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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular evolution 41 (1995), S. 909-919 
    ISSN: 1432-1432
    Keywords: Hemoglobins ; Chironomus ; Kiefferulus ; Gene clusters ; Molecular evolution
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A genomic clone containing hemoglobin genes was isolated from a species of the chironomid genus Kiefferulus. Eight genes, including an apparent pseudogene, were sequenced and the amino acid sequences of the putative proteins were determined. By comparison to the previously described hemoglobins in the sister-genus Chironomus, they were identified as members of the dimeric Hb VIIB group. The results indicate that the existence of clusters of hemoglobin genes may be a common feature in chironomids and not just confined to Chironomus. The Kiefferulus genes show greatest similarity of amino acid sequence to Hb VIIB-7 from the Chironomus cluster. The results suggest that the ancestral cluster contained at least two gene types, one of which gave rise to VIIB-7 and the Kiefferulus genes while the other gave rise to the other Chironomus VIIB genes. Both clusters appear to have increased in size by duplication or unequal crossing over since the separation of the genera. It also appears that an unrelated gene present in the Chironomus cluster, Hb-Y, arose from a completely independent origin with no apparent equivalent gene anywhere in the genome of Kiefferulus or some other Chironomus species.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1432
    Keywords: Key words: Silk proteins — Cysteine-rich modular proteins — Balbiani ring genes — Glycosylation —Synonymous substitutions –Nonsynonymous substitutions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract. Aquatic larvae of the midge, Chironomus tentans, synthesize a 185-kDa silk protein (sp185) with the cysteine-containing motif Cys-X-Cys-X-Cys (where X is any residue) every 20–28 residues. We report here the cloning and full-length sequence of cDNAs encoding homologous silk proteins from Chironomus pallidivittatus (sp185) and Chironomus thummi (sp220). Deduced amino acid sequences reveal proteins of nearly identical mass composed of 72 blocks of 20–28 residues, 61% of which can be described by the motif X5–8-Cys-X5-(Trp/Phe/Tyr)-X4-Cys-X-Cys-X-Cys. Spatial arrangement of these residues is preserved more than surrounding sequences. cDNA clones enabled us to map the genes on polytene chromosomes and identify for the first time the homolog of the Camptochironomus Balbiani ring 3 locus in Chironomus thummi. The apparent molecular weight difference between these proteins (185 vs 220 kDa) is not attributable to primary structure and may be due to differential N-linked glycosylation. DNA distances and codon substitutions indicate that the C. tentans and C. pallidivittatus genes are more related to each other than either is to C. thummi; however, substitution rates for the 5′- and 3′-halves of these genes are different. Blockwise sequence comparisons suggest intragenic variation in that some regions evolved slower or faster than the mean and may have been subjected to different selective pressures.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Chromosoma 45 (1974), S. 91-98 
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Analysis of the banding pattern of the salivary gland chromosomes of Chironomus tepperi indicates that, despite a somewhat modified male hypopygium, the relationships of this species are close to the other Australian species of the genus, particularly to Ch. oppositus. No inversion polymorphism has been found in Ch. tepperi and this, together with the relatively high chiasma frequency as measured at metaphase I, would appear to be an adaptation to provide genetic variability necessary for its colonizing ability.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Chromosoma 35 (1971), S. 418-430 
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Two cytologically distinguishable species have been found in material ofChironomus australis. These species have been calledCh. australis andCh. duplex. Both belong to thepseudothummi-cytological grouping because they have the chromosome arm combinations AE, BF, CD, G.Ch. duplex shows a modified arm pattern due to a tandem fusion of arm G to arm E.—The banding patterns of the polytene chromosomes of the two species are compared to each other and to the Australian standard species,Ch. oppositus. Ch. australis is very close cytologically toCh. oppositus, whileCh. duplex, which is considered a derived species because of the tandem fusion, shows a number of inversion differences from the morphologically similarCh. australis. Ch. duplex is polymorphic for six inversions, four of which are simple inversions, the other two are complex involving also the transposition of some bands.Ch. australis appears to be monomorphic.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-0886
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Abstract Sex determination in a group of phylogenetically related Chironomus species, of the pseudothummi complex, from south-eastern Australia and New Zealand is male heterogametic, controlled by a male determiner. The male determiner has been located at least to the level of the chromosome arm in most members of this phylogenetic group. It varies in location among many of the species and there are some phylogenetic patterns discernable, which are discussed in relation to the possible origin of the sex determiner. There is a group of species, Ch. oppositus ff. oppositus and whitei, Ch. australis, Ch. alternans a and Ch. alternans c, which appear to be central to this phylogeny, in which the sex determiner is located near the centromere of the CD chromosome, the most common location in the Australasian group. This is different from the most common location, arm F, of the thummi complex in Europe and North America. There is also a group, comprising Ch. oppositus f. tyleri, Ch. cloacalis, Ch. alternans b and Ch. nepeanensis, in which the sex determiner is on arm G. The arm A sex determiners, found in Ch. tepperi, Ch. oppositus ff. whitei and connori, and Ch. occidentalis, may be of common origin or they may be independently derived, as must be the arm B (Ch. duplex) and arm F (Ch. oppositus f. whitei) sex determiners. In Ch. oppositus f. whitei, four different chromosomal locations for the sex determiner have been identified. It is not yet clear whether these represent an unstable polymorphism or indicate the existence of cryptic subgroupings within this form. Although the location of the sex determiners can be assigned to particular chromosome arms, the precise location cannot be determined, therefore the assumption of common origin may not always be correct. Also, this uncertainty means that it is impossible at present to differentiate between a complex system of sex determination and the possibility of a translocatable sex determiner as explanations of the variability in sex determiner location. The forms of Ch. oppositus are redefined and renamed to avoid confusion caused by the previous names.
    Type of Medium: Electronic Resource
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