Evidence map›Paper›PMID 41373007›Full record

ArticleBiological research2025

Development of a high-yield Rabbit line for enhanced animal pharming.

Jun Song, Dongshan Yang, Lingjie Kong, Li-Kuang Tsai, Jifeng Zhang, Y Eugene Chen, Ruby Yanru Tsai, Jie Xu

Abstract read
In one paragraph

Article in Biological research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Jun SongCenter for Advanced Models for Translational Sciences and Therapeutics, University of Michigan Medical Center, Ann Arbor, MI, 48109, USA.
Dongshan YangCenter for Advanced Models for Translational Sciences and Therapeutics, University of Michigan Medical Center, Ann Arbor, MI, 48109, USA.
Lingjie KongApplied StemCell, Inc.,, 521 Cottonwood Dr. Suite #111, Milpitas, CA, 95035, USA.
Li-Kuang TsaiCenter for Advanced Models for Translational Sciences and Therapeutics, University of Michigan Medical Center, Ann Arbor, MI, 48109, USA.
Jifeng ZhangCenter for Advanced Models for Translational Sciences and Therapeutics, University of Michigan Medical Center, Ann Arbor, MI, 48109, USA.
Y Eugene ChenCenter for Advanced Models for Translational Sciences and Therapeutics, University of Michigan Medical Center, Ann Arbor, MI, 48109, USA.
Ruby Yanru TsaiApplied StemCell, Inc.,, 521 Cottonwood Dr. Suite #111, Milpitas, CA, 95035, USA. Ruby.Tsai@appliedstemcell.com.
Jie XuCenter for Advanced Models for Translational Sciences and Therapeutics, University of Michigan Medical Center, Ann Arbor, MI, 48109, USA. jiex@umich.edu.ORCID http://orcid.org/0000-0001-9452-2878

Funding

Modernize animal pharming with emerging gene targeting technologiesR41GM110822 · NIGMS · APPLIED STEMCELL, INC. · PI XU, JIE · 2014 to 2014
$186k
NIGMS NIH HHS R41 GM110822NIGMS NIH HHS R41GM110822
6 · The paper itself

Abstract

Animal pharming involves producing recombinant protein drugs using transgenic animals. The United States Food and Drug Administration (FDA) has approved certain drugs produced in the milk of transgenic Rabbits. Traditionally, these pharming Rabbits have been developed using conventional transgenic technology, which often results in an unpredictable success rate, uncontrollable transgene insertion sites, varying copy numbers, and generally low recombinant protein yields, typically 1-2 g/L or lower. We hypothesized that utilizing the promoter of a native major milk protein gene to drive transgene expression could significantly enhance yield. To test this, we developed a rabbit line that expresses tdTomato under the control of the CSN2 gene promoter, responsible for encoding β-casein, the most abundant protein in Rabbit milk. We successfully generated knock-in founder Rabbits using CRISPR/Cas9-mediated knock-in technology, augmented by the homology-directed repair (HDR)-promoting small molecule RS-1. These founder Rabbits were able to transmit the knock-in allele to their offspring, producing both heterozygous and homozygous tdTomato knock-in Rabbits. Remarkably, the recombinant protein yield reached 15-20 g/L in the milk of homozygous animals. Our work demonstrates a promising strategy to enhance recombinant protein production in Rabbit pharming.

Indexed as

Animals, Genetically ModifiedCaseinsMilkRecombinant ProteinsAnimalsCRISPR-Cas SystemsFemaleGene Knock-In TechniquesPromoter Regions, GeneticRabbitsCaseinsRecombinant ProteinsAnimal pharmingCRISPR/Cas9CSN2 gene promoterRabbits

Identifiers

PMID41373007
PMCPMC12696889

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.