赤链蛇染色体组型、C带和Ag-NORs的研究

以骨髓细胞为材料研究赤链蛇的染色体,结果表明该物种2n=46,由8对大型的和15对微小的染色体组成,AF=50.性染色体的大小介于3号和4号之间,为ZW型;8对大型染色体均显示着丝粒C带,1-6号还显示浅染端粒C带.W染色体为整条C带阳性;该物种一对NOR位于7号染色体近着丝粒区.不同地理分布群赤链蛇核型可能经历过Z与W染色体不等交换。 Abstract:The Karyotype,C-bands and Ag-NORs of Dinodon rufozonaturn (Cantor) reported is in this paper including the diploid number(2n=46)comprising 8 pairs of macro-and 15 pairs of microchromosomes,and AF=50 in the D.rufozonatum.The sex chromosome in size locates between the autochromosones No.3 and No.4,which belongs to ZW type.The C-banding technique revealed that the all macrochromosomes there are centromerc C band,the telomeric C band was only observed in Nos.1~6,while a whole W chromosome is constitutive heterochromatinization.Two NOR were observed on the pericentric of the No.7 chromosome.     

泰和乌骨鸡的核型与带型研究

采用外周血淋巴细胞培养--空气干燥法,对泰和乌骨鸡染色体核型和带型进行了研究。结果表明：泰和乌骨鸡体细胞染色体数目2n=78,染色体基本臂数AF=90,1、9号染色体及Z、W性染色体为中央着丝粒（m）染色体,2、4、7号染色体为亚中央着丝粒（sm）染色体,3、6、8、10号染色体为端着丝粒（t）染色体。G带研究表明：前10对大型染色体可分为29个区,190条带。C带处理发现,所有母鸡分裂相中W性染色体都出现C带并整条深染。Ag-NORs研究发现：Ag-NORs常定位于1、2号常染色体短臂和Z性染色体短臂端部;Ag-NORs数目分布范围为1～6;平均每个细胞的Ag-NORs数在雌、雄鸡中分别为2.94和2.96。 Abstract:This study made the chromosome slides of Taihe Silkies by the peripheral blood lymphocyte culture-drying method,and analyzed Taihe Silkies karyotype and band pattern.The results are as follow:The diploid chromosome number of Taihe Silkies was 2n=78,the basic number of chromosome arms was AF=90 and the sex chromosome type was ZZ(♂)/ZW(♀).According to the measured relative length,arm ratio and centromeric index,the first 10 pairs of macro-chromosomes are described as follows:No.1 ,9 and Z,W chromosomes were metacentrics,No.2,4,7 were submetacentrics,and No.3,6,8,10 were telocentrics.Studies on Taihe Silkies′ G-band showed that the first 10 pairs of macro-chromosomes can be divided into 29 zones and 190 bands.Being treated by C-banding technique,a totally dark-stained and easily indentified W-chromosome always showed up in the female metaphase configurations.Ag-NORs were located in the short arms′ telomere of No.1,2 euchromosomes and Z sexchromosome,the Ag-NORs number varied from 1-6. -NORs     

羊驼染色体核型及其G分带的研究

为了从选种、杂交改良、疾病诊断以及性别决定的遗传机制等方面为羊驼的繁育与推广提供更为有效的细胞遗传学资料,本试验采用外周血淋巴细胞培养法及胰酶-EDTA法分析了23只胡阿基亚型羊驼（Huacaya alpaca,雌20只,雄3只）的染色体核型及其G-分带,结果表明：羊驼二倍体染色体数目为2n=74,雄性羊驼核型为74,XY;雌性羊驼核型为74,XX。其中,1～20对常染色体为亚端着丝粒染色体,21～36对常染色体为亚中着丝粒染色体和中着丝粒染色体,X为中着丝粒染色体,Y为端着丝粒染色体。G-带分析表明,羊驼G带明暗相间,显现出不同的带纹,且羊驼每对染色体都有其独特的带纹特征,其带纹数目和精细程度随着染色体长度的增加而增加。Abstract: Blood samples from 23 Huacaya alpacas, 3 males and 20 females, were used to study chromosomes and karyotypes, so as to provide some effective cytogenetic bases for the selection, improvement by crossing, disease diagnosis of alpacas, and genetic mechanisms of sex determination. Peripheral blood lymphocyte culture was used to prepare chromosome. A method of trypase-EDTA was used for G-banding. The results showed as follows: The number of diploid chromosomes was 2n=74, with the karyotype 74, XY and 74, XX for males and females respectively. Thirty-six homologous pairs of chromosomes were autosomes, in which chromosomes pairs No.1 to No.20 were acrocentric-subterminal and No.21 to No.36 metacentric-submetacentric. And X chromosome was metacentric, Y chromosome telocentric. The analysis of G-bands showed that bright and dark bands appeared by turn. It showed different bands. And every pair of chromosomes had its distinct band, and the longer the chromosomes, the more the number of bands, and the more clear the bands.     

大鳞副泥鳅ZZ/ZW型性别决定的细胞遗传学证据

大鳞副泥鳅是鲤形目、鳅科的鱼类。其2n数为48,核型组成为12m+4sm+32 t(雄性),11m+5sm+32t(雌性)。根据银染带和C带特征分析,证实大鳞副泥鳅为ZZ/ZW型性别决定。Z染色体为中部着丝粒染色体,在其长臂端部有Ag -NOR存在。 W染色体为亚中部着丝粒染色体,在其长臂末端也有Ag-NOR存在,同时还有一深染的居间C带,这是W染色体独有的带纹特征。 Abstract:Paramisgurnus dabryanus belongs to Cypriniformes,Cobitidae.Its 2n is 48.The karyotype formula is 12m+4sm+32t(in male),11m+5sm+32t(in female).According to the Ag-NORs band and C-band patterns,we consider that its sex determination is of ZZ/ZW type.The Z chromosome is a metacentric one with Ag-NORs located on its arm end.The W chromosome is a submetacentric with Ag-NORs located on the terminal of its long arm.There is a darkly stained C-band on the long arm of W chromosome.This band is a characteric of the W chromosome.     

家燕与金腰燕染色体的比较研究

本文对家燕和金腰燕的核型、C带和Ag-NORs带进行了比较研究。结果表明,两者的核型基本一致。核型公式:2n=80=2M+4ST+zMwSM+2M+2ST+2SM+8 T+2M+56mT/D。但两者在染色体的相对长度、W染色体大小、G带带型、A g-NORs的数目和分布均存在着差异。文中在家燕No.1、7、W染色体和金腰燕No.1、 6、7染色体的形态划分,金腰燕W染色体的确定及其染色体数目等方面,均与卞小庄、李庆伟的结果不同。 Abstract:A comparative study on karyotype and C-band and Ag-NORs of house swallow and red-rumped swallow has been made.The result shows that the karyotype of them are similar,and their karyotypical formulae is 2n=80=2M+4ST+zMwSM+2M+2ST+8T+2M+56mT/D.But they are different in the relative length of chromosomes,the size of W chromosome,C-band patterns and the number and distribution of Ag-NORs.The chromosomes,the size of W chromosome,C-band patterns and the number and distribution of Ag-NORs.THE result in this paper is different from that of Mr.Bian and Mr.Li in the types of No.1,7,W chromosomes of house swallow and No.1,6,7 chromosomes of red-rumped swallow and the determination of W chromosome and diploid number of red-rumped swallow.     

赤链蛇染色体组型、C型和Ag—NORs的研究

以骨髓细胞为材料研究赤链蛇的染色体,结果表明该物种2n=46,由8对大型的和15对微小的染色体组成,AF＝50。性染色体的大小介于3号和4号之间,为ZW;8大型染色体均显示着丝粒C带,1－6号还显示浅染端粒C带。W染色体为整条C带阳性,该物种一对NOR位于7号染色体近着丝粒区。不同地理分布群赤链蛇核型可能经历过Z与W染色体不等交换。     

Physical mapping of three fruit ripening genes：Endopolygalacturonase,ACC oxidase and ACC synthase from apple（Malus x domestica） in an apple rootstock A106（Malus sieboldii

The apple rootstock,A106(Malus sieboldii),had 17 bivalents in pollen mother cells at meiotic metaphase 1,and 17 chromosomes in a haploid pollen cell.Karyotypes were prepared from root-tip cells with 2n=34 chromosomes,Seven out of 82 karyotypes(8.5%) showed one pari of satellites at the end of the short arm of chromosome 3.C-bands were shown on 6 pairs of chromosomes 2,4,6,8,14,and 16 near the telomeric regions of short arms.Probes for three ripening-related genes from Malus x domestica:endopolygalacturonase(EPG,0.6kb),ACC oxidase(1.2kb),and ACC synthase(2kb)were hybridized in situ to metaphase chromosomes of A106.Hybridization sites for the EPG gene were observed on the long arm of chromosome 14 in 15 out of 16 replicate spreads and proximal to the centromere of chromosomes 6 and 11.For the ACC oxidase gene,hylridization sites were observed in the telomeric region of the short arm of chromosomes 5 and 11 in 87% and 81% of 16 spreads respectively,proxiaml to the centromere of chromosome 1 in 81% of the spreads,and on the long arm of chromosome 13 in 50% of the spreads. Physical mapping of three fruit ripening genes in an apple rootstock A106.Twenty five spreads were studied for the ACC synthase gene and hybridization sites were observed in the telomeric region of the short arm of chromosome 12 in 96% of the spreads.chromosomes 9 and 10 in 76% of the spreads,and chromosome 17 in 56% of the spreads.     

Active expression of Gγ globin gene on chromosome 11 with Yunnanese (Ayγδβ)~0-thalasseinia deletion in MEL cells

A permanent lymphocyte cell line of a heterozygote with Yunnanese (Aγδβ)0-thalassemia deletion, associated with an increased production of Cry globin in adult, was founded using Epstein-Barr virus transformation. The hybrids of the lymphocyte cell and mouse erythroleukemia cell (MEL) were achieved and the hybrids containing human chromosome 11 were selected with the monoclonal antibody 53/6. The subclones containing only either the normal or the abnormal human chromosome 11 were separated and the expression of the human globin genes was studied. Expression of the β-globin gene, but not the Cγ and Aγ, was observed in the hybrids containing only the normal human chromosome 11, while active expression of the Cγ globin gene was observed in the hybrids containing only the abnormal human chromosome 11. These results have confirmed that the DNA deletion in the β-globin gene cluster is the cause of persistent active expression of the Cγ globin gene in the Yunnanese mutant.     

应用荧光原位杂交(FISH)技术研究 黑叶猴染色体易位

本文应用染色体荧光原位杂交(FISH)技术,利用人9号和14号染色体特异探针,对深低温冻存和长期传代的黑叶猴细胞株染色体畸变进行了分析。确定在长期冻存和传代过程中,一些黑叶猴细胞在No.12和No.17染色体之间发生了易位,一条 No.17染色体发生断裂,断裂点在17q13,断裂片段17q13-17qter易位到一条 No.12染色体长臂末端,形成一条小的中着丝粒的和一条具较长长臂的衍生染色体即 der(17) 和 der(12)。结果表明,荧光原位杂交技术用人染色体特异探针不仅能检测出人类染色体畸变,也能有效地检测灵长类动物染色体畸变。 Abstract　In this paper,the chromosome aberration of long-term cryopreserved and subcultured Francois' monkey (Semnopithecus francoisi) cell line(KCB 92008) was analyzed by fluoresence in situ hybridizaton (FISH) using human 9 and 14 chromosome DNA probes. After compared the hybridization pattern with the G-banding pattern on the same metaphase,a translocation between Nos.12 and 17 chromosomes was identified. In some Francois'monkey cells,one of chromosome No.17 was broken into two at the breakpoint 17q13,the segment(17q13-17qter) without centromere transfered to the long arm terminal of one chromosome No.12. Thus,two derivant chromosomes der(12) and der(17) were formed,the long arm of der(12) was longer than the normal partner,while the long arm of der(17) was shorter than the normal one. The result indicated that the technique of FISH using human whole chromosome probes was not only a powerful tool to detect human chromosome rearrangements,but also a usefulmethod to study the primate chromosome aberration.     

Expression of the Tribolium castaneum （Coleoptera： Tenebrionidae） hsp83 gene and its relation to oogenesis during ovarian maturation

Heat shock proteins (HSP) can protect organisms and cells from thermal damage. In this study, we cloned the full length cDNA encoding the HSP83 protein (the homologue of HSP90) of Tribolium castaneum (red flour beetle). The isolated cDNA contains the full coding sequence, a partial 5′ untranslated region of 55 bp and the complete 3′ untranslated region. We found the hsp83 gene is located on chromosome 5 of the T. castaneum genome. The predicted HSP83 protein sequence has a high similarity (on average 86.77%) with that of other insect species. The expression of the hsp83 gene in the whole body and in the ovary could be induced with heat stress (40°C for 1 h) in newly hatched (within 3 h post emergence) and mature (10 days post emergence) beetles. Under normal conditions, the hsp83 expression in the ovary is about 3-fold higher than in the whole body at both stages. No significant difference in hsp83 expression was observed between the two ovarian developmental stages regardless if the beetles were treated with heat shock or not. The expression of the HSP83 protein in the whole body could also be induced with heat stress in newly hatched and mature beetles. However, in the ovary, HSP83 was only expressed in the follicle cells of mature beetles and not in newly hatched beetles, regardless if the beetles were treated with heat shock or not. Furthermore, the females were not able to produce mature oocytes after knock-down of the hsp83 expression by injecting dsRNA. These results suggest that the HSP83 protein is involved in protection against heat stress and could be involved in oogenesis during ovarian maturation of T. castaneum.     

石貂的染色体研究

本文对分布在我国的石貂北方亚种染色体进行了较详细的研究。结果表明２ｎ＝３８,核型为１４（Ｍ）＋４（ＳＭ）＋１８（ＳＴ）,ＸＹ（Ｍ,Ａ）。Ｃ－带显示该亚种的一些染色体着丝粒区域结构异染色质弱化或消失。Ｎｏ,９染色体的短臂完全异染色质化;Ｘ染色体长臂丰出现插入杂色质带;Ｙ为完全结构异染色质组成。     

Cytogenetic characterization of the Zebra Mussel Dreissena polymorpha (Pallas) from Miedwie Lake, Poland

Cytogenetic characterization of D. polymorpha was carried out using banding techniques such as C-banding, fluorochrome CMA3 and silver nitrate treatment. The diploid chromosome number of both investigated D. polymorpha forms (typical and albinotic) was the same 2n = 32 (NF = 56). The karyotype consisted of 5 pairs of metacentric, 7 pairs of submetacentric and four pairs of subtelo-acrocentric chromosomes. Ag-NORs were located in the telomeric position on the largest subtelo-acrocentric chromosome pair. C banding patterns indicate many sites of constitutive heterochromatin mainly located in the telomeric regions and interstitially in some chromosomes. CMA3-sites were observed in almost all chromosomes; apart from the Ag-NORs sites, they were located terminally on the chromosome arms and interstitially on three chromosome pairs. Sixteen chromosomes could be counted at the diakinesis stage of meiosis. No differences in banding chromosome patterns were found neither between both analyzed forms of D. polymorpha nor between males and females.     

太平洋鳕染色体核型及银染分析

以野生太平洋鳕为材料,采用植物血球凝集素（PHA）及秋水仙素体内注射法,取头肾细胞经低渗、固定后,常规空气干燥法制备染色体标本,并对其染色体核型进行了分析。结果表明,太平洋鳕的二倍体染色体数目为2n=46,核型公式为:2n=8m+6sm+20st+12t,NF=60,即有4对中部着丝点染色体、3对亚中部着丝点染色体、10对亚端部着丝点染色体和6对端位着丝点染色体,染色体臂数为NF=60;染色体经银染后,Ag-NORs在不同间期细胞中表现出多态性,数目为13,其中2个Ag-NORs的频率最高（82%）;在分裂相中,具有1个Ag-NORs的频率最高（87.1%）,且在第12对亚端部着丝点染色体的一条带有明显的次缢痕,为Ag-NORs所在区域,并未发现Ag-NORs联合现象及性别相关的异型染色体。       

Cytogenetic variation in farmed stock of Dybowski's sika deer

The chromosome constitution of Dybowski's sika deer was studied on the basis of 15 samples obtained from farmed stock maintained in an enclosure. The diploid chromosome number was 2n=68, 2n=67 and 2n=66. The constitutive heterochromatin (C-bands) was located in the centromeric regions of all acrocentric chromosomes. Metacentric chromosomes were C-negative. Chromosomes of three pairs proved to be NORs carriers. The size polymorphism of silver deposits was identified in two animals. A cytogenetic analysis indicated that the farmed stock of Dybowski's sika deer demonstrates considerable variation. The chromosome polymorphism observed may be a valuable marker for the management and preservation of this species.     

The karyotype of the South American rodent Kunsia tomentosus (Lichtenstein, 1830).

Chromosomal analysis of Kunsia tomentosus showed a karyotype with 2n = 44, constituted by 21 pairs of acrocentric autosomes. The X chromosome was a median acrocentric, between pairs 3 and 4 in size, and the Y chromosome was a small acrocentric (between pairs 19 and 20). Five pairs with nucleolus organizer regions were located at the short arms. C-banding showed blocks of constitutive heterochromatin occurring in the centromeres of all autosomes and of the X chromosome. The Y chromosome was entirely heterochromatic. In order to identify possible homologies, karyotypes of Kunsia and Scapteromys, the phyletically related taxa, were compared. No autosome shared by either genus was found by G-band comparisons. The C-band patterns and those produced by Alu I, Mbo I, Rsa I and Hae III restriction endonucleases were also different. The results of FISH indicated a different composition of the telomeric regions of the chromosomes of both taxa, since in Scapteromys the probes hybridized in both telomeres, and in Kunsia this hybridization only occurred in one of the telomeres. These differences also occurred in the localization and number of nucleolus organizer regions.     

黑线姬鼠华北亚种染色体研究

本文采用骨髓染色体制片法,对分布于山东的黑线姬鼠华北亚种的染色体组型,C-带、G-带和银染核型进行了分析研究。其核型为2n=48=38 T+8 M+XY。X为较小的端着丝粒染色体,Y为组型中最大的染色体。几乎每个常染色体的着丝粒区都具异染色质。性染色体的异染色质丰富。No.10和No.18染色体具NOR(?)。每条染色体都显示出较清晰的G-带。同时对黑线姬鼠精母细胞的减数分裂进行了观察,并将山东标本与欧洲标本的核型进行了比较,其性染色体有显著差异。     

中国刺猬的染色体研究

本文采用全血培养和骨髓染色体制片法,对分布于我国南京市郊和济南市郊的刺猬染色体进行了组型、C-带、G-带和银染色的观察分析,并与东欧、西欧两种刺猬比较,它们之间的核型及带型差异显著;又将南京、济南及金清波(1985)报道的河南新乡三地分布的刺猬进行比较,它们的核型及带型也显示出一定差异,这种多态性在分类和进化上有一定的意义。     

黑斑蛙核型、C-带及Ag-NORs 研究

本文采用外周血淋巴细胞培养法制备染色体标本,观察黑斑蛙的染色体标本,研究黑斑蛙的核型,C-带和Ag-NORs。研究结果表明：（1）黑斑蛙淋巴细胞染色体数目为2n=26,其中有5对大染色体和8对小染色体,核型是二型性核型;（2）分别对雌雄个体的中期分裂相进行观察,在第11号染色体长臂中部有明显的次缢痕,但变异核型次缢痕在第8号染色体长臂的中部;（3）在第5号染色体长臂上有一条明显的近端粒C-带;（4）第11号染色体是一对具有银染核仁形成区的同源染色体,且雌雄个体的银染位置相同。     

辽宁产粗皮蛙的染色体组型研究(图版Ⅳ,下)

用骨髓细胞制片法分析了粗皮蛙的染色体组型 ,结果表明其二倍体染色体数为 2 6 ,可配成 13对 ,有5对大型染色体 (相对长度 >9)和 8对小型染色体 (相对长度 <6 5 ) ,其中 ,第 1、 5、 6、 7、 8对为中部着丝点染色体 ,第 12对为端部着丝点染色体 ,第 2、 3、 4、 9、 10、 11、 13对为亚中部着丝点染色体 ,第 4对为性染色体 ,属XY型 ,X染色体为亚中部着丝点 (相对长度为 10 70 ,臂比指数为 1 72 ) ,Y染色体为亚中部着丝点(相对长度为 12 83,臂比指数为 2 0 2 )。     

Cytogenetic study on Microtus guentheri (Danford and Alston, 1880) (mammalia: rodentia) from Turkey: constitutive heterochromatin distribution and nucleolar organizer regions

Conventionally stained, C- and Ag-NOR banded karyotypes of Guenther's vole, Microtus guentheri were studied from Turkey. The species possesses a karyotype of 2n = 54, NFa = 52 and NF = 54 in specimens from Kahramanmara? and Gaziantep provinces, whereas NF = 56 in females and NF = 55 in males were found in individuals from Kirikkale and Nev?ehir provinces. The X chromosome was a large acrocentric (NF = 54) or submetacentric (NF = 55, 56) while the Y chromosome was a small telocentric in all specimens examined. Blocks of constitutive heterochromatin were located in the pericentromeric areas of autosomes including the X chromosome. Nucleolar organizer regions (NORs) were located at the telomeric regions of the short arms of five acrocentric pairs and centromeric regions of two telocentric pairs in the Nev?ehir and Kirikkale specimens.