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LincRNA#1 基因敲除单独作用不会影响牛杂合 celtic POLLED 等位基因的有角表型。

LincRNA#1 knockout alone does not affect polled phenotype in cattle heterozygous for the celtic POLLED allele.

机构信息

Department of Animal Science, University of California-Davis, Davis, CA, USA.

Department of Population Health and Reproduction, School of Veterinary Medicine, University of California-Davis, Davis, CA, USA.

出版信息

Sci Rep. 2022 May 10;12(1):7627. doi: 10.1038/s41598-022-11669-9.

Abstract

A long intergenic non-coding RNA (lincRNA#1) is overexpressed in the horn bud region of polled (hornless) bovine fetuses, suggesting a potential role in horn bud suppression. Genome editing was used to test whether the absence of this sequence was associated with the horned phenotype. Two gRNAs with high mutation efficiencies targeting the 5' and the 3' regions flanking the lincRNA#1 sequence were co-injected with Cas9 as ribonucleoprotein complexes into bovine zygotes (n = 121) 6 h post insemination. Of the resulting blastocysts (n = 31), 84% had the expected 3.7 kb deletion; of these embryos with the 3.7 kb deletions, 88% were biallelic knockouts. Thirty-nine presumptive edited 7-day blastocysts were transferred to 13 synchronized recipient cows resulting in ten pregnancies, five with embryos heterozygous for the dominant P POLLED allele at the POLLED locus, and five with the recessive pp genotype. Eight (80%) of the resulting fetuses were biallelic lincRNA#1 knockouts, with the remaining two being mosaic. RT-qPCR analysis was used to confirm the absence of lincRNA#1 expression in knockout fetuses. Phenotypic and histological analysis of the genotypically (Pp) POLLED, lincRNA#1 knockout fetuses revealed similar morphology to non-edited, control polled fetuses, indicating the absence of lincRNA#1 alone does not result in a horned phenotype.

摘要

长链非编码 RNA(lincRNA#1) 在去角(无角)牛胎儿的角芽区域过度表达,表明其在角芽抑制中可能具有潜在作用。通过基因组编辑来测试缺失该序列是否与有角表型有关。使用两种针对 lincRNA#1 序列侧翼的 5'和 3'区域具有高突变效率的 gRNA 与 Cas9 作为核糖核蛋白复合物共同注射到牛受精卵(n=121)中,在受精后 6 小时。在产生的囊胚(n=31)中,有 84%具有预期的 3.7kb 缺失;这些具有 3.7kb 缺失的胚胎中,有 88%是双等位基因敲除。39 个推定编辑的 7 天囊胚被转移到 13 只同步受体牛中,导致 10 次妊娠,其中 5 次胚胎在 POLLED 基因座处携带显性 P POLLED 等位基因杂合子,5 次胚胎携带隐性 pp 基因型。产生的 8 个(80%)胎儿是 lincRNA#1 双等位基因敲除,其余 2 个是嵌合体。RT-qPCR 分析用于确认敲除胎儿中 lincRNA#1 的表达缺失。表型和组织学分析基因型(Pp)POLLED、lincRNA#1 敲除胎儿显示出与未编辑的、对照去角胎儿相似的形态,表明单独缺失 lincRNA#1 不会导致有角表型。

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