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Aberrant expression of imprinted genes and their regulatory network in cloned cattle

机译:印迹基因在克隆牛中的异常表达及其调控网络

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Domesticated animals cloned by somatic cell nuclear transfer (SCNT) generally have poor developmental competency, with many developmental abnormalities attributed to incomplete reprogramming of the nuclear genome and abnormal expression of genes important for regulation of growth and development. To investigate the molecular mechanism leading to the abnormalities of cloned animals, pathologic and histologic analyses were conducted on seven cloned cattle that were oversized at birth and had cardiac and pulmonary abnormalities. Quantitative reverse transcription (RT)-polymerase chain reaction (PCR) analysis of four imprinted genes IGF2, IGF2R, H19, and GRB10, as well as genes from related regulatory networks, were performed in liver, lung, kidney, and muscle to investigate disruption of expression. Expression of IGFBP2 was not detected in morphologically normal cloned cattle, but was detected in the liver, lung, kidney, and thymus of abnormal calves. Expression levels of IGF1 and imprinted genes IGF2 and H19 were substantially higher in these organs of abnormal cattle. In contrast, expression levels of GRB10, CTSD, and TRPV2 were substantially lower in abnormal cattle. Transcript abundance of IGFBP6 was higher in kidney, but lower in liver and lung. In conclusion, we inferred that altered expression of imprinted and related genes may be closely related to increased birth weight and pathologic changes in abnormal cloned cattle
机译:通过体细胞核移植(SCNT)克隆的家养动物通常发育能力差,许多发育异常归因于核基因组的不完全重编程以及对调节生长和发育很重要的基因的异常表达。为了研究导致克隆动物异常的分子机制,对7头出生时超大并患有心脏和肺部异常的克隆牛进行了病理和组织学分析。在肝,肺,肾和肌肉中对四个印迹基因IGF2,IGF2R,H19和GRB10以及相关调控网络的基因进行了定量逆转录(RT)-聚合酶链反应(PCR)分析表达。在形态正常的克隆牛中未检测到IGFBP2的表达,但在异常犊牛的肝,肺,肾和胸腺中检测到了IGFBP2的表达。在这些异常牛的这些器官中,IGF1以及印记的基因IGF2和H19的表达水平明显更高。相反,异常牛的GRB10,CTSD和TRPV2的表达水平明显较低。 IGFBP6的转录本丰度在肾脏中较高,但在肝和肺中较低。总之,我们推断印迹基因和相关基因的表达改变可能与异常克隆牛的出生体重增加和病理变化密切相关。

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