The karyotype of Brachyteles arachnoides (E. Geoffroy, 1806) (Primates: Platyrrhini)

The karyotype of one female Brachyteles arachinoides (E. Geoffroy, 1806) was studied. The specimen exhibited 62 chromosomes, which could be arranged in three clearly distinguishable groups: the first one including 5 pairs of subtelocentric chromosomes, the second one including 8 pairs of metacentric and submetacentric chromosomes and the third one including 18 pairs of acrocentric chromosomes. The X chromosome pair could not be identified.This study was supported by grants from CNPq (SIP 04/011), Brazil.     

Chromomycin, mithramycin, and olivomycin binding sites on heterogeneous deoxyribonucleic acid. Footprinting with (methidiumpropyl-EDTA)iron(II)

The DNA binding sites for the antitumor, antiviral, antibiotics chromomycin, mithramycin, and olivomycin on 70 base pairs of heterogeneous DNA have been determined by using the (methidiumpropyl-EDTA)iron(II) [MPE x Fe(II)] DNA cleavage inhibition pattern technique. Two DNA restriction fragments 117 and 168 base pairs in length containing the lactose operon promoter-operator region were prepared with complementary strands labeled with 32P at the 3' end. MPE x Fe(II) was allowed to partially cleave the restriction fragment preequilibrated with either chromomycin, mithramycin, or olivomycin in the presence of Mg2+. The preferred binding sites for chromomycin, mithramycin, and olivomycin in the presence of Mg2+ appear to be a minimum of 3 base pairs in size containing at least 2 contiguous dG x dC base pairs. Many binding sites are similar for the three antibiotics; chromomycin and olivomycin binding sites are nearly identical. The number of sites protected from MPE x Fe(II) cleavage increases as the concentration of drug is raised. For chromomycin/Mg2+, the preferred sites on the 70 base pairs of DNA examined are (in decreasing affinity) 3'-GGG, CGA greater than CCG, GCC greater than CGA, CCT greater than CTG-5'. The sequence 3'-CGA-5' has different affinities, indicating the importance of either flanking sequences or a nearly bound drug.     

The C-banded karyotypes of the four British species of Notonecta L. (Heteroptera: Notonectidae)

Chromosome preparations were made from mid-gut and ovarian cells of adult Notonecta glauca L., N. obliqua Thunberg, N. maculata F. and N. viridis Delcourt, using the acetic acid dissociation, air-drying method (Crozier 1968) with Giemsa staining. C-banding was obtained by treatment with barium hydroxide and salt-sodium citrate (2xSSC). The karyotypes of the first three species are very similar, with 11 pairs of autosomes plus XY sex chromosomes (plus sometimes a small 12th autosome pair in N. glauca), and the sequence of chromosome sizes very similar. However, the four longest pairs of autosomes, and the X chromosomes, have characteristic C-band patterns, which differ between the species. The karyotype of N. viridis is more distinct, with one pair of long autosomes, while the remaining chromosomes are much shorter. The long autosomes have distinct C-bands, but these are present in only one of the shorter pairs, as faint terminal bands. In warm conditions the long autosomes of N. viridis appear rod-like, but in cold conditions they have one end heavily condensed, giving a tadpole-like appearance.     

Nucleolar behavior during meiosis in four species of phyllostomid bats (Chiroptera, Mammalia)

We analyzed the behavior of the nucleolus, nucleolar structures and nucleolus organizer regions (NORs) during meiotic division in four species of phyllostomid bats that have different numbers and locations of NORs. Nucleoli began disassembly at leptotene, and the subcomponents released from the nucleolus were dispersed in the nucleoplasm, associated with perichromosomal regions, or they remained associated with NORs throughout division. In Phyllostomus discolor, a delay in nucleolus disassembly was observed; it disassembled by the end of pachytene. The RNA complexes identified by acridine orange staining were observed dispersed in the nucleoplasm and associated with perichromosomal regions. FISH with rDNA probe revealed the number of NORs of the species: one NOR in Carollia perspicillata, one pair in Platyrrhinus lineatus and P. discolor, and three pairs in Artibeus lituratus. During pachytene, there was a temporary dissociation of the homologous NORs, which returned to pairing at diplotene. The variation in the number (from one to three pairs) and location of NORs (in sex or autosomal chromosomes, at terminal or interstitial regions) did not seem to interfere with the nucleolar behavior of the different species because no variation in nucleolar behavior that could be correlated with the variation in the number and chromosomal location of NORs was detected.     

Features of two hepatitis B virus (HBV) DNA integrations suggest mechanisms of HBV integration.

Two integrated hepatitis B virus (HBV) DNA molecules were cloned from two primary hepatocellular carcinomas each containing only a single integration. One integration (C3) contained a single linear segment of HBV DNA, and the other integration (C4) contained a large inverted duplication of viral DNA at the site of a chromosome translocation (O. Hino, T.B. Shows, and C.E. Rogler, Proc. Natl. Acad. Sci. USA 83:8338-8342, 1986). Sequence analysis of the virus-cell junctions of C3 placed the left virus-cell junction at nucleotide 1824, which is at the 5' end of the directly repeated DR1 sequence and is 6 base pairs from the 3' end of the long (L) negative strand. The right virus-cell junction was at nucleotide 1762 in a region of viral DNA (within the cohesive overlap) which shared 5-base-pair homology with cellular DNA. Sequence analysis of the normal cellular DNA across the integration site showed that 11 base pairs of cellular DNA were deleted at the site of integration. On the basis of this analysis, we suggest a mechanism for integration of the viral DNA molecule which involves strand invasion of the 3' end of the L negative strand of an open circular or linear HBV DNA molecule (at the DR1 sequence) and base pairing of the opposite end of the molecule with cellular DNA, accompanied by the deletion of 11 base pairs of cellular DNA during the double recombination event. Sequencing across the inverted duplication of HBV DNA in clone C4 located one side of the inversion at nucleotide 1820, which is 2 base pairs from the 3' end of the L negative strand. Both this sequence and the left virus-cell junction of C3 are within the 9-nucleotide terminally redundant region of the HBV L negative strand DNA. We suggest that the terminal redundancy is a preferred topoisomerase I nicking region because of both its base sequence and forked structure. Such nicking would lead to integration and rearrangement of HBV molecules within the terminal redundancy, as we have observed in both our clones.     

Neotropical Monogenoidea. 33. Three new species of Ancistrohaptor n. g. (Dactylogyridae,Ancyrocephalinae) on Triportheus spp. (Teleostei,Characidae) from Brazil,with checklists of ancyrocephalines recorded from neotropical characiform fishes

Three new species of Ancistrohaptor n. g. are described from the gills of three species of Triportheus (Characidae) collected from the environs of Manaus, Amazonas, Brazil: A. falcatum n. sp. from T. elongatus; and A. falciferum n. sp. and A. falcunculum n. sp. from T. angulatus, T. albus and T. elongatus. Ancistrohaptor n. g. is proposed for species possessing overlapping gonads, a dextral or dextroventral vaginal aperture, a coiled (counter-clockwise) male copulatory organ, two accessory pieces in the copulatory complex, and a haptor armed with two pairs of anchors (ventral anchor with elongate shaft), dorsal and ventral bars and 14 hooks; hook pair 1 (ventral) anterior to ventral bar, pairs 2–4 (ventral) lying bilaterally anterior to ventral anchor bases, pair 5 (ventral) associated with distal end of ventral anchor shafts, and pairs 6 and 7 (dorsal) bilateral about midway along haptoral length. Parasite-host and host-parasite lists of the Ancyrocephalinae from neotropical Characiformes are provided.     

DNA and chromatin structure of the human alpha 1 (I) collagen gene

The human alpha 1 (I) collagen gene and 48 kilobase pairs of flanking DNA have been isolated on two overlapping cosmids. The alpha 1 (I) gene is 18 kilobase pairs long and contains a single repetitive element of the Alu family; at least 15 repetitive elements are present in the flanking DNA. Analysis of chromatin structure in nuclei isolated from cultured fibroblasts demonstrated a single chromatin domain greater than 65 kilobase pairs in length that contained 9 DNase I-hypersensitive sites. The pattern of hypersensitive sites was also determined in nuclei derived from placental tissue. Five of the DNase I-hypersensitive sites were observed in both placental and fibroblast chromatin including one site near the 5' end and another near the 3' end of alpha 1 (I). An additional two sites located near the 3' end of the alpha 1 (I) gene in fibroblast chromatin are associated with the tissue-specific use of different polyadenylation sites. Two DNase I-hypersensitive sites found only in fibroblast chromatin and one site found only in placental chromatin were located more than 10 kilobase pairs away from the alpha 1 (I) gene and may be related to tissue-specific expression of other genes in the domain. However, the only abundant placental mRNAs from the 65-kilobase pair domain were those transcribed from the alpha 1 (I) gene. These findings suggest that physical linkage does not play a predominant role in controlling coordinate expression of collagen genes.     

荔枝SSR标记的研究

以无核荔枝A4号为实验材料,应用选择性扩增微卫星（SAM）法分离、克隆了100个简单序列重复（SSR）序列,其中88个非重复,可用。加上搜索数据库所获得的1个SSR序列,一共89个序列用于特异引物的设计。仅从71个序列的82个基因座设计出特异引物。合成41条特异引物(与5′锚定简并引物配对,个别相互配对),对其中的39个基因座进行检测。其中15对引物扩增出相应大小的片段,另外11对引物扩增出非预期片段。最后,以37个荔枝种质的基因组DNA为模板,从26对出带的引物中,筛选出多态性引物21对,获得了22个荔枝基因座特异性SSR标记。     

Molinacuaria indonesiensis n. sp. (Nematoda,Acuarioidea) from Rattus argentiventer in Indonesia

Molinacuaria indonesiensis n. sp. from the stomach of Rattus argentiventer, the ricefield rat, in Sukamandi, Java, Indonesia is described and figured from the examination of seven males and three females. The species is separated from the three other species of the genus, namely, M. bendelli (Adams & Gibson, 1969) Wong & Lankester, 1985, M. acholonui (Schmidt & Kuntz, 1972) Wong & Lankester, 1985 and M. gallinulae (Wang, 1966) Wong & Lankester, 1985. The species is characterised by (i) the larger body measurements, (ii) the presence of a fold rather than a deep groove separating the anterior cephalic region and the ptilina which form four distinct shields, (iii) the morphology of the four ptilina, each one being tripartite with a pointed middle section twice as long at the two lateral sections (iv) the number of papillae on the posterior end of the male (two pairs pre-cloacal, four pairs post-cloacal), (v) the morphology of the left spicule, and (vi) the female tail being straight with a terminal knob.     

Redescription of Hemiclepsis quadrata (Moore, 1939) n. comb. (Hirudinea: Glossiphoniidae)

Hemiclepsis quadrata, which is the only representative of the genus so far reported in Africa, is redescribed. Illustrations showing the diagnostic features of the taxon are provided for the first time. A thorough study of the holotype and one of the paratypes, as well as additional specimens, revealed that Moore overlooked certain important taxonomic features when he described the leech as a Batracobdella species. The transfer of this species to the genus Hemiclepsis is based on the following features exhibited by this leech: dilated head region, three pairs of eyes, central proboscis pore, ten pairs of crop caeca and small genital atria.     

Chromosome number and karyotype of Donax trunculus L. (Mollusca,Bivalvia, Tellinacea)

A chromosome study of Donax trunculus was made with specimens collected from a population of the French Atlantic coast. The karyotype, not previously described, consists of 19 pairs of chromosomes (2n=38) as in the majority of the species so far investigated in the Veneroida. There was no evidence of morphologically identifiable heterosomes. The karyotype is characterized by (1) a high total chromosome length which reaches 228.56 m, (2) a great heterogeneity of the chromosome length, and (3) a high number of meta- and submetacentrics, 9 and 7 pairs respectively vs. 3 pairs of subtelocentrics, giving a fundamental number of 70. Comparison with two other closely related families having reported karyological data-Scrobiculariidae and Semelidae-suggests that, although chromosome numbers are identical, the karyotype is clearly different from one family to the other.     

Heterochromatic marker regions (nucleolar organisers) in the chromosomes of the common mussel,Mytilusedulis (Mollusca : Pelecypoda)

The chromosomes of Mytilus cdulis were studied using chromosome banding (G- and C-banding) and silver (Ag-) staining techniques. Four pairs of chromosomes, out of the total complement of 14 pairs, were characterized by the presence of conspicuous, G-band negative/C-band positive, heterochromatic regions terminal to their long arms. The affected chromosomes were identified as pairs 1, 8, 11, and 14. Ag-staining revealed that these heterochromatic regions were also the sites of the nucleolar organiser regions (NORs): the specific gene sequences responsible for coding for ribosomal RNA, and which function as the morphological sites around which nucleoli develop at the end of mitosis. In common with other species, including man, there was considerable inter-cell variation in this character, which was probably a reflection of the variation in the specific activity of these regions in terms of rRNA protein synthesis.     

Observations on a cucullanid nematode of marine fishes from Taiwan Strait, Dichelyne (Cucullanellus) jialaris n. sp

During a helminthological examination of marine fishes from south of the Minnan-Taiwan Bank Fishing Ground, Taiwan Strait, Fujian, China, a new cucullanid nematode, Dichelyne (Cucullanellus) jialaris n. sp., was removed from the intestine of the red seabream, Pagrus major (Temminck & Schlegel, 1834). The new species differs from its congeners mainly in the following characters: body size medium but with relative long spicules of 1.01 mm (0.97-1.06) in length or 20.0% (18.21-21.8%) of the body length; proximal end of spicules somewhat expanded and distal end rounded; gubernaculum I-shaped, slightly narrow in the middle part, both ends rounded; both anterior and posterior cloaca lips round or oval, prominent and unequal in size. The anterior cloaca lip is at least 2 times larger than the posterior one. There is a conspicuous papilliform structure within the central of anterior and posterior cloacal lip. Vulva of female is not prominent, slightly postequatorial; distance from vulva to anterior end of body is 4.3 (3.0-5.5) mm or 58.0% (54.0-62.0%) of the body length. Considering the result of comparing the structure of so-called unpaired median papilla with the 10 pairs of caudal petiolated papillae in the body of the same individual. the papilliform structures are just a backstop for the cloacal lips, this new species represents the first record of a nematode of the Dichelyne, subgenus Cucullanellus in marine fishes of China Sea.     

Scanning electron microscopic observations of adult Baylisascaris procyonis (Nematoda)

The scanning electron microscope was used to illustrate the microtopographic features of the caudal end of adult male Baylisascaris procyonis. The male tail was relatively long, smoothly attenuated and often had a small button-like or mucronate termination. The preanal papillae were situated ventrally in two slightly divergent and somewhat irregularly spaced rows. Anterior and posterior to the anus were two slightly raised roughened patches consisting of several rows of small spines. Just anterior to the anus along the outer margin of the preanal roughened patch was a large double medioventral papilla. There were five pairs of postanal papillae with the first pair just posterior to the anus being double while the remaining four pairs were more closely associated in a group near the tail end. The second pair were also double papillae; however, in a few specimens they were not fused and appeared as two single closely associated papillae. The last three pairs of papillae were single. The fourth pair of caudal papillae were the phasmids and in the center of each was a ringed pore-like opening. The spicules of the male had a highly sculptured surface with a pincher-like terminal end.     

Fine Structural Analysis of the Silk Apparatus in the Funnel-web Spider, Agelena limbata (Araneae: Agelenidae)

ABSTRACT Silk apparatus of the funnel-web spider, Agelena limbata was located at the ventral end of the abdominal part, and was composed of internal silk glands and external spinnerets. Among the three pairs of spinnerets, the posterior pairs were highly elongated along the body axis. By the light and electron microscopic inspections, it was found that four types of silk glands were connected through the typical spinning tubes of each spinneret. Anterior spinnerets comprise 2 pairs of the ampullate and 125 to 150 pairs (female) or 110 to 114 (male) of pyriform glands. Another 2 pairs of ampullate glands in both sexes, 5 to 8 pairs of tubuliform glands in females, and 20 to 26 pairs (female) or 15 to 17 pairs (male) of aciniform glands were connected on the median spinnerets. Additional 8 to 10 pairs of tubuliforms in female and 41 to 53 pairs (female) or 27 to 32 pairs (male) of aciniform glands were on the posterior spinnerets, respectively. While the ampullate and tubuliform glands were connected with the spigot-type spinning tubes, the pyriform and aciniform glands with that of spool-type tubes. It has been also revealed that the tubuliform glands were only observed in female spiders, however the flagelliform and aggregate glands which had the function of adhesive thread production in orb-web spiders were not observed at both sexes of this spiders.     

Cytogenetic characterisation of the razor shells Ensis directus (Conrad, 1843) and E. minor (Chenu, 1843) (Mollusca: Bivalvia)

The European razor shell Ensis minor (Chenu 1843) and the American E. directus (Conrad 1843) have a diploid chromosome number of 38 and remarkable differences in their karyotypes: E. minor has four metacentric, one metacentric–submetacentric, five submetacentric, one subtelocentric and eight telocentric chromosome pairs, whereas E. directus has three metacentric, two metacentric–submetacentric, six submetacentric, six subtelocentric and two telocentric pairs. Fluorescent in situ hybridisation (FISH) using a major ribosomal DNA probe located the major ribosomal genes on one submetacentric chromosome pair in both species; FISH with a 5S ribosomal DNA (5S rDNA) probe rendered one chromosomal (weak) signal for E. minor and no signal for E. directus, supporting a more dispersed organisation of 5S rDNA compared to the major ribosomal genes. The vertebrate telomeric sequence (TTAGGG) _n was located on both ends of each chromosome, and no interstitial signals were detected. In this work, a comparative karyological analysis was also performed between the four Ensis species analysed revealing that the three European species studied so far, namely E. minor, E. siliqua (Linné 1758) and E. magnus Schumacher 1817 show more similarities among them than compared to the American species E. directus. In addition, clear karyotype differences were found between the morphologically similar species E. minor and E. siliqua.     

Ultrastructure of the labrum and foregut of Derocheilocaris remanei (Crustacea,Mystacocarida)

The cuticle-lined foregut of Derocheilocaris remanei consists of the mouth with its associated labrum, and an undifferentiated esophagus. It is separated from the midgut by an esophageal valve. The labrum is a conspicuous structure moved by five pairs of muscles (four dorsoventral and one longitudinal). Four pairs of subcuticular glands open to its inner face forming two longitudinal, lateral rows of cuticular pores. Each secretory unit is composed of a glandular component (with one or two secretory cells), a neck cell, and a duct cell. In addition, a single gland cell opens mesially into the buccal cavity. The ventrally located mouth is a complex structure characterized by a filter-like system, a sensory organ, and epithelial cells with highly developed microvilli. The esophagus is a simple tube with a characteristic curvature following the mouth. It has a rounded cross section and a triradiate lumen. A layer of circular musculature surrounds this region. The end of the esophagus protrudes into the midgut lumen forming the so-called esophageal valve. The ultrastructural features of the foregut, with the presence of a mucus-trapping mechanism, a relatively well-developed filter system and associated structures and an esophagus lacking glands confirm the microphagic feeding habits of mystacocarids. © 1996 Wiley-Liss, Inc.     

Time and space distribution of coincident impulses in closed neural circuits in the sensorimotor cortex of the rabbit (the rhythmical defensive dominanta)

In the course of analysis of the conjugate unit activity of simultaneously recorded neurons in the sensorimotor cortex of rabbits, 22 closed neural circuits consisting of 3 or 4 neurons were considered. In the model of the defensive dominanta, 1-3 weeks after imposing rhythmic (2 s) activity to a rabbit, the distribution of coincident impulses was analyzed in real time. It was found out that the events when the coincident impulses of neural pairs were generated with two-second intervals could be shifted in time and space over a closed circuit of neurons in one direction. Two-second intervals between the coincident impulses of the neighboring pairs could be conjugate, i.e. the end of one interval in one pair coincided with the beginning of a two-second interval in the next pair. Conjugate intervals of the neighboring neural pairs could promote a pass-through of the information on the stimulus properties over the closed neuronal circuit, thus completing a full cycle. The longest passes-through lasted from 10 and 12 s. Also, more intricate variants of the information transfer were revealed. Thus, not only passes-through of the two- second intervals between the neuronal pairs were observed, but also, coincident impulses repeatedly occurred with this interval in some of the pairs of the circuits. The longest transitions lasted 16 and 22 s.     

Characterization of the chromosome complement of Helianthus annuus by in situ hybridization of a tandemly repeated DNA sequence.

A tandemly repeated sequence isolated from a clone (HAG004N15) of a nebulized genomic DNA library of sunflower (Helianthus annuus L., 2n = 34) was characterized and used to study the chromosome complement of sunflower. HAG004N15 repeat units (368 bp in length) were found to be highly methylated, and their copy number per haploid (1C) genome was estimated to be 7800. After in situ hybridization of HAG004N15 repeats onto chromosome spreads, signals were observed at the end of both chromosome arms in 4 pairs and at the end of only one arm in 8 other pairs. Signals were also observed at the intercalary (mostly subtelomeric) regions in all pairs, in both arms in 8 pairs, and in only one arm in the other 9 pairs. The short arm of 1 pair was labelled entirely. The chromosomal location of ribosomal DNA was also studied by hybridizing the wheat ribosomal probe pTa71. Four chromosome pairs contained ribosomal cistrons at the end of their shorter arm, but a satellite was seen in only 3 pairs. These hybridization patterns were the same in the 3 sunflower lines studied (HA89, RA20031, and HOR). The chromosomal localization of HAG004N15-related sequences allowed all of the chromosome pairs to be distinguished from each other, in spite of small size and similar morphology.     

Subunit IV (Mr = 14,384) of the cytochrome b-c1 complex from Rhodobacter sphaeroides. Cloning, DNA sequencing, and ubiquinone binding domain.

The Rhodobacter sphaeroides gene encoding subunit IV of the cytochrome b-c1 complex (fbcQ) was cloned and sequenced. The fbcQ cistron is 372 base pairs long and encodes 124 amino acid residues. The molecular mass of subunit IV, deduced from the nucleotide sequence, is 14,384 Da. A hydropathy plot of the predicted amino acid sequence revealed only one transmembrane helix; it is near the C-terminal end. The 3-azido-2-methyl-5-methoxy-6-(3,7-dimethyl[3H]octyl)-1,4-benzoquinone ([3H]azido-Q)-labeled subunit IV was isolated from the [3H]-azido-Q-treated cytochrome b-c1 complex. A ubiquinone-binding peptide was obtained by digesting the labeled subunit IV with V8 protease followed by high performance liquid chromatography separation. Amino acid analysis and partial N-terminal sequencing of this ubiquinone-binding peptide revealed that it corresponded to residues 77-124 of subunit IV. Based on the hydropathy profile and predicted tendency to form alpha-helices and beta-sheets, we propose a structural model for subunit IV. In this model the ubiquinone-binding domain is located near the surface of the membrane.