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1.
为了解贵州威宁黄牛的遗传多样性及遗传背景,我们分析测定了19个个体线粒体DNA D-loop区序列。结果检测到8种单倍型,7种为普通牛血统的单倍型,1种为瘤牛血统的单倍型,表明威宁黄牛同时受普通牛和瘤牛的影响。本研究同时构建了19个威宁黄牛个体的系统发生树,结果发现它们明显分为普通牛血统单倍型组和瘤牛血统单倍型组两组。  相似文献   

2.
为了解贵州威宁黄牛的遗传多样性及遗传背景,测定了19个个体的线粒体DNAD-loop区全序列。威宁黄牛D-loop区全序列中,A+T平均含量为61.4%,G+C含量为38.6%。经比对,共检测到威宁黄牛D-loop区8种单倍型,核苷酸多态位点45个,其中7种为普通牛血统的单倍型,1种为瘤牛血统的单倍型,表明威宁黄牛同时受到普通牛和瘤牛的影响。在威宁黄牛19个个体中,其单倍型多样度为0.715,核苷酸歧异度(π值)为2.415%,表明威宁黄牛品种的遗传多样性丰富。  相似文献   

3.
为了研究中国黄牛Y染色体SNPs的遗传多样性及父系起源,本研究利用PCR-SSCP与测序方法,选择4个牛Y-SNPs位点DDX3Y-7、UTY-19、ZFY-9和ZFY-10,分析了16个中国地方黄牛品种284头公牛与缅甸黄牛4头公牛Y染色体的遗传多样性.结果表明,在中国16个黄牛品种中,仅发现普通牛Y2和瘤牛Y3单倍型,表明只有Y2和Y3两种父系起源,尚未发现中国黄牛存在普通牛Y1单倍型的分子证据.4头缅甸黄牛均为Y3单倍型.在中国16个黄牛品种中,Y2和Y3单倍型频率分别为57.0%和43.0%,其中Y2单倍型频率在北方黄牛中占优势(98.3%),Y3单倍型频率在南方黄牛中占优势(76.1%),中原黄牛中普通牛Y2的单倍型频率较高,为63.8%0,瘤牛Y3的单倍型频率为36.2%.本研究证明,中国黄牛存在普通牛Y2和瘤牛Y3单倍型两种父系起源,Y2单倍型频率自北向南逐渐减少,Y3单倍型频率自北向南逐渐增加,中原地区为普通牛Y2和瘤牛Y3单倍型的交汇处.  相似文献   

4.
[目的]为了探究湘西黄牛的遗传多样性与母系起源。[方法]采用PCR扩增、测序及生物信息学方法。[结果]在33头湘西黄牛mtDNA D-loop区共检测到55个变异位点,界定了15个mtDNA单倍型,单倍型多样度为0.8750,核苷酸多样度为0.0144,表明湘西黄牛的遗传多样性较低。构建的系统发育树表明湘西黄牛具有普通牛和瘤牛两大母系起源。[结论]湘西黄牛的遗传多样性较低,属于中国南方黄牛,有瘤牛和普通牛两个母系起源,受瘤牛的影响更大。  相似文献   

5.
夷陵黄牛mtDNAD-loop区遗传多样性研究   总被引:1,自引:0,他引:1  
【目的】为了探究夷陵黄牛的母系起源与遗传多样性。【方法】采用PCR扩增、测序及生物信息学方法。【结果】在27头夷陵黄牛mtDNA D-loop区共检测到54个变异位点,界定了13个mtDNA单倍型,单倍型多样度为0.7720,平均核苷酸多样度为0.0228,表明夷陵黄牛具有比较丰富的遗传多样性。构建的系统发育树显示夷陵黄牛具有普通牛和瘤牛两大母系起源。【结论】夷陵黄牛受瘤牛的影响大,属于中国南方黄牛,具有普通牛与瘤牛的种质特征。  相似文献   

6.
为研究张掖肉牛的遗传多样性及母系起源,利用特异性引物扩增mtDNA D-loop区全序列,采用最大似然法构建了张掖肉牛mtDNA D-loop区分子系统树,对核苷酸多态性和遗传距离进行了分析。结果表明,构建的166头张掖肉牛mtDNA D-loop区全序列分子系统树分为3组(普通牛、瘤牛、牦牛),其中,普通牛血统基因型组占比80.7%,有93种单倍型(Hd=0.988),核苷酸变异度π=0.005 79;瘤牛血统基因型组占比13.2%,有6种单倍型(Hd=0.476),核苷酸变异度π=0.001 19;牦牛血统基因型组占比6.1%,有5种单倍型(Hd=0.867),核苷酸变异度π=0.009 65。张掖肉牛与中国北方牛的遗传距离比较近(Fst=0.01)。综上所述,张掖肉牛具有混合母系起源的特点,但受普通牛的影响较大,亲缘关系明显表现出了中国北方黄牛的地理生态分布特征,该研究结果可为张掖肉牛生态区的分布提供理论依据,也可为遗传育种提供参考。  相似文献   

7.
摘 要:[目的]本研究旨在从基因组水平探究隆林牛和郏县红牛的线粒体DNA(mtDNA)全基因组遗传多样性与母系起源,并对2个黄牛品种的mtDNA全基因组遗传多样性进行比较分析。[方法]采用全基因组重测序及生物信息学方法。[结果]在15头隆林牛和28头郏县红牛mtDNA全基因组序列中,共检测到36种单倍型,其中郏县红牛有26种单倍型,隆林牛仅有8种单倍型,2个黄牛品种共享2种单倍型。郏县红牛和隆林牛的平均单倍型多样度(Hd)分别为1.000和0.943,平均核苷酸多样度(Pi)分别为0.0080和0.0053,表明其遗传多样性丰富。构建的系统发育树表明,隆林牛和郏县红牛具有瘤牛和普通牛两个母系支系。[结论]隆林牛以瘤牛起源为主,郏县红牛为普通牛与瘤牛的混合起源,这2个地方黄牛品种具有独特的母系遗传信息,表现出明显的母系遗传差异。  相似文献   

8.
[目的]从分子水平探究皖南牛的遗传多样性、群体遗传结构及父系起源。[方法]利用PCR产物直接测序、荧光微卫星分型方法,选择2个Y-SNPs标记(UTY-19和ZFY-10)和2个Y-STRs位点(INRA189和BM861)对35头皖南公牛进行遗传多样性检测。[结果]发现35头皖南公牛包含Y1、Y2和Y3 3种单倍型组,其频率分别为2.86%、8.56%和88.58%。普通牛Y1单倍型组只有1种单倍型(Y1-98-158),普通牛Y2单倍型组有3种单倍型(Y2-102-158、Y2-104-158和Y2-106-158),瘤牛Y3单倍型组只有1种单倍型(Y3-88-156),皖南牛Y染色体单倍型多样度为0.2185±0.0924,表明皖南牛有普通牛与瘤牛2个父系起源,遗传多样性较低。[结论]皖南牛属于南方黄牛类型,以瘤牛的种质特性为主。  相似文献   

9.
[目的] 探究云南文山牛群体Y染色体遗传结构与血统来源,以期为该黄牛品种的资源保护与利用提供科学依据。[方法] 本研究采用PCR扩增和生物信息学方法,对55头文山牛Y-SNPs(UTY19和ZFY10)和Y-STRs(INRA189和BM861)遗传多样性进行系统研究。[结果] 55头文山牛均属于瘤牛Y3单倍型组,结合Y-SNPs和Y-STRs分型结果,发现文山牛中存在Y3-88-156和Y3-90-156两种Y染色体单倍型,Y染色体单倍型多样度为0.1684±0.0636。[结论] 云南文山牛只有瘤牛父系起源,其遗传血统稳定,纯合度高。  相似文献   

10.
云南文山黄牛和迪庆黄牛的遗传多样性比较研究   总被引:1,自引:0,他引:1  
本文通过细胞遗传学、mtDNARFLP(线粒体DNA、限制性片段长度多态性)和血液蛋白及同工酶3个方面的研究,分析了云南文山黄牛和迪庆黄牛的遗传多样性和遗传分化关系。结果:(1)细胞遗传学云南两个地方黄牛品种的Y染色体形态及其C一带具有显著多态性。文山黄牛和迪庆黄牛分别为一小的近端部和亚申部(或中部)着丝位Y染色体,并分别在Y染色体的臂端部和短臂的臂端部显示弱阳性C一带,说明文山黄牛的父系起源可能是瘤牛(Bosindicus),而迪庆黄牛是普遍牛(Bostaurus)。推测两种Y染色体可能是臂问倒位的结果。(2)mtD-NARFLP两个黄牛品种的111个个体的mtDNA经8种限制性内切酶酶切后,有个酶表现出多态,共检测到17种限制性态型。归结出的3种基因单倍型,分别是A-A-A-A-A-A-A型(瘤斗)、B-B-B-B-B—B-B型(普通型)和A-C-B-B-C-A-A型(耗半Bosgrunniens)。从基因单倍型在群体中的表现可看出,文山黄牛和迪庆黄牛都具有瘤牛和普通牛两种母系起源。但文山黄牛以瘤牛血统为主,迪庆黄牛以普通牛血统为主,而且还可能含有部价耗牛的血统。(3)血液蛋白及同工酶分析了两个黄牛品种的33种血液蛋白及同工酶共计37个遗传座位,其中ALB、TF、HB一β、CAR、NP、6PGD6个座位检测到多态性。  相似文献   

11.
[目的]通过测定温岭高峰牛线粒体DNA全基因组序列以分析温岭高峰牛的母系起源及遗传多样性。[方法]采用DNA提取、测序及生物信息学方法。[结果]通过对19头温岭高峰牛线粒体DNA全基因组序列分析,共发现263个变异位点,定义9种单倍型,单倍型多样度(Hd±SD)为0.778±0.096,核苷酸多样度(Pi±SD)为0.0017±0.0014,表明温岭高峰牛的遗传多样性较低。构建的NJ系统发育树和单倍型进化网络图表明温岭高峰牛有普通牛和瘤牛2种母系起源。[结论]温岭高峰牛线粒体DNA基因组的遗传多样性较低,有瘤牛和普通牛两个母系起源,但主要受瘤牛的影响。  相似文献   

12.
[目的]研究中国黄牛Y染色体STRs的遗传多样性及父系起源。[方法]利用非变性聚丙烯酰胺凝胶电泳,选择2个牛Y-STRs位点INRA189和BM861,分析16个中国地方黄牛品种284头公牛与4头缅甸黄牛公牛的Y染色体遗传多样性。[结果]在中国16个黄牛品种中,2个Y-STR位点可以区分中国黄牛中的普通牛和瘤牛类型,表明中国黄牛有普通牛和瘤牛两种父系起源。4头缅甸黄牛均为瘤牛类型。在中国16个黄牛品种中,普通牛和瘤牛分布频率分别为57.0%和43.0%,其中普通牛频率在北方黄牛中占优势(98.3%),瘤牛频率在南方黄牛中占优势(76.1%),中原黄牛中普通牛频率较高为63.8%,瘤牛频率为36.2%。[结论]中国黄牛存在普通牛和瘤牛两种父系起源;普通牛频率自北向南逐渐减少,瘤牛频率自北向南逐渐增加,中原地区为普通牛和瘤牛的交汇处。  相似文献   

13.
The Africander has anatomical and other characteristics of an animal of approximately 3/4 Bos indicus heredity. The fact that these cattle carry the Bos taurus Y chromosome supports this view and indicates that the local cattle in South Africa would have been crossed with one or more Bos taurus bulls. Droughtmaster and Braford cattle retain the Bos indicus Y chromosome because Bos indicus instead of Bos taurus bulls were used to establish these taurindicus breeds. Contrary to some assumptions, an approximate tenfold increase in productivity of cattle was made during the 18th and 19th centuries due to improvements in disease control, nutrition and genetic improvement. What is now needed is the development of taurindicus breeds combining to the maximum possible extent the disease resistance and hardiness of Bos indicus with the early maturity and productivity of Bos taurus cattle. In addition, the ravages of disease and the seasonal variations of food supply need to be overcome in tropical areas.  相似文献   

14.
Twenty-six kidneys of 2–4 years old Bos indicus (zebu cattle) and twenty kidneys of 4-year old Bos taurus were examined under the light microscope. The renal tubular epithelial heights and diameters were smaller in zebu than in Bos taurus. The Bos indicus kidney had fewer vascular bundles in the outer medullary zone and a smaller number of capillaries per vascular bundle, hence a lower renal blood flow than in Bos taurus. The Bos indicus proximal tubules had broader brush borders than those of Bos taurus. The smaller renal corpuscles with smaller glomerular filtration surface and low renal blood flow are responsible for low glomerular filtration rate and urinary flow, enabling their kidneys to retain more water than those of Bos taurus.  相似文献   

15.
This review reveals that relative to Bos taurus cattle, cattle varying in Bos indicus inheritance, especially cattle that are > 1/2 Bos indicus inheritance, lack carcass tenderness. Because consumers are willing to pay for more tender beef, it seems imperative that the commercial beef cattle industry should refrain from producing cattle that are > 1/2 Bos indicus inheritance. Because of their Superior preweaning maternal performance, F1Bos indicus ♂ × Bos taurus 9 females and their resulting contemporary F1steer mates will continue to be produced by the commercial beef cattle industry in the Southeast and Golf Coast areas of the U.S. Further, as progeny testing for tenderness is expensive, it is suggested that the F1Bos indicus ♂ x Bos taurus 9 steers be identified by the commercial beef cattle industry so that the packing/ retail industries can utilize existing postmortem technology (electrical stimulation, blade tenderization, extended aging, calcium chloride injections) to partially alleviate the lack of tenderness expressed by carcasses resulting from these cattle.  相似文献   

16.
Twenty kidneys of 4 years old Bos taurus cattle and 26 kidneys of 2—4 years old Bos indicus (Zebu cattle) of East African Shorthorn breen were examined lobe by lobe after fixation. The cortex and medulla with subunits were measured and compared in the two sub-species. The width of the cortex was about the same in both. The outer and inner stripes of the outer medullary zone were significantly broader in Bos taurus whereas outer inner zone was significantly broader in Bos indicus. The width of the entire medulla was greater in Bos taurus.  相似文献   

17.
A cytogenetical study using metaphase chromosomes from cultured lymphocytes, was made of 2 Banteng (Bibos banteng) steers and 218 bulls representing 13 purebreeds (Bos taurus type, Bos indicus type and Sanga) and 7 cross-breeds. Studies were made of photographic karyotypes of Giemsa stained and C-banded chromosomes of bulls of each breed and of B-banded chromosomes from 3 breeds of Bos indicus and one cross-breed Australian Friesian Sahiwal) cattle. The relative lengths of chromosomes of Bos taurus and Bos indicus bulls were compared and significant difference in relative lengths of the X chromosomes were noted between these two species. There was a differences in morphology of the Y chromosomes; Sanga, Banteng and Bos taurus type breeds had a small submetacentric Y chromosome, except for the Jersey which had a metacentric Y chromosome. All Bos indicus type bulls had an acrocentric Y chromosome but the Droughtmaster breed had two forms of the Y chromosome (submetacentric and acrocentric). The C-banding patterns of the autosomes and X chromosomes were similar for all breeds while those of the Y chromosomes of Bos indicus type cattle allowed their accurate identification. G-banding patterns of Bos indicus resembled those of Bos taurus and enabled pairing of homologous chromosomes. Centromeres of the autosomes were unstained but those of the sex chromosomes were darkly stained.  相似文献   

18.
Contents: " Madura cattle," the variety found on the Indonesian island of Madura, is most often referred to as a cross between Bos javanicus and Bos indicus, based largely on phenotypic appearance. The karyotypic patterns of Madura cattle resemble those of Bos taurus, with the exception of the Y chromosome, which is of Bos indicus type. Based on what is known of Bos javanicus, it is concluded that Madura cattle could be the result of a cross between a Bos taurus or Bos javanicus cow and a Bos indicus bull .
Inhalt: Eine cytogenetische Untersuchung über das Madura-Rind
Das Madura-Rind, eine Varietät der indonesischen Insel Madura, wird wegen seines Aussehens oft als Kreuzung zwischen Bos javanicus ( Banteng) und Bos indicus ( Zebu) angesehen. Das karyotypische Bild des Madura-Rindes gleicht jenem von Bos taurus mit Ausnahme des Y-Chromosoms, welches dem Bos indicus- Typ entspricht. Nachdem, was über Bos javanicus bekannt ist, muβ man folgern, daβ das Madura-Rind ein Kreu-zungsprodukt zwischen einer Bos taurus- oder Bos javanicus-Kuh und einem Bos indi- cusBullen sein könnte .  相似文献   

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