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H Mannen

Publications and source records attributed to H Mannen.

At least 19 recordsLinked to original sources
PubMed1998

Effect of mitochondrial DNA variation on carcass traits of Japanese Black cattle.

Japanese Black fattening steers were used to examine relationships between carcass traits and mitochondria displacement loop (D-loop) variations. The D-loop region of Japanese Black cattle was sequenced and revealed 26 mitochondrial haplotypes defined by 25 polymorphic sites. The haplotypes were classified into five mitochondrial types (type 1 to 5) using the unweighted pair-group method with arithmetic means. Carcass weight, longissimus muscle area (LMA), rib thickness, subcutaneous fat thickness, yield estimate, and beef marbling score (BMS) were compared among five mitochondrial types with BLUP procedures. Significant differences between mitochondria types were detected for LMA and BMS. Difference (P < . 05) was observed between mitochondrial types 2 and 4 for LMA. There was a highly significant difference (P < .01) in BMS between types 2 and 4. Difference (P < .05) was also found between types 1 and 4 on BMS. These results suggest that cytoplasmic genetic effects are important sources of variation for carcass traits in Japanese Black cattle.

Animals↗
PubMed1997

The cDNA cloning and molecular evolution of reptile and pigeon lactate dehydrogenase isozymes.

The cDNAs encoding lactate dehydrogenase isozymes LDH-A (muscle) and LDH-B (heart) from alligator and turtle and LDH-A, LDH-B, and LDH-C (testis) from pigeon were cloned and sequenced. The evolutionary relationships among vertebrate LDH isozymes were analyzed. Contrary to the traditional belief that the turtle lineage branched off before the divergence between the lizard/alligator and bird lineages, the turtle lineage was found to be clustered with either the alligator lineage or the alligator-bird clade, while the lizard lineage was found to have branched off before the divergence between the alligator/turtle and bird lineages. The pigeon testicular LDH-C isozyme was evidently duplicated from LDH-B (heart), so it is not orthologous to the mammalian testicular LDH-C isozymes.

Alligators and Crocodiles↗
PubMed1996

Cloning and expression of human homolog HSMT3 to yeast SMT3 suppressor of MIF2 mutations in a centromere protein gene.

A human HSMT3 cDNA encoding a homolog of the yeast SMT3, a suppressor of MIF2 mutations in a centromere protein gene, was identified and sequenced. The sequence of 95 amino acids deduced from the human HSMT3 cDNA exhibited 51.1% identity and 69.6% similarity to the yeast Smt3p sequence. The HSMT3 transcripts of 1.35Kb were found to be abundantly expressed in various human tissues.

Amino Acid Sequence↗
PubMed1995

Identification and minisatellite linkage analysis of SMXA recombinant inbred strains of mice by DNA fingerprinting.

SMXA recombinant inbred (RI) strains of mice were produced by systematic inbreeding from the F2 generation of a cross between two progenitor inbred strains, A/J and SM/J, which differ considerably with respect to many characteristics, and consists of 28 inbred strains. In this study, we investigated the applicability of DNA fingerprinting with M13 phage DNA to the identification of these closely related strains. DNA fingerprints of the SMXA RI strains and their progenitors, SM/J and A/J, showed strain-specific patterns, with the same banding patterns within each strain. Linkage analysis by using strain distribution patterns of minisatellite loci with 108 genetic markers containing microsatellites, biochemical and immunological marker genes allowed 23 minisatellite loci to be assigned to 11 chromosomes. The results suggested that DNA fingerprinting with M13 phage DNA is applicable not only for strain identification but also for genetic monitoring of RI strains on almost all chromosomes.

Animals↗
PubMed1995

The lactate dehydrogenase gene from nematode Caenorhabditis elegans contains only two of six introns conserved in the protein-encoding sequence of LDH genes from bird and mammals.

The protein-encoding region of L-lactate dehydrogenase (LDH) gene from nematode, Caenorhabditis elegans, was amplified by polymerase-chain-reaction from total genomic DNA and its nucleotide sequence determined. A comparison of this genomic sequence with the published sequence of nematode LDH cDNA reveals the presence of two introns of 57 and 47 nucleotides at codon no. 82 and 279-280, respectively. The positions of the two introns present in this invertebrate LDH gene correspond to the second and sixth introns of vertebrate LDH genes. The protein-coding sequence of human LDH-A (muscle), LDH-B (heart) and LDH-C (testis), mouse LDH-A, and duck LDH-B genes has previously been shown to be interrupted by six introns at the homologous positions.

Amino Acid Sequence↗
PubMed1994

Identification of sublines of inbred strains of mice and assessment of genetic relationships between substrains or sublines by DNA fingerprinting.

Identification of substrains or sublines of inbred mice and assessment of genetic relationships among them were performed on the basis of DNA fingerprinting using M13 phage DNA as a probe. We used eight C57BL/6 sublines (J parallel Jcl, J parallel Jms, J parallel Slc, J parallel Nrs, J parallel Yok, Jah, N parallel Crj, N parallel Jcl) and eleven C3H/He sublines, (J, J parallel Jcl, J parallel Yok, J parallel Nrs, J parallel Jms, N, N parallel Jcl, N parallel Crj, Slc, Jah, Nrs). Two kinds of restriction endonucleases (HinfI and PstI) were used. It was found that: 1) DNA fingerprint within each subline showed identical patterns. 2) Most sublines of C57BL/6 and C3H/He could be identified using DNA fingerprinting with HinfI except between N parallel Crj and Slc, and among J, J parallel Nrs and J parallel Yok in C3H/He. DNA fingerprints with PstI endonucleases showed low polymorphic banding patterns. 3) A dendrogram constructed from DNA fingerprint patterns reflected generally the genealogy of the sublines used. 4) DNA fingerprinting, therefore, seemed to be suitable for the genetic monitoring and assessment of genetic relationships among sublines of inbred mice having close relationships.

Animals↗
PubMed1993

Influence of chronic oestrogen treatment on severity of hydronephrosis in inbred DDD mice.

It has been reported that mice treated chronically with oestrogen (oestradiol propionate) increase their bladder urine volume. Since inbred DDD mice, particularly male DDD mice, lack a protective mechanism against vesicoureteral reflux (VUR), chronic oestrogen treatment may increase the pressure in the renal pelvis and lead to severe hydronephrosis. The present studies were carried out to confirm this hypothesis. Results of a least-squares analysis of variance showed that the severity of hydronephrosis was more severe after treatment with high doses of oestrogen (1.0 and 5.0 mg/kg/week) in entire and castrated male DDD mice. Hydroureter was also observed in the same groups. Intra-vesicular pressure was 7 to 12 cmH2O higher in mice of these groups than in control DDD mice. High doses of oestrogen had no effect on the kidneys of C57BL/6 mice which showed normal protection against VUR, though it increased bladder urine volume. These findings support the hypothesis that hydronephrosis in DDD mice is caused by an incomplete protective mechanism against VUR.

Animals↗
PubMed1993

Morphometric profiles of the mandible of SMXA recombinant inbred strains of mice and strain identification on the basis of mandible measurements.

SMXA recombinant inbred (RI) strains were derived from the F2 generation of a cross between two progenitor inbred strains, A/J and SM/J, which differ considerably with respect to many characters. In order to determine the morphometric profiles of the mandible of SMXA RI strains and to identify these strains, principal component and discriminant analyses (mandible analysis) were carried out using 11 mandible measurements. Principal component analysis revealed that the mandibles of each strain have their own characteristic size and shape. The RI strains, however, were roughly divided into 15 groups based on the morphometric profile of their mandibles. Discriminant analysis showed the probability of erroneous discrimination to be 6.49% (20/308) for the males and 8.06% (27/335) for the females. In both sexes, most of the erroneous discrimination (13 in the male, 17 in the female) occurred between RI strains having comparatively similar morphometric profiles. This suggested that all of the SMXA RI strains examined could be regarded as genetically homogeneous within each strain.

Animals↗
PubMed1993

Identification of inbred strains of mice and genetic relationships between strains as assessed by DNA fingerprinting.

Strain identification and the assessment of genetic relationships among inbred strains of mice were examined by DNA fingerprinting using M13 phage DNA as a probe. We used 8 inbred strains (NC/Jah, DDD/Jah, DSD/Jah, RR/Jah, SS/Jah, C3H/HeJah, C57BL/6 Jah and C57BL/6CrSlc) and coisogenic (NC-brp) as well as congenic (C57BL/6-bg) strains. DNA fingerprints using M13 phage DNA as a probe revealed identical patterns within strains. Bands due to new mutations in minisatellite regions within each strain were not observed. The banding patterns were strain-specific. Thus, DNA fingerprinting seemed to be suitable for genetic monitoring of mice. A dendrogram constructed with difference values calculated from DNA fingerprint patterns showed that relationships among strains reflected the history of these strains, so DNA fingerprinting could also be effectively used to assess the relationships between inbred strains of mice.

Animals↗
PubMed1993

[Application of DNA fingerprinting to investigation of genetic relationships between laboratory rabbit strains].

It is well known that laboratory rabbits are not controlled genetically like laboratory mice and rats. In order to test the usefulness of DNA fingerprinting in investigation of genetic uniformity of the laboratory rabbits strains and their relationships, we applied DNA fingerprinting using bacteriophage M13 probe to five strains (2 inbreds (JWY-NIBS and DuY-NIBS) and 3 outbreds (JW-NIBS, Icl:JW and WHHL)). DNA fingerprints of 2 inbred strains showed the same banding patterns within each strain but the strain-specific patterns. Although there were no rabbits showing the same banding patterns in 3 outbred strains, average percent differences (APD) were 13.7 to 18.6. A dendrogram based on APD of DNA fingerprints was constructed by 2 large clusters, JW group and DuY. The dendrogram was essentially similar to that based on rabbit mandible measurements. These results suggest that DNA fingerprinting is available not only for the genetic monitoring of the laboratory rabbit strains but also for the investigation of their genetic relationships.

Animals↗
PubMed1993

Establishment of inbred strain of long-haired golden hamster.

Features of a long-haired mutant and inheritance of mutation were investigated in the golden hamster (Mesocricetus auratus). The hair of adult long-haired hamsters was longest at the rump and flanks (approximately 70 mm) and was also unusually long at the neck (45 to 50mm). The hair length of males was more striking than that of females. Mating experiments indicated that an autosomal recessive gene is responsible for the inheritance of long hair. An albino long-haired hamster strain was established by continuous full-sib mating from F2 hybrids, descendants of (acromelanic albino x agouti long-haired) F1 progeny, and genetic homogeneity was confirmed by DNA fingerprinting. The long-haired strain was characterised by the fact that males grew larger than females, in contrast to the other strains of hamsters.

Animals↗
PubMed1991

Incomplete protection mechanism against vesico-ureteral reflux and hydronephrosis in the inbred mouse strain DDD.

We have previously reported the occurrence and inheritance mode of hydronephrosis in the inbred mouse strain DDD. The present investigation examined the possibility that hydronephrosis may be caused by a vesico-ureteral reflux (VUR). Bladder pressure was measured under anaesthesia in 3 strains of mice (DDD, ddY and C57BL/6). VUR was demonstrated by lower bladder pressure only in the DDD strain. Loading pressure into the renal pelvis (LPP) was significantly higher in DDD than in C57BL/6 (P less than 0.001). Correlations between LPP and severity of hydronephrosis were significantly positive in DDD and ddY, indicating that mice showing higher LPPs had the severest disease. Scanning electron micrography revealed that the ureteral orifice of DDD (100-300 microns) was much larger than in C57BL/6 (30 microns), and thus offered scant protection against VUR in DDD. These results suggest that DDD hydronephrosis caused by VUR is related primarily to the absence of an adequate protection mechanism in the ureteral orifice.

Animals↗
PubMed1989

Morphology of single primary vestibular afferents originating from the horizontal semicircular canal in the cat.

The central projections of physiologically characterized vestibular nerve fibers originating from the horizontal semicircular canal were studied in the vestibular nuclei of adult cats after intracellular staining with horseradish peroxidase (HRP). First, primary nerve fibers were physiologically classified as regular or irregular types on the basis of the regularity of the spontaneous discharge pattern. Then, these two types of fibers were morphologically analyzed and compared following HRP intraaxonal injection. The two types of axons showed a basically similar trajectory in the four major vestibular nuclei. They bifurcated into an ascending and a descending branch in the ventrolateral part of the lateral vestibular nucleus (LVN). The ascending branch extended rostrally and gave off one or two collaterals in the superior vestibular nucleus (SVN), although some of the ascending branches further ran rostrally into the cerebellum. The collaterals, while running medially, gave rise to fine terminal branches with en passant boutons in the SVN, and further coursing caudally, they entered the rostral part of the medial vestibular nucleus (MVN). The descending branch, while running caudally in the lateral part of the LVN and the inferior vestibular nucleus (IVN), gave off several thick collaterals to the MVN and extensive terminals were present in the IVN and MVN. In each primary axon, about one-third of the total terminal boutons were distributed in each of the SVN, the MVN, and the IVN. In contrast to this similarity of the overall axonal trajectory within the vestibular nuclei, both types of axons exhibited several marked differences in diameter and in the mode of terminal arborization. In almost every part of the ramification, the irregular-type fibers were thicker than the regular-type fibers. In the regular-type axons, many small terminal boutons (mean size, 2.4 x 1.4 microns, N = 2,739) were located in close proximity (100-150 microns) to the parent collateral. In the irregular-type axons, slightly larger terminal boutons (mean size, 3.0 x 1.7 microns, N = 1,287), were spread more widely (200-300 microns) around their collaterals. These clear morphological differences between the regular-type and the irregular-type terminal axons were consistently observed in any vestibular nucleus.

Animals↗
PubMed1989

Morphological analysis of single astrocytes of the adult cat central nervous system visualized by HRP microinjection.

The morphology of individual astrocytes of the adult cat was analyzed by HRP microinjection and light microscopy. The astrocytes had generally two types of processes: (1) thread-like processes of relatively constant width with few ramifications and few lamellar appendages and (2) the sinuous processes with clusters of lamellar appendages. The former processes were morphologically characterized as follows: (1) Those of fibrous astrocytes were frequently remarkably long, ranging from 600 to 1500 microns. They were much longer than any astrocytic processes hitherto reported in the literature. In contrast, those of protoplasmic astrocytes were usually short (30-400 microns), and were sometimes decorated with lamellae. (2) The processes often terminated in endfeet on the subpial surface of the brain tissue or on blood vessel walls. The number of endfeet per cell varied from 1-11 with a tendency to split into two populations close to each extreme number. Another type of endfoot was also found, i.e. swellings along the trunk of the processes which made side-to-side contact with the vessel wall. The sinuous processes rich in lamellae were predominant in protoplasmic astrocytes, and clearly corresponded to the sheet- or veil-like processes of Golgi-impregnated astrocytes. They formed an ellipsoidal field (100 microns for the longer, and 50-60 microns for the shorter, diameter) around the nucleus.

Animals↗
PubMed1989

Morphology of augmenting inspiratory neurons of the ventral respiratory group in the cat.

The present study examined, in Nembutal-anesthetized and artificially ventilated cats, the morphologic properties of the inspiratory neurons of the ventral respiratory group (VRG). Horseradish peroxidase (HRP) was injected into 21 augmenting inspiratory or late inspiratory neurons with peak firing rates in the late inspiratory phase. The majority of the stained neurons were antidromically activated by stimulation of the cervical cord. Thirteen somata, located within or around the nucleus ambiguus (AMB), between 100 microns caudally and 2,000 microns rostrally to the obex, were stained. In ten cases, the stem axons issuing from the cells of origin coursed medially to cross the midline without giving off any axonal collaterals. Three neurons gave rise to axonal collaterals on the ipsilateral side, distributing boutons in the medullary reticular formation, in the vicinity of the AMB, hypoglossal nucleus, solitary tract, and dorsal motor nucleus of the vagus. In eight neurons, only the axons were labeled; in four of these, which were antidromically activated from the spinal cord, the stem axons crossed the midline 2,000-3,000 microns rostral to the obex and descended in the reticular formation around the AMB down to the cervical cord. They issued several axonal collaterals, distributing terminal boutons at the level of the caudal end of the retrofacial nucleus and about 1,000 microns rostral and caudal from the obex. Terminals were found mainly in and around the AMB, and a few were found in the vicinity of the dorsal motor nucleus of the vagus. The remaining four nonactivated axons distributed their terminal boutons widely in the reticular formation around the AMB. Thus, the augmenting inspiratory neurons of the VRG were shown to project not only to the spinal cord, but also to the VRG, hypoglossal nucleus, and dorsal motor nucleus of the vagus.

Action Potentials↗
PubMed1988

Electron microscopic comparison of the terminals of two electrophysiologically distinct types of primary vestibular afferent fibers in the cat.

Two types of electrophysiologically distinct vestibular primary afferents (regular-type and irregular-type) were injected intraaxonally with HRP and their terminals were compared using the electron microscope. In general, regular-type terminals were small and two or more terminals contacted a single dendrite side by side, whereas irregular-type terminals were large and covered a wide surface of the dendrites. Both types of terminals contained spherical clear vesicles with almost the same diameter. Prominent postsynaptic membrane specializations were observed in both types. Mitochondria in both types had an elliptical profile with the same elongation index, but mitochondria in the regular-type terminals were thicker than those in the irregular-type ones.

Action Potentials↗
PubMed1987

Trajectory of group Ia and Ib fibers from the hind-limb muscles at the L3 and L4 segments of the spinal cord of the cat.

Nineteen physiologically identified group Ia and five group Ib fibers at the L3 and L4 levels of the spinal cord originating from various hind-limb muscles were intraaxonally injected with horseradish peroxidase (HRP). The trajectories of the stained axons were reconstructed. They extended for distances of 8.6 mm-18.0 mm rostrocaudally. Ascending axons ran in various regions of the dorsal funiculus: The ascending axon from a toe muscle (3 microns in diameter) ran in the ventral most part of the paramedian region; those from shank muscles (3.0-5.0 microns) in both dorsal and ventral paramedian regions; those from thigh muscles (5.0-7.0 microns) in both the paramedian and the more lateral regions; and those from hip muscles (6.0-7.0 microns) in the lateral region. Main collaterals arising from the parent fiber were given off at intervals of 0.5-6.2 mm (mean 2.4 mm). Collaterals of a fiber from a toe muscle (1.0 micron in diameter) entered Clarke's column from the dorsomedial side and ramified mostly in the dorsomedial one-third of the column. Collaterals of fibers from shank muscles (1.0-2.0 microns) entered Clarke's column from the dorsal side and terminated in its middle parts as well as in laminae V-VII. Collaterals of fibers from thigh muscles (1.0-2.5 microns) passed lateral to or through the lateral part of Clarke's column and terminated in its ventrolateral part and in laminae V-VIII. Collaterals of fibers from hip muscles (1.5-2.5 microns) passed lateral to Clarke's column and ramified mostly in laminae VII-IX. As the muscle of origin became more proximal, the proportion of termination outside of Clarke's column progressively increased. Thus, the trajectory of group I fibers was somatotopically organized both in the dorsal funiculus and in the gray matter. The long axis of boutons ranged from 0.5 to 17 microns in Ia fibers and from 0.5 to 8 microns in Ib fibers. "Giant" Ia boutons (above 7 microns) were found both in and outside Clarke's column.

Animals↗