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Biomedical subjects

K Zhou

Publications and source records attributed to K Zhou.

72 records · Page 4Linked to original sources

Cloning and targeted mutations of G alpha 7 and G alpha 8, two developmentally regulated G protein alpha-subunit genes in Dictyostelium.

GTP-binding protein (G protein)-mediated signal transduction pathways play essential roles during the aggregation and differentiation process of Dictyostelium. In addition to the five known G protein alpha-subunit genes, we recently identified three novel alpha-subunit genes, G alpha 6, G alpha 7, and G alpha 8, using the polymerase chain reaction technique. We present here a more complete analysis of G alpha 7 and G alpha 8. The cDNAs of these two genes were cloned, and their complete nucleotide sequences were determined. Sequence analyses indicate that G alpha 8 possesses some unusual features. It lacks the "TCATDT" motif, a sequence of amino acids highly conserved among G alpha subunits, and has an additional 50 amino acids at its C-terminus consisting of long stretches of asparagine. Moreover, G alpha 8 is unusually resistant to protease digestion, which may indicate a slow GTP hydrolysis rate. The possible functions of these alpha-subunits were assessed by generating mutants lacking G alpha 7 or G alpha 8 by gene targeting through homologous recombination and by overexpressing G alpha 7 or G alpha 8 protein. Overexpression of G alpha 7 resulted in abnormal morphogenesis starting at the slug stage, whereas analysis of the other strains failed to reveal any obvious growth or developmental defects under either normal or stressful conditions. The implications of these results are discussed.

Amino Acid Sequence↗

DRB, DQA, DQB and DPB nucleotide sequences of Saguinus oedipus B95-8.

We present eight new nucleotide sequences derived from the second exons of class II genes within the major histocompatibility complex of Sanguinus oedipus (cotton-top tamarin). These comprise two DRB alleles (Saoe-DRB3*0504, -DRB*w1203), two DQA1 alleles (Saoe-DQA1*2501, -DQA1*2502), two DQB1 alleles (Saoe-DQB1*2201, -DQB1*2301), one DQB2 allele (Saoe-DQB2*0101) and one DPB1 allele (Saoe-DPB1*0101).

Animals↗

[Glutamyltranspeptidase (gamma-GT) activity in the serum and pharynx tissue of nasopharyngeal carcinoma patients].

The gamma-GT activity in the serum and pharynx tissue of both NPC patients (106) and pharyngitis patients (65) were detected with method of hydrolysis gamma-glutamylnitrophenylamine. The 34 NPC patient's gamma-GT were assayed both before and after radiotherapy. The results indicated that the gamma-GT activities between the NPC patients and pharyngitis patients, and the activities before and after radiotherapy have significant differences. The investigation suggests that the determination of serum and pharynx tissue gamma-GT levels of NPC patients would help to diagnose and evaluate the curative effect for NPC.

Humans↗

Biocompatibilities of organic solvents with Lactobacillus delbrueckii.

In the search for biocompatible extractants for extractive fermentation of lactic acid, the effect of twelve organic solvents on the activity of L. delbrueckii were studied at different concentration levels. On this basis, the compatibilities of twelve solvents with L. delbrueckii were summarized into four classes: completely compatible, compatible at molecular level, partially compatible and non-compatible. The characteristics were described qualitatively for each class in terms of relative values between the solubility of organic solvent in water (Cs) and the toxicity of organic solvent, which is indicated by a newly defined concentration parameter (Cm). The classification was helpful for the selection of extractant in extractive fermentation.

Fermentation↗

Indirect latex contact causes urticaria/anaphylaxis.

Recurrent urticaria/anaphylaxis is a most perplexing and critical problem, often of unknown cause. Though difficult and time consuming, identification of causes(s) can be life saving and cost saving for the patient(s). We report a complex case of urticaria/anaphylaxis induced by latex allergen in a former intensive care unit nurse, in which the allergen contact occurred remotely and indirectly by intimate contact with the spouse. Diagnosis of the latex allergy was confirmed by epicutaneous skin test in vivo as well as RAST.

Adult↗

X-ray studies reveal lanthanide binding sites at the A/B5 interface of E. coli heat labile enterotoxin.

The crystal structure determination of heat labile enterotoxin (LT) bound to two different lanthanide ions, erbium and samarium, revealed two distinct ion binding sites in the interface of the A subunit and the B pentamer of the toxin. One of the interface sites is conserved in the very similar cholera toxin sequence. These sites may be potential calcium binding sites. Erbium and samarium binding causes a change in the structure of LT: a rotation of the A1 subunit of up to two degrees relative to the B pentamer.

Bacterial Toxins↗

Nucleotide sequencing of HLA-DQ gene second exons in Chinese homozygous cells.

Six HLA class I and class II-homozygous Chinese cell lines with unique HLA-Dw types were studied. Since the majority of HLA class II nucleotide sequence polymorphism is localized within the second exons of the genes, we used the polymerase chain reaction (PCR) to amplify these regions in HLA-DQA and DQB genes and subsequently determined the nucleotide sequences. No unique DQA1 or DQB1 alleles were found. However, a new haplotype of DQA1*0601-DQB1*0301-DRB1*1202 was found in two cells; and DQA1*03011 was found in association with DR9 in another two cells. This indicates that new DR-DQ associations may explain the observed new HLA-Dw types. The DQB2 sequences were identical in all six cells and were identical to a sequence previously reported in a DR6 haplotype. The DQA2 sequences from two clones obtained from two cells differed from each other and from previously reported sequences. The results show that the DQA1 and DQB1 alleles in the Chinese individuals studied are as previously reported in Caucasian populations and as such may be typed by restriction fragment-length polymorphism (RFLP) or PCR-sequence-specific oligonucleotide typing (PCR-SSO) or PCR-RFLP using conventional probe or restriction enzyme sets.

Base Sequence↗

Ultrasonic attenuation estimation in-vivo using the difference ratio correction method.

In recent years, B scanners have been widely used clinically. Obviously, it is of particular importance to use the commercial B scanners to characterize tissue by estimating its ultrasonic attenuation in vivo. However, there are a lot of difficulties in doing so because the output of a B scanner is affected by many unknown factors. In this paper, a time domain method named the difference ratio correction (DRC) method is proposed to estimate the ultrasonic attenuation of tissue in vivo. In this method, three tissue-mimicking phantoms with known acoustical properties were employed to eliminate the instrumentation errors of the B scanner and the measuring system and to correct beam diffraction for correct attenuation estimation. Other advantages of this method are that it is very convenient to apply this method clinically and there is no need to change the inner construction of the B scanner because this method only utilizes the video output. Experimental and clinical results have proved the validity of this method.

Biophysical Phenomena↗

[Keshan disease and the selenium content of grains in Yunnan province].

The selenium content of 518 specimens of rice, wheat, maize, soybean and highland barley growing both in Keshan disease area and other places in Yunnan Province, was determined and it was found that the average selenium content of the grains in the Keshan disease area was lower than that in the other places. The selenium content of rice especially was much lower than that of wheat and soybean. The relationship of Keshan disease to the low selenium content of grains, especially rice, the most eaten grain by people in the disease area, seemed clearly established in Yunnan province as well.

Cardiomyopathies↗

Structure of yeast regulatory gene LEU3 and evidence that LEU3 itself is under general amino acid control.

Determination of the nucleotide sequence of a DNA region from Saccharomyces cerevisiae previously shown to contain the LEU3 gene revealed one long open reading frame (ORF) whose 887 codons predict the existence of a protein with a molecular mass of 100,162 daltons. The codon bias index of 0.02 suggests that LEU3 encodes a low-abundance protein. The predicted amino acid sequence contains a stretch of 31 residues near the N-terminus that is rich in cysteines and basic amino acids and shows strong homology to similar regions in five other regulatory proteins of lower eukaryotes. Additional regions with a predominance of basic amino acids are present adjacent to the cysteine-rich region. A stretch of 20 residues, 19 of which are glu or asp, is found in the carboxy terminal quarter of the protein. The 5' flanking region of LEU3 contains a TATA box 111 bp upstream from the beginning of the long ORF and two transcription initiation elements (5'TCAA3') 58 and 48 bp upstream from the ORF. The 3' flanking region shows a tripartite potential termination-polyadenylation signal. The predicted 5' and 3' ends of the transcript are in very good agreement with the previously determined size of the LEU3 message. Analysis of a LEU3'-'lacZ translational fusion suggests that the LEU3 gene, whose product is involved in the specific regulation of the leucine and possibly the isoleucine-valine pathways, is itself under general amino acid control. Consistent with this observation is the finding that the 5' flanking region of LEU3 contains two perfect copies of the general control target sequence 5'TGACTC3'.

Amino Acid Sequence↗

Distribution of rDNA in the nucleus of Giardia lamblia: detection by Ag-I silver stain.

Previous investigations have proved that diplomonads have primitive cell nuclei and lack a nucleolus. We determined the distribution of ribosomal DNA (rDNA) in diplomonad nuclei that lacked a nucleolus. Giardia lamblia was used as the experimental organism with Euglena gracilis as the control. The distribution of rDNA was demonstrated indirectly by the modified Ag-I silver technique that can indicate specifically the nucleolus organizing region (NOR) by both light and electron microscopy. In ultrathin sections of silver stained Euglena cells, all silver grains were concentrated in the fibrosa of the nucleolus, while no silver grains were found in the cytoplasm, nucleoplasm, condensed chromosomes or pars granulosa of the nucleus. In the silver stained Giardia cells, no nucleolus was found, but a few silver grains were scattered in the nucleus. This suggests that the rDNA of Giardia does not form an NOR-like structure and that its nucleus is in a primitive state.

Animals↗