several kilobases of its flanking sequences fromCh. th. piger revealed that the short Cla-elements are cotransposed together with adjacent DNA. We found the same association of Cla-elements with specific flanking DNA in clones obtained from the rDNA ofCh. th. thummi and from nonribosomal Cla-DNA ofCh. th. piger. The Cla-element-flanking DNA is clearly also repetitive, but mainly of inter-spersed organization.     

Homology of Balbiani rings among chironomid species and localization of a new mobile element on the polytene chromosomes

The results ofin situ cross-hybridization of the cloned DNA fragments of BRa, BRb and BRc fromChironomus thummi to the polytene chromosomes of 14Chironomus species andCamptochironomus tentans are presented. BRs of the species studied were demonstrated to contain the homologus DNA sequences. The cloned fragment from the BRa ofC. thummi hybridized with the BRa ofC. piger and with a region on the arm G ofC. tentans andC. plumosus, the latter species had no extra BR. The clone 16 from the BRb ofC. thummi hybridized only with the developed BR on the arm G of all species studied. The sequence from the BRc ofC. thummi was located in the BRc ofC. piger and in the developed BR ofC. plumosus andC. nuditarsis, which were located at the most distal end of arm G. These clones can be used as markers of homologous BRs. The new mobile elements C6.10 fromC. thummi genome were localized on the polytene chromosomes of 10Chironomus species andCamptochironomus tentans. The species of the generaLipiniella, Cryptochironomus andGlyptotendipes did not contain the sequences homologous to ME C6.10.     

DNS-Replikationsmuster der Speicheldrüsen-Chromosomen von Chironomiden

The pattern of DNA-synthesis of the salivary gland chromosomes of Chironomus thummi thummi, Ch. th. piger, Ch. annularius, Ch. plumosus and Ch. melanotus was studied using H³-thymidine-autoradiography. Contrary to the previous conception the bands of the salivary gland chromosomes of Chironomus do not begin replication simultaneously. H³-thymidine incorporation in bands of high DNA content begins later than in bands with a lesser amount of DNA. This difference in time is very small in bands outside the kinetochore regions and not comparable to the asynchrony in replication of typical heterochromatin in the salivary gland chromosomes of Chironomus melanotus. Differences in the amount of DNA in homologous bands do not affect the onset of replication. — Bands of high DNA content are replicating during a longer time than those having less DNA. However, certain chromosome regions behave differently. In these regions bands of very low DNA content are synthesizing DNA during the whole replication cycle. Since no excessive increase of DNA could be observed in these regions it is supposed that in addition to the duplication of structural DNA an extra DNA is synthesized which disappears immediately from the chromosome. — At the end of the replication cycle in the salivary gland nuclei of the hybrid Chironomus th. thummi X Ch. th. piger a labeling pattern is found in the chromosomes of Ch. th. thummi which differs from that in the parental subspecies Ch. th. thummi.     

Crossing over bei Bastarden von Chironomus thummi piger × Ch. thummi thummi

Zusammenfassung Bastarde mit der Elternkombination Chironomus thummi piger x Chironomus thummi piger wurden mit beiden Geschlechtern von Ch. th. piger rückgekreuzt. An den Speicheldrüsen-Chromosomen von 1401 Larven der Nachkommenschaft wurde die crossing over-Häufigkeit in den strukturidentischen und strukturdifferenten Chromosomenabschnitten in der Meiose der Bastarde untersucht.In den strukturdifferenten Chromosomenabschnitten der Bastarde ist die Austauschhäufigkeit erheblich niedriger (Chromosom I 1,6%, Chromosom II 0,4%, Chromosom III 0,2%, Chromosom IV 7,2%) als in den strukturidentischen Abschnitten (zwischen 20,6 und 38,4%). Regionen mit starken Strukturdifferenzen im Bastard (Chromosom III) haben seltener Austausch als Regionen mit schwachen Strukturdifferenzen (Chromosom IV). Bei Weibchen liegen die Austauschhäufigkeiten in den strukturidentischen Abschnitten höher als bei Männchen.Das Fehlen einer totalen Unterdrückung des Austausches in den strukturdifferenten Abschnitten bei Bastarden läßt auf eine untergeordnete Bedeutung cytogenetischer Faktoren als Isolationsmechanismus bei der Evolution beider Unterarten schließen.Mit Unterstützung der Deutschen Forschungsgemeinschaft.     

Complex Evolution of Tandem-Repetitive DNA in the Chironomus thummi Species Group

The subspecies Chironomus thummi thummi and C. t. piger display dramatic differences in the copy number and chromosomal localization of a tandemly repeated DNA family (Cla elements). In order to analyze the evolutionary dynamics of this repeat family, we studied the organization of Cla elements in the related outgroup species C. luridus. We find three different patterns of Cla element organization in C. luridus, showing that Cla elements may be either strictly tandem-repetitive or be an integral part of two higher-order tandem repeats (i.e., Hinf[lur] elements, Sal[lur] elements). All three types of Cla-related repeats are localized in the centromeres of C. luridus chromosomes. This suggests that the dispersed chromosomal localization of Cla elements in C. t. thummi may be the result of an amplification and transposition during evolution of this subspecies. Received: 22 May 1996 / Accepted: 8 October 1996     

Hybrid dysgenesis in Drosophila melanogaster: influence of temperature on cytotype determination in the P-M system

Summary In Drosophila melanogaster, the P-M system of hybrid dysgenesis is a syndrome of germ line abnormalities, including temperature dependent gonadal dysgenesis (GD sterility), high rates of mutation and male recombination, which occurs in some interstrain hybrids but only from one of the two crosses. In the P-M system, hybrid dysgenesis results from interaction between chromosomally transposable elements of the P element family and a particular extrachromosomal state referred to as the M cytotype. Cytotype (M or P) is known to be determined by the absence or presence of chromosomal factors, but principally with limited cytoplasmic transmission.In a series of experiments in which F1 hybrid females from various P and M strains were submitted to different preadult and ageing temperature treatments, it was found that the cytotype switch is strongly temperature-dependent in the F1 females from M x P but not in the reciprocal cross. In the F1 females from the former cross, a strong M cytotype occurs at a low developmental temperature (18° C) and a weak M cytotype occurs at a high developmental temperature (26.5° C). On the other hand, a high ageing temperature applied after a low developmental temperature switches the cytotype from M to P and reciprocally, a low ageing temperature applied after a high developmental temperature switches the cytotype from P to M.This thermo-reversibility of the extrachromosomal state exists only in the F1 females from M mothers but not in the F1 females from P mothers; this dissymmetrical behavior is discussed in relation to the mechanism proposed by O'Hare and Rubin (1983) which explains cytotype determination by a positive feedback of the regulator of the P transposase on its own level of activity.